Alopecia mucinosa (also known as "Follicular mucinosis," "Mucinosis follicularis,",[1] "Pinkus follicular mucinosis,"[1] and "Pinkus follicular mucinosis-benign primary form"[1]) is a skin disorder that generally presents, but not exclusively, as erythematous plaques or flat patches without hair primarily on the scalp and face.[2]:649[3]:188 This can also present on the body as a follicular mucinosis and may represent a systemic disease.[1][4]. ...
Looking for online definition of cutaneous focal mucinosis in the Medical Dictionary? cutaneous focal mucinosis explanation free. What is cutaneous focal mucinosis? Meaning of cutaneous focal mucinosis medical term. What does cutaneous focal mucinosis mean?
Looking for idiopathic mucinosis? Find out information about idiopathic mucinosis. Accumulations of materials containing mucin or mucinous substances in the skin; sometimes accompanied by papule and nodule formation Explanation of idiopathic mucinosis
The treatment goal for CLM is resolution of the papulonodular lesions and to control the underlying SLE disease.. Sun avoidance and protection with the use of broad spectrum sunscreen that covers both UVA and UVB ranges should be discussed with all patients with CLE, including those with CLM. Although the exact role of UV light in the pathogenesis of CLM is not clear, we do know that UV light plays a role in many other CLE conditions and SLE, which may also be present.. Cigarette smokers are found to have more severe CLE disease. Antimalarials may be less effective in those patients that smoke. As a result, all patients with CLE should begin a smoking cessation program.. Topical therapy can be used in combination with systemic therapies. The effectiveness of topical steroids and calcineurin inhibitors in CLM are not known. However, for limited, focal disease, it can be used for 2 months as a trial.Combining topical steroids and calcineurin inhibitors may provide an added benefit. Intralesional ...
Bexarotene is an associate of a subclass of retinoids that selectively activate retinoid X receptors (RXRs). The chemical name is usually 4-[1-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)ethenyl] benzoic acid.[4] Orally, it has been approved for the treatment of refractory cutaneous T-cell lymphomas (CTCL).[5] Bexarotene gel 1% is indicated for the localized treatment of cutaneous lesions in patients with refractory or persistent CTCL (Stage IA and IB) or whove not tolerated other therapies.[4] Bexarotene gel in addition has been found to be effective in mycosis fungoides and lymphomatoid papulosis lesions refractory to oral bexarotene and denileukin diftitox as adjuvant therapy.[6] It was also noted that topical bexarotene yielded significant hair regrowth when used to treat patients with follicular mucinosis or folliculotropic mycosis fungoides, and thus it was theorized that topical bexarotene may also induce hair regrowth in AA.[7] Recently, Talpur and colleagues conducted a ...
Alopecia Mucinosa is a condition caused due to mucin deposition in hair follicles and sebaceous glands, which undergo epithelial reticular degeneration resulting into follicular papules or plaques associated with hair loss. It usually affects the scalp, face, and neck. Alopecia mucinosa was first reported by Dr. Hermann Pinkus in 1957. It is more frequent in males than in females. Alopecia mucinosa is also known as follicular mucinosis.. There are basically three types of alopecia mucinosa; a primary and acute disorder of young persons, a primary and chronic disorder of older persons, and a secondary disorder associated with benign or malignant disease. ...
As cute as they look, Chinese Shar-pei dogs are afflicted with a potentially dangerous skin disorder which causes mild to severe wrinkling and thickening of the skin. Severe wrinkling can lead to bacterial infection in the skin and entropion (the inward folding of eyelids which can cause eyelashes to rub against the cornea). Scientists recently identified the molecule primarily responsible for this skin condition and its cause. The technical term for this type of skin wrinkling is cutaneous mucinosis, where cutaneous refers to the skin and mucinosis refers to deposits of mucin in the skin. Mucin is a clear jelly-like substance and the main component of mucin is hyaluronic acid (yes, the dermal filler). The researchers hypothesised that the accumulation of hyaluronic acid in the dermis caused mucinosis in the Shar-pei. By examining the correlation between mucinosis and the levels of blood hyaluronic acid, the researchers identified that the accumulation of hyaluronic acid was responsible for the ...
