Infections caused by bacteria and fungi, general, specified, or unspecified.
Superficial infections of the skin or its appendages by any of various fungi.
Infection with a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES. It is sometimes called valley fever but should not be confused with RIFT VALLEY FEVER. Infection is caused by inhalation of airborne, fungal particles known as arthroconidia, a form of FUNGAL SPORES. A primary form is an acute, benign, self-limited respiratory infection. A secondary form is a virulent, severe, chronic, progressive granulomatous disease with systemic involvement. It can be detected by use of COCCIDIOIDIN.
Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues.
Scaly papule or warty growth, caused by five fungi, that spreads as a result of satellite lesions affecting the foot or leg. The extremity may become swollen and, at its distal portion, covered with various nodular, tumorous, verrucous lesions that resemble cauliflower. In rare instances, the disease may begin on the hand or wrist and involve the entire upper extremity. (Arnold, Odom, and James, Andrew's Diseases of the Skin, 8th ed, p362)
Infection resulting from inhalation or ingestion of spores of the fungus of the genus HISTOPLASMA, species H. capsulatum. It is worldwide in distribution and particularly common in the midwestern United States. (From Dorland, 27th ed)
A fungal infection that may appear in two forms: 1, a primary lesion characterized by the formation of a small cutaneous nodule and small nodules along the lymphatics that may heal within several months; and 2, chronic granulomatous lesions characterized by thick crusts, warty growths, and unusual vascularity and infection in the middle or upper lobes of the lung.
A mycosis affecting the skin, mucous membranes, lymph nodes, and internal organs. It is caused by Paracoccidioides brasiliensis. It is also called paracoccidioidal granuloma. Superficial resemblance of P. brasiliensis to Blastomyces brasiliensis (BLASTOMYCES) may cause misdiagnosis.
A family of ascomycetous fungi, order Onygenales, characterized by smooth ascospores. Genera in the family include Arthroderma, Keratinomyces, and Ctenomyces. Several well-known anamorphic forms are parasitic upon the skin.
The commonest and least serious of the deep mycoses, characterized by nodular lesions of the cutaneous and subcutaneous tissues. It is caused by inhalation of contaminated dust or by infection of a wound.
Infections with fungi of the genus ASPERGILLUS.
Infection in humans and animals caused by fungi in the class Zygomycetes. It includes MUCORMYCOSIS and entomophthoramycosis. The latter is a tropical infection of subcutaneous tissue or paranasal sinuses caused by fungi in the order Entomophthorales. Phycomycosis, closely related to zygomycosis, describes infection with members of Phycomycetes, an obsolete classification.
Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed)
Lung infections with the invasive forms of ASPERGILLUS, usually after surgery, transplantation, prolonged NEUTROPENIA or treatment with high-doses of CORTICOSTEROIDS. Invasive pulmonary aspergillosis can progress to CHRONIC NECROTIZING PULMONARY ASPERGILLOSIS or hematogenous spread to other organs.
An imidazole antifungal agent that is used topically and by intravenous infusion.
Macrolide antifungal antibiotic produced by Streptomyces nodosus obtained from soil of the Orinoco river region of Venezuela.
A kingdom of eukaryotic, heterotrophic organisms that live parasitically as saprobes, including MUSHROOMS; YEASTS; smuts, molds, etc. They reproduce either sexually or asexually, and have life cycles that range from simple to complex. Filamentous fungi, commonly known as molds, refer to those that grow as multicellular colonies.
Meningitis caused by fungal agents which may occur as OPPORTUNISTIC INFECTIONS or arise in immunocompetent hosts.
Substances of fungal origin that have antigenic activity.
A triazole antifungal agent that inhibits cytochrome P-450-dependent enzymes required for ERGOSTEROL synthesis.
An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression.
Infection with a fungus of the species CRYPTOCOCCUS NEOFORMANS.
A mitosporic fungal genus and an anamorphic form of Arthroderma. Various species attack the skin, nails, and hair.
A genus of yeast-like mitosporic Saccharomycetales fungi characterized by producing yeast cells, mycelia, pseudomycelia, and blastophores. It is commonly part of the normal flora of the skin, mouth, intestinal tract, and vagina, but can cause a variety of infections, including CANDIDIASIS; ONYCHOMYCOSIS; vulvovaginal candidiasis (CANDIDIASIS, VULVOVAGINAL), and thrush (see CANDIDIASIS, ORAL). (From Dorland, 28th ed)
A chronic progressive subcutaneous infection caused by species of fungi (eumycetoma), or actinomycetes (actinomycetoma). It is characterized by tumefaction, abscesses, and tumor-like granules representing microcolonies of pathogens, such as MADURELLA fungi and bacteria ACTINOMYCETES, with different grain colors.
A mitosporic Ophiostomataceae fungal genus, whose species Sporothrix schenckii is a well-known animal pathogen. The conidia of this soil fungus may be inhaled causing a primary lung infection, or may infect independently via skin punctures.
Triazole antifungal agent that is used to treat oropharyngeal CANDIDIASIS and cryptococcal MENINGITIS in AIDS.
A mitosporic fungal genus which causes COCCIDIOIDOMYCOSIS.
A mitosporic fungal genus causing opportunistic infections, endocarditis, fungemia, a hypersensitivity pneumonitis (see TRICHOSPORONOSIS) and white PIEDRA.
A mitosporic fungal genus. P. brasiliensis (previously Blastomyces brasiliensis) is the etiologic agent of PARACOCCIDIOIDOMYCOSIS.
A fungal infection of the nail, usually caused by DERMATOPHYTES; YEASTS; or nondermatophyte MOLDS.
Immunoglobulins produced in a response to FUNGAL ANTIGENS.
A genus of mitosporic fungi containing about 100 species and eleven different teleomorphs in the family Trichocomaceae.
Polysaccharides consisting of mannose units.
Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus.
A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
Pulmonary diseases caused by fungal infections, usually through hematogenous spread.
The study of the structure, growth, function, genetics, and reproduction of fungi, and MYCOSES.
A human or animal whose immunologic mechanism is deficient because of an immunodeficiency disorder or other disease or as the result of the administration of immunosuppressive drugs or radiation.
A fluorinated cytosine analog that is used as an antifungal agent.
A mitosporic Onygenales fungal genus causing HISTOPLASMOSIS in humans and animals. Its single species is Histoplasma capsulatum which has two varieties: H. capsulatum var. capsulatum and H. capsulatum var. duboisii. Its teleomorph is AJELLOMYCES capsulatus.
Glucose polymers consisting of a backbone of beta(1->3)-linked beta-D-glucopyranosyl units with beta(1->6) linked side chains of various lengths. They are a major component of the CELL WALL of organisms and of soluble DIETARY FIBER.
Meningeal inflammation produced by CRYPTOCOCCUS NEOFORMANS, an encapsulated yeast that tends to infect individuals with ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunocompromised states. The organism enters the body through the respiratory tract, but symptomatic infections are usually limited to the lungs and nervous system. The organism may also produce parenchymal brain lesions (torulomas). Clinically, the course is subacute and may feature HEADACHE; NAUSEA; PHOTOPHOBIA; focal neurologic deficits; SEIZURES; cranial neuropathies; and HYDROCEPHALUS. (From Adams et al., Principles of Neurology, 6th ed, pp721-2)
The constant presence of diseases or infectious agents within a given geographic area or population group. It may also refer to the usual prevalence of a given disease with such area or group. It includes holoendemic and hyperendemic diseases. A holoendemic disease is one for which a high prevalent level of infection begins early in life and affects most of the child population, leading to a state of equilibrium such that the adult population shows evidence of the disease much less commonly than do children (malaria in many communities is a holoendemic disease). A hyperendemic disease is one that is constantly present at a high incidence and/or prevalence rate and affects all groups equally. (Last, A Dictionary of Epidemiology, 3d ed, p53, 78, 80)
Cyclic hexapeptides of proline-ornithine-threonine-proline-threonine-serine. The cyclization with a single non-peptide bond can lead them to be incorrectly called DEPSIPEPTIDES, but the echinocandins lack ester links. Antifungal activity is via inhibition of 1,3-beta-glucan synthase production of BETA-GLUCANS.
The intergenic DNA segments that are between the ribosomal RNA genes (internal transcribed spacers) and between the tandemly repeated units of rDNA (external transcribed spacers and nontranscribed spacers).
Postmortem examination of the body.
A species of imperfect fungi from which the antibiotic fumigatin is obtained. Its spores may cause respiratory infection in birds and mammals.
Deoxyribonucleic acid that makes up the genetic material of fungi.
A species of the fungus CRYPTOCOCCUS. Its teleomorph is Filobasidiella neoformans.
A decrease in the number of NEUTROPHILS found in the blood.
Neoplasms located in the blood and blood-forming tissue (the bone marrow and lymphatic tissue). The commonest forms are the various types of LEUKEMIA, of LYMPHOMA, and of the progressive, life-threatening forms of the MYELODYSPLASTIC SYNDROMES.
Any tests that demonstrate the relative efficacy of different chemotherapeutic agents against specific microorganisms (i.e., bacteria, fungi, viruses).
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)

Treatment of murine fusariosis with SCH 56592. (1/2265)

Doses of 10 to 100 mg of the azole antifungal agent SCH 5692/kg of body weight/day were studied in immunocompetent mice as therapy for systemic infection by Fusarium solani. Treatment was begun 1 h after intravenous infection and continued daily for 4 or 13 doses. Prolongation of survival and organ clearance were dependent on both the dose and the duration of SCH 56592 therapy, with the best results seen at 50 and 100 mg/kg/day. The results at the highest doses of SCH 56592 used (50 or 100 mg/kg/day) were comparable to those obtained with amphotericin B at 1 mg/kg/day. SCH 56592 has potential for therapy of systemic infections caused by F. solani.  (+info)

In-vitro activity of voriconazole, itraconazole and amphotericin B against filamentous fungi. (2/2265)

The in-vitro fungistatic and fungicidal activities of voriconazole were compared with those of itraconazole and amphotericin B. MICs for 110 isolates belonging to 11 species of filamentous fungi were determined by a broth microdilution adaptation of the method recommended by the National Committee for Clinical Laboratory Standards. Minimum lethal concentrations (MLCs) of the three antifungal agents were also determined. The MIC ranges of the three compounds were comparable for Aspergillus flavus, Aspergillus fumigatus, Cladophialophora bantiana and Exophiala dermatitidis. Voriconazole and itraconazole were more active than amphotericin B against Fonsecaea pedrosoi, but the two azole agents were less active against Sporothrix schenckii. Voriconazole was more active than itraconazole or amphotericin B against Scedosporium apiospermum, but less active than the other two agents against two mucoraceous moulds, Absidia corymbifera and Rhizopus arrhizus. Voriconazole and amphotericin B were more active than itraconazole against Fusarium solani. With the exception of S. apiospermum, all the moulds tested had MLC50 values of < or =2 mg/L and MLC90 values of < or =4 mg/L against amphotericin B. Voriconazole and itraconazole showed fungicidal effects against five of the 1 1 moulds tested (A. flavus, A. fumigatus, C. bantiana, E. dermatitidis and F. pedrosoi) with MLC90 values of < or =2 mg/L. In addition, voriconazole was fungicidal for Phialophora parasitica. Our results suggest that voriconazole could be effective against a wide range of mould infections in humans.  (+info)

In-vivo therapeutic efficacy in experimental murine mycoses of a new formulation of deoxycholate-amphotericin B obtained by mild heating. (3/2265)

Heat-induced 'superaggregation' of deoxycholate-amphotericin B (AmB-DOC, Fungizone) was shown previously to reduce the in-vitro toxicity of this antifungal agent. We compared AmB-DOC with the formulation obtained by heating the commercial form (Fungizone, Bristol Myers Squibb, Paris, France) for 20 min at 70 degrees C, in the treatment of murine infections. An improvement of antifungal activity was obtained with heated AmB-DOC formulations due to a lower toxicity which allowed the administration of higher drug doses than those achievable with the commercial preparation. Single intravenous injections of heated AmB-DOC solutions were demonstrated to be two-fold less toxic than unheated ones to healthy mice. For mice infected with Candida albicans, the maximum tolerated dose was higher with heated than with unheated AmB-DOC solutions. In the model of murine candidiasis, following a single dose of heated AmB-DOC 0.5 mg/kg, 85% of mice survived for 3 weeks, whereas at this dose the immediate toxicity of the standard formulation in infected mice restricted the therapeutic efficacy to 25% survival. Both formulations were equally effective in increasing the survival time for murine cryptococcal pneumonia and meningoencephalitis. Injection of heated AmB-DOC solutions at a dose two-fold higher than the maximal tolerated dose observed with the unheated preparation (1.2 mg/kg) increased the survival time by a factor of 1.4 in cryptococcal meningoencephalitis. These results indicate that mild heat treatment of AmB-DOC solutions could provide a simple and economical method to improve the therapeutic index of this antifungal agent by reducing its toxicity on mammalian cells.  (+info)

Itraconazole oral solution as prophylaxis for fungal infections in neutropenic patients with hematologic malignancies: a randomized, placebo-controlled, double-blind, multicenter trial. GIMEMA Infection Program. Gruppo Italiano Malattie Ematologiche dell' Adulto. (4/2265)

To evaluate the efficacy and safety of itraconazole oral solution for preventing fungal infections, a randomized, placebo-controlled, double-blind, multicenter trial was conducted: 405 neutropenic patients with hematologic malignancies were randomly assigned to receive either itraconazole, 2.5 mg/kg every 12 hours (201 patients), or placebo (204 patients). Proven and suspected deep fungal infection occurred in 24% of itraconazole recipients and in 33% of placebo recipients, a difference of 9 percentage points (95% confidence interval [CI], 0.6% to 22.5%; P = .035). Fungemia due to Candida species was documented in 0.5% of itraconazole recipients and in 4% of placebo recipients, a difference of 3.5 percentage points (95% CI, 0.5% to 6%; P = .01). Deaths due to candidemia occurred in none of the itraconazole recipients compared with 4 placebo recipients, a difference of 2 percentage points (95% CI, 0.05% to 4%; P = .06). Aspergillus infection was documented in four itraconazole recipients (one death) and one placebo recipient (one death). Side effects causing drug interruption occurred in 18% of itraconazole recipients and 13% of placebo recipients. Itraconazole oral solution was well-tolerated and effectively prevented proven and suspected deep fungal infection as well as systemic infection and death due to Candida species.  (+info)

Randomized placebo-controlled trial of fluconazole prophylaxis for neutropenic cancer patients: benefit based on purpose and intensity of cytotoxic therapy. The Canadian Fluconazole Prophylaxis Study Group. (5/2265)

A randomized, double-blind trial comparing oral fluconazole (400 mg daily) with placebo as prophylaxis for adult patients receiving intensive cytotoxic therapy for acute leukemia or autologous bone marrow transplantation was conducted in 14 Canadian university-affiliated hospitals. Although fluconazole prophylaxis did not obviate the need for parenteral antifungal therapy compared with placebo (81 [57%] of 141 vs. 67 [50%] of 133, respectively), its use resulted in fewer superficial fungal infections (10 [7%] of 141 vs. 23 [18%] of 131, respectively; P = .02) and fewer definite and probable invasive fungal infections (9 vs. 32, respectively; P = .0001). Fluconazole recipients had fewer deaths attributable to definite invasive fungal infection (1 of 15 vs. 6 of 15, respectively; P = .04) and achieved more frequent success without fungal colonization (52 [37%] of 141 vs. 27 [20%] of 133, respectively; P = .004; relative risk reduction, 85%) than did placebo recipients. Patients benefiting the most from fluconazole prophylaxis included those with acute myeloid leukemia who were undergoing induction therapy with cytarabine plus anthracycline-based regimens and those receiving marrow autografts not supported with hematopoietic growth factors. Fluconazole prophylaxis reduces the incidence of superficial fungal infection and invasive fungal infection and fungal infection-related mortality among patients who are receiving intensive cytotoxic chemotherapy for remission induction.  (+info)

Phycomycotic gastritis in buffalo calves (Bubalis bubalis). (6/2265)

Mycotic gastritis, primarily caused by Rhizopus sp. was seen in six buffalo calves (7-13 days old) at postmortem examination. The predominant lesions were numerous raised ulcers in which were hyphae of Rhizopus. In three calves, Candida organisms were also present superficially in the ulcers. Other changes in the mucosa were severe congestion, haemorrhage, thrombosis, necrosis, and infiltration by lymphocytes and neutrophils. Both Rhizopus and Candida were highly pathogenic to rabbits when inoculated intravenously. The disease could not be reproduced experimentally by feeding of Rhizopus orally to rabbits and calves.  (+info)

Liposomal amphotericin B for empirical therapy in patients with persistent fever and neutropenia. National Institute of Allergy and Infectious Diseases Mycoses Study Group. (7/2265)

BACKGROUND: In patients with persistent fever and neutropenia, amphotericin B is administered empirically for the early treatment and prevention of clinically occult invasive fungal infections. However, breakthrough fungal infections can develop despite treatment, and amphotericin B has substantial toxicity. METHODS: We conducted a randomized, double-blind, multicenter trial comparing liposomal amphotericin B with conventional amphotericin B as empirical antifungal therapy. RESULTS: The mean duration of therapy was 10.8 days for liposomal amphotericin B (343 patients) and 10.3 days for conventional amphotericin B (344 patients). The composite rates of successful treatment were similar (50 percent for liposomal amphotericin B and 49 percent for conventional amphotericin B) and were independent of the use of antifungal prophylaxis or colony-stimulating factors. The outcomes were similar with liposomal amphotericin B and conventional amphotericin B with respect to survival (93 percent and 90 percent, respectively), resolution of fever (58 percent and 58 percent), and discontinuation of the study drug because of toxic effects or lack of efficacy (14 percent and 19 percent). There were fewer proved breakthrough fungal infections among patients treated with liposomal amphotericin B (11 patients [3.2 percent]) than among those treated with conventional amphotericin B (27 patients [7.8 percent], P=0.009). With the liposomal preparation significantly fewer patients had infusion-related fever (17 percent vs. 44 percent), chills or rigors (18 percent vs. 54 percent), and other reactions, including hypotension, hypertension, and hypoxia. Nephrotoxic effects (defined by a serum creatinine level two times the upper limit of normal) were significantly less frequent among patients treated with liposomal amphotericin B (19 percent) than among those treated with conventional amphotericin B (34 percent, P<0.001). CONCLUSIONS: Liposomal amphotericin B is as effective as conventional amphotericin B for empirical antifungal therapy in patients with fever and neutropenia, and it is associated with fewer breakthrough fungal infections, less infusion-related toxicity, and less nephrotoxicity.  (+info)

Detection of cell wall mannoprotein Mp1p in culture supernatants of Penicillium marneffei and in sera of penicilliosis patients. (8/2265)