If the dog scratches and ruptures the bubbles or vesicles, or this accidentally happens from something like the rubbing of a collar, and the vesicles become inflamed, you should immediately apply a non-corticosteroid anti-inflammatory ointment on the wounds. If dogs are treated with cortisone, they tend to lose their fatty tissue and mucin deposits in the skin folds about the head (eyes, forehead), flews, and carpal ligaments. Besides, cortisone also dehydrates the tissue, and these side effects can lead to further problems. Normally, Shar-Pei dogs with idiopathic mucinosis are not treated, since the symptoms tend to disappear on their own in time ...
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The cutaneous mucinoses are a heterogeneous group of diseases in which mucin accumulates in the skin or within the hair follicle. We divide the cutaneous mucinoses into two groups: the distinctive cutaneous mucinoses in which the mucin deposit is a distinctive histopathologic feature that manifests as a clinically specific lesion, and the diseases associated with histopathologic mucin deposition as an additional finding. This article deals with the clinical and histopathologic features and the treatment of the distinctive cutaneous mucinoses and updates their classification. They may be divided, according to the microscopic location of mucin, into dermal and follicular mucinoses. The former group includes; lichen myxedematosus, acral persistent papular mucinosis, reticular erythematous mucinosis, scleredema, dysthyroidotic mucinoses (i.e. localized myxedema, generalized myxedema, papular mucinoses associated with thyroid diseases), papular and nodular mucinosis associated with lupus ...
TY - JOUR. T1 - A clinicopathologic study of 15 cases of angiolymphoid hyperplasia with eosinophilia. AU - Yoon, Jin Choi. AU - Mi, Ryung Roh. AU - Lee, Min Geol. PY - 2008/7/1. Y1 - 2008/7/1. N2 - Background: Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon distinctive vascular lesion characterized by proliferation of endothelial cells. Because of its rarity, the clinical and pathological aspects of ALHE have not been fully studied in Korea. Objective: The purpose of our investigation was to describe the clinical and pathological characteristics of ALHE. Methods: We reviewed the medical records, clinical photographs and histological slides of 15 patients who were diagnosed as ALHE at Severance hospital. Results: Of the 15 patients, 60% were men and 40% women. The average onset age of men was 53.7 years, women 33.2 years. Overall average onset age was 45.5 years. The scalp was the most frequently involved site in ALHE. Pruritus was the most common symptom. Two of four patients ...
Carmen Boente , M, Primc , NB, Asial , RA, Winik , BC. "Familial cutaneous collagenoma: a clinicopathologic study of two new cases". Pediatr Dermatol. vol. 21. 2004. pp. 33-8. (Case report of a family with familial cutaneous collagenoma and review of the literature of connective tissue nevi.). Shah , KR, Wells , MJ, Stetson , CL. "CD34+ connective tissue nevi: Are they unusual?". J Am Acad Dermatol . vol. 62. 2010. pp. 719-20. (Case report followed by a retrospective analysis of connective tissue nevi of the collagen-type as related to CD34 positivity.). Shah , KN, Anderson , E, Junkins-Hopkins , J, James , WD. "Medallion-like dermal dendrocyte hamartoma". Pediatr Dermatol . vol. 24. 2007. pp. 632-6. (Case report and review of medallion-like dermal dendrocyte hamartoma.). Biesecker , L. "The challenges of Proteus syndrome: diagnosis and management". Eur J Hum Genet . vol. 14. 2006. pp. 1151-7. (Review of Proteus syndrome focusing on diagnosis and management.). Ryder , HF, Antaya , RJ. "Nevus ...