Mannoproteins are important and abundant structural components of fungal cell walls. The MP1 gene encodes a cell wall mannoprotein of the pathogenic fungus Penicillium marneffei. In the present study, we show that Mp1p is secreted into the cell culture supernatant at a level that can be detected by Western blotting. A sensitive enzyme-linked immunosorbent assay (ELISA) developed with antibodies against Mp1p was capable of detecting this protein from the cell culture supernatant of P. marneffei at 10(4) cells/ml. The anti-Mp1p antibody is specific since it fails to react with any protein-form lysates of Candida albicans, Histoplasma capsulatum, or Cryptococcus neoformans by Western blotting. In addition, this Mp1p antigen-based ELISA is also specific for P. marneffei since the cell culture supernatants of the other three fungi gave negative results. Finally, a clinical evaluation of sera from penicilliosis patients indicates that 17 of 26 (65%) patients are Mp1p antigen test positive. Furthermore, a Mp1p antibody test was performed with these serum specimens. The combined antibody and antigen tests for P. marneffei carry a sensitive of 88% (23 of 26), with a positive predictive value of 100% and a negative predictive value of 96%. The specificities of the tests are high since none of the 85 control sera was positive by either test.  (+info)

The most common types of mycoses include:

1. Ringworm: This is a common fungal infection that causes a ring-shaped rash on the skin. It can affect any part of the body, including the arms, legs, torso, and face.
2. Athlete's foot: This is a common fungal infection that affects the feet, causing itching, redness, and cracking of the skin.
3. Jock itch: This is a fungal infection that affects the groin area and inner thighs, causing itching, redness, and cracking of the skin.
4. Candidiasis: This is a fungal infection caused by Candida, a type of yeast. It can affect various parts of the body, including the mouth, throat, and vagina.
5. Aspergillosis: This is a serious fungal infection that can affect various parts of the body, including the lungs, sinuses, and brain.

Symptoms of mycoses can vary depending on the type of infection and the severity of the infection. Common symptoms include itching, redness, swelling, and cracking of the skin. Treatment for mycoses usually involves antifungal medications, which can be applied topically or taken orally. In severe cases, hospitalization may be necessary to monitor and treat the infection.

Preventive measures for mycoses include practicing good hygiene, avoiding sharing personal items such as towels and clothing, and using antifungal medications as prescribed by a healthcare professional. Early diagnosis and treatment of mycoses can help prevent complications and reduce the risk of transmission to others.

These types of infections can be mild or severe and can have a significant impact on public health. For example, tuberculosis is a bacterial infection that affects the lungs and can be transmitted through airborne droplets, while candidiasis is a fungal infection that can affect various parts of the body, including the skin, mouth, and vagina.

Bacterial infections and mycoses can be treated with antibiotics or antifungal medications, but some types of infections can be resistant to treatment, making them difficult to manage. It is important to identify the specific cause of an infection and to take appropriate steps to prevent its spread, such as practicing good hygiene, avoiding close contact with people who are sick, and following proper infection control procedures in healthcare settings.

Prevention and Control:

1. Practice good hygiene: Wash your hands frequently, especially after using the bathroom or before eating.

2. Avoid close contact with people who are sick: Keep a distance from people who have infections, especially if they have a contagious infection like tuberculosis or strep throat.

3. Follow proper infection control procedures in healthcare settings: Healthcare providers should follow strict infection control guidelines when caring for patients with infections, including wearing gloves and masks, cleaning equipment and surfaces thoroughly, and properly disposing of medical waste.

4. Get vaccinated: Vaccines can help prevent some types of bacterial infections, such as pneumococcal disease and Haemophilus influenzae type b (Hib) disease.

5. Use antibiotics wisely: Antibiotics should only be used to treat bacterial infections, not viral infections. Overuse or misuse of antibiotics can lead to the development of drug-resistant bacteria, making infections harder to treat.

6. Practice safe sex: Using condoms and other forms of barrier protection can help prevent the spread of some types of infections, such as chlamydia and gonorrhea.

7. Avoid sharing personal items: Sharing personal items, such as towels or drinking glasses, can spread infections from one person to another.

8. Properly store and prepare food: Improper food storage and preparation can lead to the growth of harmful bacteria, such as E. coli and Salmonella.

9. Keep wounds clean and covered: Properly cleaning and covering wounds can help prevent infection and promote healing.

10. Get regular check-ups: Regular health check-ups can help identify infections early, when they are easier to treat.

By following these steps, you can help prevent the spread of bacterial infections and keep yourself and others healthy. It's important to remember that not all infections can be prevented, but taking these precautions can greatly reduce your risk of getting sick.

Also found in: Medical, Encyclopedia.

Examples from the web for 'dermatomycoses'

Some common types of dermatomycoses include athlete's foot and jock itch.

Scientific American, 25 Mar. 2019.

Topical antifungal medications are effective against most types of dermatomycoses.

Britannica.com: encyclopedia article about dermatomycoses.

This condition is caused by a type of fungus that affects the skin, known as dermatomycoses.

Mayo Clinic, 01 Mar. 2020.

The symptoms of coccidioidomycosis can vary depending on the severity of the infection and the individual's immune response. Some people may experience mild symptoms, such as fever, cough, and fatigue, while others may develop more severe symptoms, including pneumonia, meningitis, and bone or skin infections. Skin lesions and rashes are also common.

Diagnosis of coccidioidomycosis typically involves a combination of physical examination, laboratory tests, and imaging studies. Treatment may involve antifungal medications and supportive care to manage symptoms. In severe cases, hospitalization may be necessary.

Prevention is key in avoiding coccidioidomycosis, which includes avoiding areas with high concentrations of the fungus, using respiratory protection when working in areas where the fungus is present, and taking antifungal medications prophylactically for those who are at high risk.

Prognosis for coccidioidomycosis is generally good for those with mild infections, but can be poor for those with severe infections or underlying conditions such as HIV/AIDS or cancer. Long-term effects of the infection can include lung scarring and joint damage.

The fungi enter the body through traumatic inoculation or inhalation of spores, and may cause a chronic inflammatory response that leads to the formation of granulomas. The hallmark of chromoblastomycosis is the presence of histopathologically distinctive yeast-like structures called "chromoblasts" within the granulomas. These chromoblasts are typically blue-green or bluish-black in color due to the accumulation of melanin.

The clinical presentation of chromoblastomycosis can vary depending on the location and extent of the infection, but may include skin lesions, lymphadenopathy, fever, fatigue, and weight loss. Diagnosis is based on a combination of clinical findings, radiographic imaging (e.g., chest X-ray or CT scan), and histopathologic examination of tissue samples. Treatment typically involves surgical excision of affected tissues, antifungal therapy, and management of associated complications such as inflammation and fibrosis.

Here are 10 key points to remember about histoplasmosis:

1) Histoplasmosis is a fungal disease caused by Histoplasma capsulatum.
2) It primarily affects the lungs and can disseminate to other organs.
3) Inhalation of spores from contaminated soil or bird droppings leads to infection.
4) Symptoms range from mild to severe, including fever, cough, chest pain, fatigue, and difficulty breathing.
5) Diagnosis is based on clinical findings, laboratory tests, and imaging studies.
6) Treatment is primarily supportive, with antifungal medications for severe cases.
7) Prevention includes avoiding exposure to contaminated environments and wearing protective clothing during cleanup or construction activities.
8) Histoplasmosis has a global distribution and is found in many parts of the United States.
9) It is an important occupational hazard for workers involved in construction, mining, and agriculture.
10) In severe cases, histoplasmosis can lead to chronic lung disease, heart problems, and meningitis.

The fungus is found in soil and water and is typically contracted through the inhalation of contaminated dust or the ingestion of contaminated food or water. The symptoms of blastomycosis can vary depending on the severity of the infection, but may include:

* Fever
* Cough
* Shortness of breath
* Skin lesions
* Joint pain
* Swollen lymph nodes

In severe cases, blastomycosis can lead to life-threatening complications such as respiratory failure, cardiovascular problems, and meningitis.

Diagnosis of blastomycosis is based on a combination of clinical findings, laboratory tests, and imaging studies. Treatment typically involves antifungal medications, which can be effective in resolving symptoms and preventing complications. However, the disease can be challenging to diagnose and treat, and long-term follow-up is often necessary to ensure that the infection has been fully cleared.

Preventive measures for blastomycosis include avoiding contact with contaminated soil and water, wearing protective clothing and equipment when working outdoors in areas where the fungus is prevalent, and taking antifungal medications as prescribed by a healthcare provider. Early diagnosis and treatment are critical to preventing severe complications and improving outcomes for patients with blastomycosis.

The disease typically presents with symptoms such as fever, cough, fatigue, weight loss, and night sweats, and can progress to severe respiratory, cutaneous, and disseminated forms if left untreated. The infection is diagnosed through a combination of clinical evaluation, radiological studies, and laboratory tests such as PCR and culture.

Treatment options for paracoccidioidomycosis include antifungal medications such as amphotericin B, fluconazole, and itraconazole, which are often associated with significant side effects and variable efficacy. Surgical debulking may also be considered in certain cases.

The prognosis for paracoccidioidomycosis is generally poor, especially in advanced stages of the disease, with high rates of morbidity and mortality. However, early diagnosis and appropriate treatment can improve outcomes.

If left untreated, sporotrichosis can progress to more serious complications such as bone infections, meningitis, or other life-threatening conditions. Treatment typically involves the use of antifungal medications and surgical debridement of infected tissue.

Sporotrichosis has been associated with a number of risk factors including rural living, outdoor work, and contact with soil or contaminated objects. In some cases, sporotrichosis may also be transmitted through inhalation of fungal spores.

Prevention measures include avoiding activities that involve exposure to soil or other potential sources of the fungus, wearing protective clothing and equipment when working outdoors, and taking precautions such as washing hands regularly to reduce the risk of infection.

The symptoms of aspergillosis depend on the location and severity of the infection. In the lungs, it may cause coughing, fever, chest pain, and difficulty breathing. In the sinuses, it can cause headaches, facial pain, and nasal congestion. In the brain, it can cause seizures, confusion, and weakness.

Aspergillosis is typically diagnosed through a combination of imaging tests such as chest X-rays, CT scans, and MRI scans, along with a biopsy to confirm the presence of Aspergillus fungi.

Treatment of aspergillosis depends on the severity and location of the infection. In mild cases, treatment may involve antifungal medications and supportive care such as oxygen therapy and pain management. In severe cases, treatment may require hospitalization and intravenous antifungal medications.

Preventive measures for aspergillosis include avoiding exposure to dusty or damp environments, managing chronic conditions such as asthma and COPD, and taking antifungal medications as prescribed.

Aspergillosis can be a serious condition, especially in people with weakened immune systems, such as those with cancer, HIV/AIDS, or taking immunosuppressive drugs. In severe cases, aspergillosis can lead to life-threatening complications such as respiratory failure, sepsis, and organ damage.

In conclusion, aspergillosis is a common fungal infection that can affect various parts of the body, and it can be serious and potentially life-threatening, especially in people with weakened immune systems. Early diagnosis and appropriate treatment are essential to prevent complications and improve outcomes.

1. Zygomycosis is a rare and opportunistic fungal infection caused by members of the order Ophiostomatales, which primarily affects the skin and subcutaneous tissues, but can also disseminate to other organs and cause severe systemic disease.
2. Zygomycosis is a type of deep mycosis that is characterized by the presence of broad, flat pseudohyphae and/or thick-walled spherules in the infected tissue, typically seen on histopathological examination.
3. Zygomycosis is an invasive fungal infection that can affect various parts of the body, including the skin, soft tissues, bones, and organs, and is often associated with underlying conditions such as diabetes, immunodeficiency, or malignancy.
4. Zygomycosis is a rare and aggressive fungal infection that can cause significant morbidity and mortality if left untreated, and early diagnosis and treatment are essential to prevent progression of the disease.

Types of candidiasis:

1. Vulvovaginal candidiasis (VVC): a common infection that affects the vagina and vulva; symptoms include itching, burning, and abnormal discharge.
2. Oral thrush (OT): an infection that affects the mouth, often seen in infants and people with weakened immune systems; symptoms include white patches on the tongue and inside the cheeks.
3. Invasive candidiasis (IC): a severe infection that can spread throughout the body, often seen in people with weakened immune systems, such as those with HIV/AIDS or undergoing chemotherapy; symptoms include fever, chills, and difficulty breathing.
4. Candidal balanitis: an infection of the foreskin and glans of the penis; symptoms include redness, swelling, and pain.
5. Diaper rash: a common skin infection that affects infants who wear diapers; symptoms include redness, swelling, and irritability.

Causes and risk factors:

1. Overgrowth of Candida fungus due to an imbalance of the normal flora.
2. Use of antibiotics or steroids that can disrupt the balance of the body's natural flora.
3. Weakened immune system, such as in people with HIV/AIDS or undergoing chemotherapy.
4. Poor hygiene and sanitation.
5. Diabetes mellitus.
6. Pregnancy.
7. Obesity.

Diagnosis:

1. Physical examination and medical history.
2. Microscopic examination of a scraping or biopsy specimen.
3. Cultures of skin, blood, or other body fluids.
4. Polymerase chain reaction (PCR) or other molecular diagnostic techniques to detect the presence of the fungus.

Treatment:

1. Topical antifungal medications, such as clotrimazole, miconazole, or terbinafine, applied directly to the affected area.
2. Oral antifungal medications, such as fluconazole or itraconazole, for more severe infections or those that do not respond to topical treatment.
3. Antibiotics if there is a secondary bacterial infection.
4. Supportive care, such as pain management and wound care.
5. Proper hygiene and sanitation practices.
6. In severe cases, hospitalization may be necessary for intravenous antifungal medications and close monitoring.

Prevention:

1. Practice good hygiene and sanitation.
2. Avoid sharing personal items, such as towels or clothing.
3. Wash hands before touching the affected area.
4. Keep the affected area clean and dry.
5. Use of antifungal powders or sprays on the affected area.
6. Avoid using harsh soaps or cleansers that can irritate the skin.
7. Wear shoes in public areas to prevent exposure to fungal spores.
8. Avoid sharing bathing or showering facilities with others.
9. Dry thoroughly after bathing or swimming.
10. Use of antifungal medications as a prophylactic measure in high-risk individuals, such as those with weakened immune systems.

It's important to note that the best treatment and prevention strategies will depend on the specific type of fungus causing the infection, as well as the severity and location of the infection. It is essential to consult a healthcare professional for proper diagnosis and treatment.

In IPA, the Aspergillus fungus invades the lungs and can cause inflammation, bleeding, and scarring. Symptoms include fever, cough, chest pain, and difficulty breathing. If left untreated, IPA can lead to respiratory failure and death.

IPA is diagnosed through a combination of imaging tests such as chest X-rays, CT scans, and bronchoscopy, as well as through laboratory tests that detect the presence of Aspergillus antigens or DNA in the body.

Treatment of IPA typically involves antifungal medications, such as voriconazole or caspofungin, which are given intravenously for several weeks. In severe cases, hospitalization and supportive care, such as oxygen therapy and mechanical ventilation, may be necessary.

Prevention of IPA is challenging, but efforts to reduce the risk include avoiding exposure to Aspergillus spores, managing underlying conditions that weaken the immune system, and promptly treating any respiratory infections that occur. Early detection and treatment of IPA can improve outcomes and reduce the risk of complications and death.

A type of meningitis caused by a fungal infection. Fungal meningitis is a serious and potentially life-threatening condition that can occur when fungi enter the bloodstream and spread to the membranes surrounding the brain and spinal cord (meninges).

The most common types of fungi that cause fungal meningitis are Aspergillus, Candida, and Cryptococcus. These fungi can be found in soil, decaying organic matter, and contaminated food. People with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs, are at a higher risk of developing fungal meningitis.

Symptoms of fungal meningitis may include fever, headache, stiff neck, sensitivity to light, and confusion. If left untreated, fungal meningitis can lead to serious complications such as brain damage, hearing loss, and seizures. Treatment typically involves the use of antifungal medications, and in severe cases, surgery may be necessary to remove infected tissue or relieve pressure on the brain.

Preventive measures for fungal meningitis include avoiding exposure to fungal sources, practicing good hygiene, and taking antifungal medications as prescribed by a healthcare professional. Early diagnosis and treatment are critical in preventing serious complications and improving outcomes for patients with fungal meningitis.

Examples of OIs include:

1. Pneumocystis pneumonia (PCP): A type of pneumonia caused by the fungus Pneumocystis jirovecii, which is commonly found in the lungs of individuals with HIV/AIDS.
2. Cryptococcosis: A fungal infection caused by Cryptococcus neoformans, which can affect various parts of the body, including the lungs, central nervous system, and skin.
3. Aspergillosis: A fungal infection caused by Aspergillus fungi, which can affect various parts of the body, including the lungs, sinuses, and brain.
4. Histoplasmosis: A fungal infection caused by Histoplasma capsulatum, which is commonly found in the soil and can cause respiratory and digestive problems.
5. Candidiasis: A fungal infection caused by Candida albicans, which can affect various parts of the body, including the skin, mouth, throat, and vagina.
6. Toxoplasmosis: A parasitic infection caused by Toxoplasma gondii, which can affect various parts of the body, including the brain, eyes, and lymph nodes.
7. Tuberculosis (TB): A bacterial infection caused by Mycobacterium tuberculosis, which primarily affects the lungs but can also affect other parts of the body.
8. Kaposi's sarcoma-associated herpesvirus (KSHV): A viral infection that can cause various types of cancer, including Kaposi's sarcoma, which is more common in individuals with compromised immunity.

The diagnosis and treatment of OIs depend on the specific type of infection and its severity. Treatment may involve antibiotics, antifungals, or other medications, as well as supportive care to manage symptoms and prevent complications. It is important for individuals with HIV/AIDS to receive prompt and appropriate treatment for OIs to help prevent the progression of their disease and improve their quality of life.

The symptoms of cryptococcosis vary depending on the location and severity of the infection. In lung infections, patients may experience fever, cough, chest pain, and difficulty breathing. In CNS infections, patients may experience headaches, confusion, seizures, and loss of coordination. Skin infections can cause skin lesions, and eye infections can cause vision problems.

Cryptococcosis is diagnosed by culturing the fungus from body fluids or tissue samples. Treatment typically involves antifungal medications, such as amphotericin B or fluconazole, which may be given intravenously or orally, depending on the severity and location of the infection. In severe cases, surgery may be required to remove infected tissue or repair damaged organs.

Preventive measures for cryptococcosis include avoiding exposure to fungal spores, practicing good hygiene, and maintaining a healthy immune system. For individuals with HIV/AIDS, antiretroviral therapy can help reduce the risk of developing cryptococcosis.

Overall, while rare, cryptococcosis is a serious opportunistic infection that can affect individuals with compromised immune systems. Early diagnosis and prompt treatment are essential to prevent complications and improve outcomes.

The symptoms of mycetoma can vary depending on the type of pathogen causing the infection, but they typically include:

* Swelling and redness of the affected area
* Pain or tenderness to the touch
* Skin thickening and hardening
* Ulceration and discharge of pus
* Fever and malaise

Mycetoma can be difficult to diagnose, as the symptoms can be similar to those of other skin conditions. However, a biopsy of the affected tissue can help to confirm the diagnosis by revealing the presence of granulomas and the pathogen responsible for the infection.

Treatment of mycetoma typically involves antibiotics or antifungal medications, which can help to clear the infection and reduce symptoms. In severe cases, surgical debridement of the affected tissue may be necessary to remove the infected area.