Brandon L. Adler, Aimee E. Krausz, Aurelia Minuti, Jonathan I. Silverberg, Hadar Lev-Tov, Epidemiology and treatment of angiolymphoid hyperplasia with eosinophilia (ALHE): A systematic review, Journal of the American Academy of Dermatology, 2016, 74, 3, ...
Sanati S, Leonard M, Khamapirad T, Eltorky MA. Nodular mucinosis of the breast: a case report with pathologic, ultrasonographic, and clinical findings and review of the literature. Arch Pathol Lab Med. 2005 Mar;129(3):e58-61 ...
Reibeisenhaut - Wikipedia.Reibeisenhaut ist ein umgangssprachlicher Begriff für folgende Krankheitsbilder: Mucinosis follicularis; Keratosis pilaris (Syn.: Karatosis follicularis)--Hidrozytom - Wikipedia.Ein Hidrozytom (engl. hydrocytoma; ICD-O 8404/0) ist eine gutartige Gewebeneubildung aus der Familie der Adenome. Es handelt sich um zystische Papeln des ...--Imiquimod - Wikipedia.Imiquimod ist ein Arzneistoff aus der Gruppe der Virostatika, der zur Behandlung von kleinem, oberflächlichem Basalzell-Hautkrebs , aktinischer Keratose und ...--Johnny Thunders - Wikipedia.Johnny Thunders, eigentlich John Anthony Genzale, Jr, (* 15. Juli 1952 in Queens, New York; † 23. April 1991 in New Orleans, Louisiana), war ein New Yorker Punk ...--Christina Aguilera/Diskografie - Wikipedia.Diese Diskografie ist eine Übersicht über die musikalischen Werke der US-amerikanischen Pop-Sängerin Christina Aguilera. Weltweit hat sie den Quellenangaben ...--Whitney Houston/Diskografie - Wikipedia.Diese Diskografie ...
TY - JOUR. T1 - Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III). AU - Weaver, David. AU - Norby, Audrey R.. AU - Rosenfeld, Jill A.. AU - Proud, Virginia K.. AU - Spangler, Brooke E.. AU - Ming, Jeffrey E.. AU - Chisholm, Elizabeth. AU - Zackai, Elaine H.. AU - Lee, Beom Hee. AU - Edelmann, Lisa. AU - Desnick, Robert J.. PY - 2015/5/1. Y1 - 2015/5/1. N2 - Focal facial dermal dysplasias (FFDD) are characterized by congenital bitemporal or preauricular atrophic skin lesions, and either autosomal dominant or autosomal recessive inheritance. Setleis syndrome (SS), FFDD type III, is a severe form of FFDD with the ectodermal lesions plus other striking facial features. Autosomal recessive nonsense and frameshift mutations in TWIST2 have been found to cause SS in some but not all individuals. Here, we report on four unrelated individuals, one with an unclassified FFDD and the other three with classic SS. Chromosomal microarray analyses ...
In ALHE, an underlying AV shunt is present as a result of damage to and repair of an artery or vein. The lesions may recur if this underlying AV shunt is not excised, that is why treatment with surgical excision is successful in 65% of cases. Mohs micrographic surgery, including excision of the abnormal vessels at the base of the lesion, may be more effective. There tends to be a lot of bleeding during surgery ...
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The Cdc42- and Rac-induced formation of stress fibres was dependent on the activation of Rho small G protein. This suggests that the role of ATL1 on dendritic morphogenesis depends on its GTPase activity. Anaplasma bodies finitely purified by affinity chromatography to eliminate all traces of erythrocytic stromata were not agglutinated by serum from calves having acute anaplasmosis. The patterns of isolates can be grouped by the animal of origin (e.g. Aneurysm of superficial temporal artery in angiolymphoid hyperplasia lesions We present the argument that the majority of low-molecular-weight organic compounds made and secreted by microbes play roles as cell-signalling molecules in the environment. However, such results are usually limited to carbon nanotube/neuron hybrids formed on a monolayer of dissociated brain cells. Concentration of intrinsic factor and vitamin buy cialis B12-binding activities of fractions of desiccated hog stomach. Isolation and characterization of VceC gain-of-function ...