Prevention of mycetoma is challenging, as it is often caused by environmental factors such as soil and water contamination. However, maintaining good wound care and hygiene practices can help to reduce the risk of infection. Early diagnosis and treatment can also help to prevent the spread of the infection and reduce the risk of complications.

Overall, mycetoma is a chronic and debilitating condition that can have a significant impact on quality of life. While it can be challenging to diagnose and treat, early detection and appropriate management can help to improve outcomes for patients affected by this condition.

The condition can affect anyone, but it is more common in older adults and people with certain underlying health conditions such as diabetes, circulatory problems, and immune deficiency disorders. It can also be a side effect of certain medications or a result of exposure to fungal spores in the environment.

There are several types of onychomycosis, including:

1. Distal lateral subungual onychomycosis: This is the most common type and affects the nails of the big toe and thumb.
2. Proximal subungual onychomycosis: This type affects the nails of the fingertips and toes.
3. White superficial onychomycosis: This type is characterized by a white, patchy appearance on the surface of the nail.
4. Candidal onychomycosis: This type is caused by a yeast infection and is more common in people with diabetes or compromised immune systems.

Onychomycosis can be diagnosed through a physical examination, medical history, and fungal cultures of the nail. Treatment options include topical creams and ointments, oral medications, and laser therapy. The best treatment approach depends on the severity and location of the infection, as well as the individual's overall health status.

Preventative measures for onychomycosis include keeping the nails clean and dry, avoiding sharing personal care items, wearing socks that absorb sweat, and using antifungal sprays or powders. Good hygiene practices and regular check-ups with a healthcare provider can also help prevent and manage onychomycosis.

Examples of AROIs include:

1. Pneumocystis pneumonia (PCP): a type of pneumonia caused by the fungus Pneumocystis jirovecii.
2. Tuberculosis (TB): a bacterial infection that can affect the lungs, brain, or other organs.
3. Toxoplasmosis: an infection caused by the parasite Toxoplasma gondii that can affect the brain, eyes, and other organs.
4. Cryptococcosis: a fungal infection that can affect the lungs, brain, or skin.
5. Histoplasmosis: a fungal infection caused by Histoplasma capsulatum that can affect the lungs, skin, and other organs.
6. Aspergillosis: a fungal infection caused by Aspergillus species that can affect the lungs, sinuses, and other organs.
7. Candidiasis: a fungal infection caused by Candida species that can affect the mouth, throat, vagina, or skin.
8. Kaposi's sarcoma: a type of cancer that is caused by the human herpesvirus 8 (HHV-8) and can affect the skin and lymph nodes.
9. Wasting syndrome: a condition characterized by weight loss, fatigue, and diarrhea.
10. Opportunistic infections that can affect the gastrointestinal tract, such as cryptosporidiosis and isosporiasis.

AROIs are a major cause of morbidity and mortality in individuals with HIV/AIDS, and they can be prevented or treated with antimicrobial therapy, supportive care, and other interventions.

Types of fungal lung diseases include:

1. Aspergillosis: This is an infection caused by the fungus Aspergillus, which is commonly found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with cancer, HIV/AIDS, or taking immunosuppressive drugs.
2. Cryptococcosis: This is an infection caused by the fungus Cryptococcus neoformans, which is found in soil and decaying wood. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.
3. Histoplasmosis: This is an infection caused by the fungus Histoplasma capsulatum, which is found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.
4. Pneumocystis pneumonia (PCP): This is an infection caused by the fungus Pneumocystis jirovecii, which is found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.
5. Sporotrichosis: This is an infection caused by the fungus Sporothrix schenckii, which is found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.

Symptoms of fungal lung diseases can include:

* Cough
* Fever
* Chest pain
* Shortness of breath
* Fatigue

Diagnosis of fungal lung diseases is typically made through a combination of physical examination, medical history, and laboratory tests such as chest X-rays, CT scans, and fungal cultures. Treatment usually involves antifungal medications and may also include supportive care to manage symptoms.

Prevention of fungal lung diseases includes:

1. Avoiding exposure to fungal spores by wearing protective clothing and gear when working with soil or decaying organic matter.
2. Maintaining good indoor air quality by using ventilation systems and reducing humidity.
3. Reducing the risk of infection by avoiding close contact with people who are at high risk of developing fungal lung diseases, such as those with weakened immune systems.
4. Avoiding smoking and other tobacco products, which can increase the risk of developing fungal lung diseases.
5. Managing underlying medical conditions, such as HIV/AIDS or taking immunosuppressive drugs, to reduce the risk of developing fungal lung diseases.

A type of meningitis caused by the fungus Cryptococcus neoformans, which can be found in soil and decaying organic matter. The fungus is more common in areas with warm climates and poor air quality. It can cause a variety of symptoms including fever, headache, stiff neck, nausea, vomiting, and mental confusion.

It is most commonly seen in people who have compromised immune systems (such as those with HIV/AIDS or taking immunosuppressive medications), and the elderly. It can be diagnosed by analyzing a sample of cerebrospinal fluid (CSF) for the presence of the fungus or its antigens, or through imaging studies such as CT or MRI scans. Treatment typically involves antifungal medications and supportive care to manage symptoms.

Symptoms of neutropenia may include recurring infections, fever, fatigue, weight loss, and swollen lymph nodes. The diagnosis is typically made through a blood test that measures the number of neutrophils in the blood.

Treatment options for neutropenia depend on the underlying cause but may include antibiotics, supportive care to manage symptoms, and in severe cases, bone marrow transplantation or granulocyte-colony stimulating factor (G-CSF) therapy to increase neutrophil production.

Hematologic neoplasms refer to abnormal growths or tumors that affect the blood, bone marrow, or lymphatic system. These types of cancer can originate from various cell types, including red blood cells, white blood cells, platelets, and lymphoid cells.

There are several subtypes of hematologic neoplasms, including:

1. Leukemias: Cancers of the blood-forming cells in the bone marrow, which can lead to an overproduction of immature or abnormal white blood cells, red blood cells, or platelets. Examples include acute myeloid leukemia (AML) and chronic lymphocytic leukemia (CLL).
2. Lymphomas: Cancers of the immune system, which can affect the lymph nodes, spleen, liver, or other organs. Examples include Hodgkin lymphoma and non-Hodgkin lymphoma.
3. Multiple myeloma: A cancer of the plasma cells in the bone marrow that can lead to an overproduction of abnormal plasma cells.
4. Myeloproliferative neoplasms: Cancers that affect the blood-forming cells in the bone marrow, leading to an overproduction of red blood cells, white blood cells, or platelets. Examples include polycythemia vera and essential thrombocythemia.
5. Myelodysplastic syndromes: Cancers that affect the blood-forming cells in the bone marrow, leading to an underproduction of normal blood cells.

The diagnosis of hematologic neoplasms typically involves a combination of physical examination, medical history, laboratory tests (such as complete blood counts and bone marrow biopsies), and imaging studies (such as CT scans or PET scans). Treatment options for hematologic neoplasms depend on the specific type of cancer, the severity of the disease, and the overall health of the patient. These may include chemotherapy, radiation therapy, stem cell transplantation, or targeted therapy with drugs that specifically target cancer cells.

... "mycoses"). It was originally published in German, but switched 1988 to English. At that time the title was changed to Mycoses. ... Mycoses: Diagnosis, Therapy and Prophylaxis of Fungal Diseases is a monthly peer-reviewed medical journal covering mycology. It ... "Mycoses". 2018 InCites Journal Citation Reports. Web of Science (Science ed.). Clarivate. 2018. Official website v t e ( ...
... "leukemic mycosis fungoides", "Sézary syndrome preceded by mycosis fungoides", or "secondary mycosis fungoides".[needs copy edit ... Mycosis fungoides was first described in 1806 by French dermatologist Jean-Louis-Marc Alibert. The name mycosis fungoides is ... Could it be mycosis fungoides?': an approach to diagnosing patch stage mycosis fungoides". Journal of Hematopathology. 8 (4): ... Mycosis fungoides is the most common type of cutaneous T-cell lymphoma (CTCL), but there are many other types of CTCL that have ...
... is a cutaneous condition that usually presents as solitary or ...
Mycoses. 45 (9-10): 373-7. doi:10.1046/j.1439-0507.2002.00779.x. PMID 12421284. S2CID 4842988. Gorbushina, A.A.; Kotlova, E.R ...
Mycoses. 57 (8): 507-512. doi:10.1111/myc.12189. PMID 24635009. Kane, Julius; Summerbell, Richard; Sigler, Lynne; Krajden, ...
Yablochnik's postgraduate study in the laboratory of mycology and antibiotics at VIEV led to her work on mycoses (diseases of ... In 1978, she led development of a new laboratory for the control and standardization of preparations against mycoses and she ... Rybnikář, A; Chumela, J; Vrzal, V; Krupka, V (1991). "Immunity in cattle vaccinated against ringworm". Mycoses. 34 (9-10): 433- ... Mycoses. 57 (7): 400-405. doi:10.1111/myc.12174. PMID 24621382. S2CID 25324021.{{cite journal}}: CS1 maint: multiple names: ...
Mycoses. 55 (2): 105-109. doi:10.1111/j.1439-0507.2011.02054.x. Bussamara, Roberta; Fuentefria, Alexandre Meneghello; Oliveira ...
Cano J. Guarro J, Figueras M. (March 1991). "Study of the invasion of human hair in vitro by Aphanoascus spp." Mycoses. 34(3): ... Cano J, Guarro J, Mayayo J. (January 1990). "Experimental Pathogenicity of Aphanoascus spp.". Mycoses 33(1): 41-45. de Vries G ...
Mycoses. Blackwell Publishing. 48 (6): 365-377. doi:10.1111/j.1439-0507.2005.01165.x. PMID 16262871. S2CID 1356254. • Lyte M, ...
pannorum". Mycoses. 46 (9-10): 430-432. doi:10.1046/j.1439-0507.2003.00897.x. PMID 14622395. Christen-Zaech, S; Patel, S; ...
Jand SK, Gupta MP (1989). "Dermatomycosis in dogs". Mycoses. 32 (2): 104-5. doi:10.1111/j.1439-0507.1989.tb02213.x. PMID ...
Mycoses. 51 (3): 266-9. doi:10.1111/j.1439-0507.2007.01477.x. PMID 18399908. S2CID 35688902. Yooseph S, Sutton G, Rusch DB, ...
Mycoses. 38 (3-4): 163-166. doi:10.1111/j.1439-0507.1995.tb00042.x. ISSN 0933-7407. "Keratinophyton durum". www.mycobank.org. ...
Mycoses. 50 (2): 121-124. doi:10.1111/j.1439-0507.2006.01332.x. PMID 17305775. S2CID 19565277. Mares D, Tosi B, Poli F, ...
Cutaneous phaeohyphomycosis caused by Cladosporium oxysporum". Mycoses. 42 (1-2): 111-115. doi:10.1046/j.1439-0507.1999.00263.x ...
Mycoses. 42 (4): 339-343. doi:10.1046/j.1439-0507.1999.00457.x. Ali-Shtayeh, M. S. (September 1988). "Keratinophilic fungi ... Mycoses. 35 (3-4): 95-97. doi:10.1111/j.1439-0507.1992.tb00826.x. Singh, I.; Dixit, A. K.; Kushwaha, R. K. S. (January 2010). " ... "Antagonism of Microsporum species by soil fungi". Mycoses. 53 (1): 32-39. doi:10.1111/j.1439-0507.2008.01656.x. PMID 19207833. ...
Mycoses. 50 (1): 58-63. doi:10.1111/j.1439-0507.2006.01310.x. PMID 17302750. S2CID 25493290. Weedon, D. (2002). Skin pathology ... Mycosis-related cutaneous conditions, Animal fungal diseases, Papulosquamous disorders). ...
Mycoses. 57 (4): 247-8. doi:10.1111/myc.12151. PMID 24147779. LA, nagashima (2016). "Immunomodulation over the course of ... Mycoses. 58 (6): 325-36. doi:10.1111/myc.12318. PMID 25808822. (Articles with short description, Short description matches ...
Mycoses. 57 (4): 214-21. doi:10.1111/myc.12145. PMID 24125484. S2CID 24106682. Lang, Charles H.; Pruznak, Anne; Navaratnarajah ...
Mycoses. 54 (2): 179-181. doi:10.1111/j.1439-0507.2009.01776.x. Mahmoud, DA; Hassanein NM; Youssef KA; Abou Zeid MA (July 2011 ...
"Epidemiological trends in skin mycoses worldwide". Mycoses. 51: 2-15. doi:10.1111/j.1439-0507.2008.01606.x. PMID 18783559. ... Beneke, E., Rogers, A. (1996). Medical Mycology and Human Mycoses. California: Star. pp. 85-90. ISBN 0-89863-175-0.{{cite book ... Mycoses. 34 (9-10): 433-436. doi:10.1111/j.1439-0507.1991.tb00809.x. PMID 1820524. S2CID 37335502. Sarkisov, A. K.; Petrovitch ... Mycoses. 54 (6): 870-876. doi:10.1111/j.1439-0507.2011.02015.x. PMID 21615536. S2CID 20736796.{{cite journal}}: CS1 maint: ...
Mycoses and Algal infections". Weedon's Skin Pathology Essentials (2nd ed.). Elsevier. p. 455. ISBN 978-0-7020-6830-0. "ICD-11 ... The dimorphic mycoses". In Spec, Andrej; Escota, Gerome V.; Chrisler, Courtney; Davies, Bethany (eds.). Comprehensive Review of ... Lortholary O, Denning DW, Dupont B (March 1999). "Endemic mycoses: a treatment update". The Journal of Antimicrobial ... Mycoses. 47 (1-2): 62-8. doi:10.1046/j.1439-0507.2003.00953.x. hdl:2027.42/74074. PMID 14998402. S2CID 7319396. Takahashi S, ...
Lee, Soo Chan; Heitman, Joseph (December 2014). "Sex in the Mucoralean Fungi". Mycoses. 57: 18-24. doi:10.1111/myc.12244. PMC ...
Mycoses. 37 (3-4): 71-8. doi:10.1111/j.1439-0507.1994.tb00780.x. PMID 7845423. S2CID 22605873. Figueiredo, Rodrigo Tinoco; ...
Although the mycosis slowly spreads, it usually remains localized to the skin and subcutaneous tissue. Hematogenous and/or ... Chromoblastomycosis is a long-term fungal infection of the skin and subcutaneous tissue (a chronic subcutaneous mycosis). It ... Mycoses. 44 (1-2): 1-7. doi:10.1046/j.1439-0507.2001.00613.x. PMID 11398635. S2CID 9606451. de Andrade TS, Cury AE, de Castro ... Mycosis-related cutaneous conditions, Tropical diseases, Fungal diseases). ...
Vanden Bossche H, Koymans L (1998). "Cytochromes P450 in fungi". Mycoses. 41 Suppl 1: 32-8. doi:10.1111/j.1439-0507.1998. ...
Mycoses. 37 (1-2): 3-10. doi:10.1111/j.1439-0507.1994.tb00277.x. PMID 7935589. S2CID 24703812. Anaissie, E.; Gokaslan, A.; ...
Duggan, J.M.; Wolf, M.D.; Kauffiman, C.A. (May 1995). "Phialophora verrucosa infection in an AIDS patient". Mycoses. 38 (5-6): ... Most strains of P. verrucosa available in culture collections are derived from human mycoses. Phialophora verrucosa is a common ... Mycoses. 48 (6): 456-461. doi:10.1111/j.1439-0507.2005.01150.x. PMID 16262887. S2CID 28365592. Tendolkar, U.M.; Kerkar, P.; ...
Mycoses. 55 Suppl 3: 1-13. doi:10.1111/j.1439-0507.2012.02185.x. PMID 22519657. S2CID 35082539. Gunter, Jen (27 August 2019). ... Mycosis-related cutaneous conditions, Wikipedia medicine articles ready to translate, Vagina, Fungal diseases). ...
Mycoses. 39 (5-6): 211-215. doi:10.1111/j.1439-0507.1996.tb00127.x. PMID 8909032. S2CID 20166266. Saenz-de-Santamaria, M.; ... Mycoses. 49 (2): 91-95. doi:10.1111/j.1439-0507.2006.01195.x. PMID 16466440. S2CID 24588508. Denning, David W; Pashley, ...
Modern Vaccines for Mycoses, replaces PA-96-061, Modern Vaccines for Mycoses and Measles. Investigator-initiated applications ... MODERN VACCINES FOR MYCOSES Release Date: March 6, 1998 PA NUMBER: PA-98-039 P.T. National Institute of Allergy and Infectious ... The goal is to identify and characterize antigens that induce a protective immune response for the major systemic mycoses of ... Relevant projects for the mycoses could address one or more of the following objectives: o The identification of fungal ...
1971)‎. MYCOSES = MYCOSES. Weekly Epidemiological Record = Relevé épidémiologique hebdomadaire, 46 (‎15)‎, 147. https:// ...
Mycosis fungoides is the most common form of a type of blood cancer called cutaneous T-cell lymphoma. Explore symptoms, ... Mycosis fungoides is the most common form of a type of blood cancer called cutaneous T-cell lymphoma. Cutaneous T-cell ... The tumors in mycosis fungoides, which are composed of cancerous T cells, are raised nodules that are thicker and deeper than ... For unknown reasons, mycosis fungoides affects males nearly twice as often as females. In the United States, there are an ...
This article describes common cutaneous mycoses in children: mucocutaneous candidiasis, pityriasis versicolor, tinea corporis, ... Cutaneous mycoses in children B E Elewski. Br J Dermatol. 1996 Jun. ... An update of its use in superficial mycoses. McClellan KJ, Wiseman LR, Markham A. McClellan KJ, et al. Drugs. 1999 Jul;58(1): ... This article describes common cutaneous mycoses in children: mucocutaneous candidiasis, pityriasis versicolor, tinea corporis, ...
The clinical nomenclatures used for the mycoses are based on the (1) site of the infection, (2) route of acquisition of the ... Deep Mycoses. General Concepts. Primary versus opportunistic mycoses. Deep mycoses are caused by primary pathogenic and ... Current magnitude and problems of mycoses. Fungal infections or mycoses cause a wide range of diseases in humans. Mycoses range ... Classification of Mycoses. The clinical nomenclatures used for the mycoses are based on the (1) site of the infection, (2) ...
mycosis: A fungal infection in or on a part of the body. ... Thomson describes a case of mycosis fungoides 16.36 in a young ... Now, it turns out the little rash Brian has under his eye is a mycosis infection, a fungal infection caused by exposure to mold ... Our pediatrician wasnt sure what kind of cream to use to treat mycosis near the eye, so we have an appointment with the ... His hatred made him subject to a physical affliction in the form of a mycosis, a fungus growth which attacked the membranes of ...