Pachydermoperiostosis is a rare inherited disorder which presents with finger clubbing, facial enlargement, and periostitis. A case is described in which surgery for ptosis was performed and the differential diagnosis of the condition is discussed. The histological and ultrastructural appearances of the eyelids show sebaceous gland hyperplasia and excessive deposition of mucin in the dermis and would suggest that pachydermoperiostosis may be an example of a cutaneous mucinosis. ...
Conducted an immunohistochemical study and observed that the dermal infiltrate in patients with S zary syndrome mainly showed a T-helper 2 (Th2) cytokine profile, in contrast to a T-helper 1 (Th1) cytokine profile in benign reactive erythroderma, which suggests that a relatively uniform clinical picture in erythroderma does not imply similar pathomechanisms for various etiologies. Information on erythrodermic psoriasis a chronic disease of the auto immune system which affects the skin. Guttate psoriasis symptoms can be severe and lead to fatality if left untreated. Erythrodermic psoriasis is one of the rarer forms of psoriasis marked by redness over most of the body and skin shedding. Hospitalization may be required for initial evaluation and treatment since many of these patients are elderly and the skin involvement is extensive leading to significant mortality risk. Psoriasis: Erythrodermic psoriasis is a rare and severe form of psoriasis occurring in 1-2.25 of patients with psoriasis. ...
Erythrodermic psoriasis (EP) is the most severe form of psoriasis. Although it may develop de novo, it is most commonly associated with long-standing, active disease. EP develops acutely or following a subacute or chronic course. The erythrodermic phase is dominated by generalized erythema and scaling that can be accompanied by an inability to maintain homeostatic functions, a potentially life-threatening complication. Management of EP is difficult and medication should be administered not only to treat psoriasis but also to treat the erythrodermic syndrome and extracutaneous complications. The therapies that are available to treat EP include traditional systemic drugs (such as methotrexate, acitretin, and cyclosporine) and the biological agents (such as etanercept, infliximab, adalimumab, and ustekinumab), which can be used as monotherapy or as part of combined therapy. Clinical experience of treating these disorders with biological agents is limited. As there is a lack of high-quality ...
Cytotoxic Shock Prostration of bodily functions caused by high levels of cytotoxins. It can be treated with inaprovaline.. Darnays Disease A deadly ailment that attacks the brain and nervous system of its victim.. Dermal Dysplasia Skin disorder caused by an overexposure of the skin to dangerous levels of thermal and ultraviolet radiation.. Forrester-Trent Syndrome Degenerative neurological disorder that is very rare and, if left untreated, can cause paralysis and even death.. Hesperan Thumping Cough A flu-like affliction.. Holodiction A psychological condition where an individual gets so caught up in holographic simulations that the real world becomes unimportant. Also known as "Holodeck Addiction.". HTDS Holo-Transference Dementia Syndrome. A medical condition in which someone becomes so disoriented within a holographic simulation that they lose their sense of identity and start to think that they are part of the program.. Irumodic Syndrome Degenerative disorder that causes progressive ...
Slavotinek AM, Mehrotra P, Nazarenko I, Tang PL, Lao R, Cameron D, Li B, Chu C, Chou C, Marqueling AL, Yahyavi M, Cordoro K, Frieden I, Glaser T, Prescott T, Morren MA, Devriendt K, Kwok PY, Petkovich M, Desnick RJ. Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. Hum Mol Genet. 2013 Feb 15; 22(4):696-703. View in: PubMed ...