... opportunistic mycoses). For many mycoses, ICD-9 codes do not differentiate pulmonary from other types of mycoses. For ICD-10 ... In addition, the ICD-9 classification codes for many mycoses do not differentiate pulmonary from other types of mycoses. ... Decedents with pneumoconiosis and mycosis were rare, and most mycoses were pulmonary: 77% in persons with silicosis; 79% ... with and without ICD-9 code for opportunistic mycoses and ICD-10 codes for unspecified mycoses and opportunistic mycoses. ...
The endemic mycoses blastomycosis, coccidioidomycosis (Valley fever), and histoplasmosis are environmental fungal diseases that ... Calls/Webinars - Algorithms for Diagnosing the Endemic Mycoses Blastomycosis, Coccidioidomycosis, and Histoplasmosis​, Thursday ... Algorithms for Diagnosing the Endemic Mycoses Blastomycosis, Coccidioidomycosis, and Histoplasmosis. *Preparing for the ... Algorithms for Diagnosing the Endemic Mycoses Blastomycosis, Coccidioidomycosis, and Histoplasmosis​, Thursday, September 21, ...
The most common type of CTCL is Mycosis fungoides (MF). ... The most common type of CTCL is Mycosis fungoides (MF). Much ... New systemic treatment options in mycosis fungoides and Sézary syndrome , springermedizin.at Skip to main content Menü Home ... Transformation of mycosis fungoides/Sezary syndrome: clinical characteristics and prognosis. Blood. 1998;92(4):1150-9. CrossRef ... New systemic treatment options in mycosis fungoides and Sézary syndrome verfasst von. Magdalena Seidl-Philipp, MD Van Anh ...
Prot #CBI_2022_MF_DevVal_001: Development and Validation of an Ancillary Diagnostic Test for Mycosis Fungoides (SIGNAL-MF). * ...
Start Over You searched for: Subjects Mycoses -- microbiology ✖Remove constraint Subjects: Mycoses -- microbiology ...
Dallas J. Smith, PharmD1,2; Samantha L. Williams, MPH2; Endemic Mycoses State Partners Group; Kaitlin M. Benedict, MPH2; ... Endemic Mycoses State Partners Group. Guillermo Adame, Arizona Department of Health Services; Laura Rothfeldt, Arkansas ... Suggested citation for this article: Smith DJ, Williams SL, Endemic Mycoses State Partners Group, Benedict KM, Jackson BR, Toda ... AI/AN persons are more commonly affected by endemic mycoses, with blastomycosis incidence approximately six times as high and ...
Phaeohyphomycosis is a term to describe cutaneous and systemic or disseminated mycoses caused by a variety of dematiaceous ... A Rare Case Report of Subcutaneous Mycoses by Rhytidhysteron Rufulum. Author(s):Yadav Sarita, Agarwal Ruchi, Chander Jagdish ... Phaeohyphomycosis is a term to describe cutaneous and systemic or disseminated mycoses caused by a variety of dematiaceous ...
Computer fileLanguage: engger Publication details: Berlin : Grosse Verlag. ISSN: 1439-0507Subject(s): Mycoses -- periodicals ... Mycoses [electronic resource] Contributor(s): Deutschsprachige Mykologische GesellschaftMaterial type: ...
"Re-drawing the Maps for Endemic Mycoses" 185, no. 5 (2020). Ashraf, Nida et al. "Re-drawing the Maps for Endemic Mycoses" vol. ... This review will focus on the evidence underlying the established areas of endemicity for these mycoses as well as new data and ... Blastomycosis Coccidioidomycosis Emergomyces Endemic Diseases Endemic Fungi Fungi Histoplasmosis Humans Mycoses ... Title : Re-drawing the Maps for Endemic Mycoses Personal Author(s) : Ashraf, Nida;Kubat, Ryan C.;Poplin, Victoria;Adenis, ...
Mycoses Assunto da revista: Microbiologia Ano de publicação: 2023 Tipo de documento: Artigo País de afiliação: Nigéria ... Mycoses Assunto da revista: Microbiologia Ano de publicação: 2023 Tipo de documento: Artigo País de afiliação: Nigéria ...
Somatic rearrangement of the TP63 gene preceding development of mycosis fungoides with aggressive clinical course. In: Blood ... Somatic rearrangement of the TP63 gene preceding development of mycosis fungoides with aggressive clinical course. Blood cancer ... Somatic rearrangement of the TP63 gene preceding development of mycosis fungoides with aggressive clinical course. / Chavan, R ... title = "Somatic rearrangement of the TP63 gene preceding development of mycosis fungoides with aggressive clinical course", ...
Fungi causing opportunistic mycoses (Aspergillus spp, black fungus). Multiple Choice Questions. 1)Which of the following are ... Name the possible mycosis reported during the second wave of COVID-19 in India ... d) The major cause of systemic mycoses. 10) Aflatoxin is usually present in moldy foods such as nuts and corn which can be ... 17) In recent years, opportunistic mycoses in immunocompromised individuals is caused by various types of fungi including molds ...
Mycosis fungoides. Mycosis fungoides is the most common type of cutaneous T-cell lymphoma (44%), which has led some authors to ... Mycosis fungoides. Mycosis fungoides is a malignant lymphoma characterized by the expansion of a clone of CD4+ (or helper) ... Folliculotropic mycosis fungoides. The prognosis associated with folliculotropic mycosis fungoides is worse than that for ... Mycosis fungoides variants and subtypes (eg, folliculotropic mycosis fungoides, pagetoid reticulosis, granulomatous slack skin ...
Persons with silicosis were more likely to die with pulmonary mycosis than were those without pneumoconiosis or those with more ... 2010). Concurrent Silicosis and Pulmonary Mycosis at Death. 16(2). Iossifova, Yulia et al. "Concurrent Silicosis and Pulmonary ... Mycosis at Death" 16, no. 2 (2010). Iossifova, Yulia et al. "Concurrent Silicosis and Pulmonary Mycosis at Death" vol. 16, no. ... Title : Concurrent Silicosis and Pulmonary Mycosis at Death Personal Author(s) : Iossifova, Yulia;Bailey, Rachel;Wood, John; ...
Share info and advice with people concerned by Recurrent mycosis ✓ The leading social network for patients, their family and ...
EVA INTIMA® MYCOSIS CLEANSING FLUID is a cleansing liquid specially designed to clean the external genitalia during fungal ... MYCOSIS FOAMING WASH. Antipruritic cleansing foam for external use for cases of fungal infection.. ... Before applying any other product topically, thoroughly clean the area with EVA INDIMA® MYCOSIS CLEANSING FLUID. Apply the ... DISORDERS MYCOSIS CLEANSING FLUID Antipruritic cleaning fluid ... MYCOSIS OVULES. Vaginal suppositories to inhibit the action of ...
Mycosis fungoides: The recommended dosage is 25 to 75 mg orally once weekly as monotherapy; 10 mg/m2 orally twice weekly as ... Mycosis Fungoides The recommended dosage of methotrexate tablets is 25 to 75 mg orally once weekly when administered as a ... Treatment of adults with mycosis fungoides (1.1) •. Treatment of adults with relapsed or refractory non-Hodgkin lymphoma as ... to treat adults with mycosis fungoides (cutaneous T-cell lymphoma) •. in combination with other therapies to treat adults with ...
Mycosis fungoides: The recommended dosage is 25 to 75 mg orally once weekly as monotherapy; 10 mg/m2 orally twice weekly as ... Mycosis Fungoides The recommended dosage of methotrexate tablets is 25 to 75 mg orally once weekly when administered as a ... Treatment of adults with mycosis fungoides (1.1) •. Treatment of adults with relapsed or refractory non-Hodgkin lymphoma as ... to treat adults with mycosis fungoides (cutaneous T-cell lymphoma) •. in combination with other therapies to treat adults with ...
From these results, it may be concluded that FLCZ is a very useful medication in the treatment of deep mycosis in pediatric ... From these results, it may be concluded that FLCZ is a very useful medication in the treatment of deep mycosis in pediatric ... From these results, it may be concluded that FLCZ is a very useful medication in the treatment of deep mycosis in pediatric ... From these results, it may be concluded that FLCZ is a very useful medication in the treatment of deep mycosis in pediatric ...
Biopsy-confirmed mycosis fungoides (MF); clinical stage IB; IIA; IIB; or IIIB. - Patients must have failed or have been ... Low-dose (12 Gy) TSEBT+Vorinostat Versus Low-dose TSEBT Monotherapy in Mycosis Fungoides. Not Recruiting ... low-dose TSEBT alone in participants with mycosis fungoides (MF) Treatment in this study is TSEBT +/- vorinostat, with ... Combined With Vorinostat Versus Low-dose TSEBT Monotherapy in Mycosis Fungoides (MF) ...
A randomized controlled trial evaluating the efficacy and safety of a MYCOFUNGI CREAM in patients with skin mycoses. Roger ...
  • Mycosis fungoides is the most common form of a type of blood cancer called cutaneous T-cell lymphoma. (medlineplus.gov)
  • Mycosis fungoides usually occurs in adults over age 50, although affected children have been identified. (medlineplus.gov)
  • Mycosis fungoides may progress slowly through several stages, although not all people with the condition progress through all stages. (medlineplus.gov)
  • In some affected individuals, patches progress to plaques, the next stage of mycosis fungoides. (medlineplus.gov)
  • The tumors in mycosis fungoides, which are composed of cancerous T cells, are raised nodules that are thicker and deeper than plaques. (medlineplus.gov)
  • Mycosis fungoides was so named because the tumors can resemble mushrooms, a type of fungus. (medlineplus.gov)
  • Spread to other organs can occur in any stage of mycosis fungoides but is most common in the tumor stage. (medlineplus.gov)
  • Mycosis fungoides occurs in about 1 in 100,000 to 350,000 individuals. (medlineplus.gov)
  • For unknown reasons, mycosis fungoides affects males nearly twice as often as females. (medlineplus.gov)
  • The cause of mycosis fungoides is unknown. (medlineplus.gov)
  • It is unclear whether these genetic changes play a role in mycosis fungoides, although the tendency to acquire chromosome abnormalities (chromosomal instability) is a feature of many cancers. (medlineplus.gov)
  • are associated with mycosis fungoides. (medlineplus.gov)
  • Certain variations of HLA genes may affect the risk of developing mycosis fungoides or may impact progression of the disorder. (medlineplus.gov)
  • It is possible that other factors, such as environmental exposure or certain bacterial or viral infections, are involved in the development of mycosis fungoides. (medlineplus.gov)
  • The inheritance pattern of mycosis fungoides has not been determined. (medlineplus.gov)
  • Thomson describes a case of mycosis fungoides 16.36 in a young girl of the age of fourteen, whom he saw in Brussels toward the end of October, 1893. (wordnik.com)
  • Morris 16.37 described an interesting case of universal dermatitis, probably a rare variety of mycosis fungoides (Plate 12). (wordnik.com)
  • Morris thought this case corresponded more to mycosis fungoides than any other malady. (wordnik.com)
  • The most common type of CTCL is Mycosis fungoides (MF). (springermedizin.at)
  • The purpose of this study is to determine if vorinostat combined with low-dose total skin electron beam therapy (TSEBT) offers superior clinical benefit (efficacy & safety) over low-dose TSEBT alone in participants with mycosis fungoides (MF) Treatment in this study is TSEBT +/- vorinostat, with participants stratified by MF stage. (stanford.edu)
  • The two most common types are mycosis fungoides and Sézary syndrome. (medscape.com)
  • In most cases of mycosis fungoides, the diagnosis is reached owing to its clinical features, disease history, and histomorphologic and cytomorphologic findings. (medscape.com)
  • Mycosis Fungoides is a kind of lymphoma. (medicalpicturesinfo.com)
  • Most of the people who are diagnosed with Mycosis Fungoides have to live with the disease the entire life as there is no cure for this. (medicalpicturesinfo.com)
  • This article describes common cutaneous mycoses in children: mucocutaneous candidiasis, pityriasis versicolor, tinea corporis, tinea pedis, onychomycosis and tinea capitis. (nih.gov)
  • Mycoses are classified as superficial, cutaneous, subcutaneous, or systemic (deep) infections depending on the type and degree of tissue involvement and the host response to the pathogen. (nih.gov)
  • Principal tissue sites of deep mycoses in comparison to those of the superficial, cutaneous, and subcutaneous mycoses. (nih.gov)
  • Phaeohyphomycosis is a term to describe cutaneous and systemic or disseminated mycoses caused by a variety of dematiaceous fungi. (ijmrhs.com)
  • Relevant projects for the mycoses could address one or more of the following objectives: o The identification of fungal antigens that generate a protective immune response. (nih.gov)
  • Now, it turns out the little rash Brian has under his eye is a mycosis infection, a fungal infection caused by exposure to mold. (wordnik.com)
  • Fungal infections or mycoses cause a wide range of diseases in humans. (nih.gov)
  • EVA INTIMA® MYCOSIS CLEANSING FLUID is a cleansing liquid specially designed to clean the external genitalia during fungal infections. (eva-intima.com)
  • Interpretation In the state of S~ao Paulo, HTLV-1 and HTLV-2 seem to circulate in male patients with systemic mycoses, and since HTLV-1 could impact fungal disease severity, the identification of co-infection is important regardless of prevalence. (bvs.br)
  • Among persons who died with pneumoconiosis, aspergillosis was the most common pulmonary mycosis. (cdc.gov)
  • The Lancet Regional mycoses such as paracoccidioidomycosis (PCM) and histoplasmosis (HP), and aspergillosis (AP). (bvs.br)
  • No specific gross lesions were appreciated at necropsy, while histopathology evidenced a systemic mycosis in several organs, particularly in the lungs. (unicam.it)
  • https://doi.org/10.1016/j. for HTLV-1/-2 antibodies in serum samples sent to the Instituto Adolfo Lutz, S~ao Paulo, Brazil, for systemic mycosis lana.2022.100339 diagnosis. (bvs.br)
  • Subcutaneous mycoses include a range of different infections characterized by infection of the subcutaneous tissues usually at the point of traumatic inoculation. (nih.gov)
  • Portals of entry of pathogenic and opportunistic fungi causing deep mycoses. (nih.gov)
  • and 118/B48.7 (opportunistic mycoses). (cdc.gov)
  • For ICD-10 codes, we limited data to mycoses coded as pulmonary, opportunistic, and some unspecified type of mycoses (e.g. (cdc.gov)
  • We provided results with and without ICD-9 code for opportunistic mycoses and ICD-10 codes for unspecified mycoses and opportunistic mycoses. (cdc.gov)
  • 17) In recent years, opportunistic mycoses in immunocompromised individuals is caused by various types of fungi including molds. (medicalbiochemist.com)
  • For its low protein binding rate of about 10 per cent and long serum half-life of about thirty hours in adults, FLCZ has been proved highly effective and useful in the treatment of deep-seated mycosis in adult patients. (elsevier.com)
  • Neutrophils and monocytes/macrophages are critical for host defense against invasive candidiasis , the most common deep-seated human mycosis and the fourth-leading cause of nosocomial bloodstream infection in the United States. (nih.gov)
  • The clinical nomenclatures used for the mycoses are based on the (1) site of the infection, (2) route of acquisition of the pathogen, and (3) type of virulence exhibited by the fungus. (nih.gov)
  • In the present study, we have investigated the clinical effectiveness and antifungal activities of FLCZ granules, a new dosage form of the drug, and of intravenous form in pediatric patients with deep mycosis. (elsevier.com)
  • Although the clinical picture of respiratory mycoses resembles that of any other infection, the presentation in several cases is atypical and the diagnosis is delayed. (who.int)
  • We report here the general clinical spectrum of respiratory mycoses and some interesting cases seen at our Centre. (who.int)
  • Mycoses range in extent from superficial infections involving the outer layer of the stratum corneum of the skin to disseminated infection involving the brain, heart, lungs, liver, spleen, and kidneys. (nih.gov)
  • Superficial mycoses are limited to the stratum corneum and essentially elicit no inflammation. (nih.gov)
  • treatment of superficial mycoses, and amphotericin B and flucytosine have been used in treating subcutaneous and systemic mycoses. (britannica.com)
  • His hatred made him subject to a physical affliction in the form of a mycosis , a fungus growth which attacked the membranes of his throat. (wordnik.com)
  • From a total of 2,153 parrots examined at post-mortem, four cases were diagnosed with atypical mycosis and were considered for determination of the fungus species by PCR. (unicam.it)
  • That is, things do get a little odd, but more so after meeting Professor Butler, one of Hicks 'ex-lovers: "" Rueben suffers from a unique breed of mycosis - you've perhaps seen the tumors on his arms and legs, and especially along his spinal column? (wordnik.com)
  • Many of the deeply invasive mycoses are difficult to diagnose early and often difficult to treat effectively. (nih.gov)
  • This disease it's apparently analogous to recent bee's colony collapse disorder and white nose syndrome of bats, which is kind of mycosis , too. (wordnik.com)
  • Deep mycoses involve the lungs, abdominal viscera, bones and or central nervous system. (nih.gov)
  • RESEARCH OBJECTIVES Background The purpose of this initiative is to advance the development of new vaccines for prevention or treatment of the major systemic mycoses of man. (nih.gov)
  • From these results, it may be concluded that FLCZ is a very useful medication in the treatment of deep mycosis in pediatric patients. (elsevier.com)
  • IMSEAR at SEARO: The spectrum of respiratory mycoses in a referral hospital in north-western India. (who.int)
  • Jindal SK, Gupta D, Aggarwal AN, Chakrabarti A. The spectrum of respiratory mycoses in a referral hospital in north-western India. (who.int)
  • Persons with silicosis were more likely to die with pulmonary mycosis than were those without pneumoconiosis or those with more common pneumoconioses. (cdc.gov)
  • Health professionals should consider enhanced risk for mycosis for silica-exposed patients. (cdc.gov)
  • The prevalence of HTLV-1/-2 in patients with sys- infected with HTLV-1 and HTLV-2.7 , 8 However, co- temic mycoses in Latin America is unknown. (bvs.br)
  • There has been an increasing recognition of respiratory mycoses in this country in the recent past. (who.int)
  • For many mycoses, ICD-9 codes do not differentiate pulmonary from other types of mycoses. (cdc.gov)
  • The incidence of clinically apparent coccidioidomycosis and histoplasmosis in HIV+ individuals in highly endemic areas, although variable, has been found to be as high as 25 percent for each mycosis. (nih.gov)
  • Help support Wordnik (and make this page ad-free) by adopting the word mycosis . (wordnik.com)
  • There are few data on paediatric use of fluconazole, although it is available in liquid form, has an excellent safety profile and may become important for treating paediatric mycoses. (nih.gov)
  • Our pediatrician wasn't sure what kind of cream to use to treat mycosis near the eye, so we have an appointment with the dermatologist on Thursday. (wordnik.com)
  • To examine risk for mycosis among persons with silicosis, we examined US mortality data for 1979-2004. (cdc.gov)
  • In response to inquiries from silica-exposed workers concerned about diagnoses of coccidioidomycosis or cryptococcal meningitis for their co-workers, we examined whether excess risk for mycosis exists among persons with silicosis. (cdc.gov)
  • We computed prevalence rate ratios and 95% confidence intervals (CIs) to separately compare pulmonary mycosis prevalence at death among persons with silicosis, asbestosis, and CWP with that for persons in the referent group and to compare pulmonary mycosis prevalence at death among persons with silicosis with that for persons in the 2 pneumoconiosis comparison groups. (cdc.gov)
  • Each ratio was computed by dividing the proportion of mycosis deaths in 1 group by the corresponding measure in the comparison group. (cdc.gov)