Lupus tumidus is a rare immunological disorder whose pathogenesis is not fully understood. Although on the one hand there are some differences in (1) the clinical morphology of lesions, (2) the histopathology picture, as well as in (3) serological profile of lupus tumidus patients at the current moment, the disease is regarded as a subform of chronic cutaneous lupus erythematosus. Differential diagnosis requires the exclusion of many diseases such as Jessner Kanoff lymphocytic infiltration, polymorphous light eruption, and reticular erythematous mucinosis. Differentiation between them is not always easy. The standard treatment regimen of patients with lupus tumidus is based on local and systemic application of corticosteroids, azathioprin, dapsone, mepacrine, chloroquine, and hydroxychloroquine. Modern treatment options include the use of pulsed dye laser, tacrolimus 0.1 % ointment and photophoresis. We present a 42-year-old patient with unilateral atypical form of lupus tumidus who was ...
Pain management information for pain medicine healthcare professionals in treating and caring for their patients. Clinical Pain Advisor offers news, case studies and more.
Products and treatments for Skin Psoriasis such as Plaque, Erythrodermic, Gutate, Pustular etc. Psorcure Treatment Plan for clear and clean skin from psoriasis
Department of Dermatology, Cumberland Infirmary, Carlisle CA2 7HY, U.K.*Department of Dermatology, Raigmore Hospital, Inverness IV2 3UJ, U.K. ...
Mycosis Fungoides is a rare type of skin lymphoma (tumors of the blood). This site will describe about mycosis fungoides, causes of mycosis fungoides and treatment, possible symptoms and its related complications includes itching, tumors and patches.
Do You Have Mycosis Fungoides, Familial? Join friendly people sharing true stories in the I Have Mycosis Fungoides, Familial group. Find support forums, advice and chat with groups who share this life experience. A Mycosis Fungoides, Familial anonymo...
First, lets define what mycosis fungoides is. It is a type of blood cancer. What it does is it affects the skin of the person primarily, and then over time, it will slowly progress internally. Common symptoms include but not limited to itchy skin, skin lesions, tumors, and rash.. The cause of this type of cancer until now is still unclear. Most of the case, it is not hereditary also it usually affects people who are at the age of 20 and more. Men are the ones who get this more compared to women. Various treatments include ultraviolet light, exposure to the sunlight, chemotherapy, topical corticosteroids, as well as radiotherapy.. Lets discuss in detail about its symptoms that are visible. One thing is for sure; it does affect the skin. So, there will be lesions, rashes, tumors, and even itching is also common. The symptoms do not appear right away. They do pop up progressively. Thus, expect during the early stages of mycosis fungoides, there will be the appearance of lesions of which will be ...
Mycosis fungoides associated with unusual epidermal hyperplasia.: A 58-year-old white woman presented with widespread pruritic brownish plaques and hyperpigment
Psoriasis is a common inflammatory disease of the skin marked by excessive scaling associated with inflammation, affecting about 2 % of the word population (1). The severity of psoriasis runs from relatively minor disease consisting of 1 or 2 small plaques to erythrodermic
Cardiology news, research and treatment articles offering cardiology healthcare professionals cardiology information and resources to keep them informed.
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BIOSKIN EVOLUTION® allows us to be able to convey this wavelength exclusively on the vitiligo spot and in depth towards the perifollicular melanocytes without causing the damages due to all the other solar radiation of which mainly infrared and ultraviolet rays A.. ...
Sézary syndrome (SS) and Mycosis Fungoides (MF) are T-cell lymphomas whose primary manifestation is in the skin. Mycosis Fungoides, is the most common form of cutaneous T-cell lymphoma. It generally affects the skin, but may progress internally over time.The name mycosis fungoides is somewhat misleading--it loosely means "mushroom-like fungal disease". The disease, however, is not fungal infection but rather a type of non-Hodgkins lymphoma. It was so named because the skin tumors of a severe case as having a mushroom-like appearance.. Sézarys disease (or "Sézary syndrome") is a type of cutaneous lymphoma characterized by Albert Sézary."Sézarys cells" are T-cells that have pathological quantities of mucopolysaccharides. Sézarys disease is sometimes considered a late stage of mycosis fungoides. Click here for instructions on how to download the free FCS Express Reader to view and manipulate the sample cases.. ...
None! Mycosis fungoides is the common name for the most common type of cutaneous T-cell lymphoma. A lymphoma is a malignancy of the white blood cells that are known as lymphocytes. Mycosis fungoides primary involves the skin and produces patches, plaques and tumors. The patches may be scaly or flaky and can thus look a lot like an ordinary rash such as the rash of proriasis or of a non-specific dermatitis. Many times, the plaque-like rash will look like a fungal dermatitis, and thus the name for the syndrome. However, there really is not a fungus involved.. ...
The first choice in natural skin care and fine body care products, this butter forms a breathable, water-resistant film and is the leading natural product for moisturizing; Shea Butter is a superior moisturizer. This treatment is pouring warm oil on the forehead without interruption for 25 minutes. Even though palmar-plantar psoriasis can affect less than 5 percent of body surface area in some cases, the disability and severity of the disease the patient experiences may warrant a is psoriasis itchy zits aggressive therapy. Please be aware that email is not a secure means of communication and spam filters may prevent your email from reaching the health professional. Nails may become pitted or infected-looking, or even lift from the nail bed entirely.
TY - JOUR. T1 - Mycosis fungoides with testicular involvement. T2 - A rare phenomenon. AU - Khawaja, Muhammad Rizwan. AU - Mark, Lawrence. AU - Alexander, Riley E.. AU - Nassiri, Mehdi. AU - Azar, Jose. PY - 2012/7. Y1 - 2012/7. UR - http://www.scopus.com/inward/record.url?scp=84862316848&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=84862316848&partnerID=8YFLogxK. U2 - 10.1016/j.leukres.2012.03.009. DO - 10.1016/j.leukres.2012.03.009. M3 - Article. C2 - 22560335. AN - SCOPUS:84862316848. VL - 36. JO - Leukemia Research. JF - Leukemia Research. SN - 0145-2126. IS - 7. ER - ...
TY - JOUR. T1 - Mycosis fungoides and Sézary syndrome. T2 - Clinical, immunological and molecular distinctions that suggest two different diseases. AU - Wu, Xuesong. AU - Hwang, Samuel T. PY - 2012/4. Y1 - 2012/4. N2 - Although mycosis fungoides and Sézary syndrome are presently defined by the WHO/European Organization for Research and Treatment of Cancer criteria as two distinct subtypes of cutaneous T-cell lymphoma, the two diseases present with some overlapping clinical and pathological features and share the same staging system. Advances in understanding the roles and immunologic features of different subsets of T helper cells have allowed researchers to segregate mycosis fungoides and Sézary syndrome with more precision, suggesting that these diseases, despite some similarities, arise from distinct T-cell subsets. New evidence acquired from recent studies in genetics and molecular signaling pathways has contributed to a more comprehensive understanding of these two disease entities, ...
AbstractTHIRTEEN patients with mycosis fungoides have been seen at the Cleveland Clinic. Nine were men and 4 women. The youngest patient to develop the disease in this series was a 22-year-old woman and the oldest a woman aged 71.Twelve of the patients were white and 1 was colored. Occupation was not significant. The duration of the disease before being seen at the Clinic varied from 1 month to 10 years.One patient developed dermatitis venenata which was followed by a generalized exfoliative dermatitis on which lesions of mycosis fungoides developed 4 years later. Another patient had
Mycosis fungoides and Sézary syndrome are diseases in which lymphocytes (a type of white blood cell) become malignant (cancerous) and affect the skin.
I HAVE JUST BEEN INFORMED THAT I HAVE THE ABOVE DISEASE AND WOULD BE INTERESTED IN ANY INFO ON IT AND IN PARTICULAR ANY CLINICAL RESULTS FROM INTEFERON TREATMENT AND LONG TERM IMPLICATIONS. THANK YOU, EDWIN H HALL JR 173 WASHINGTON VAALLEY ROAD MORRISTOWN , NEW JERSEY 07960 ...
Alopecia areata (al-uh-PEE-shuh air-ee-AH-tuh) is a condition that causes baldness on the scalp and sometimes elsewhere on the body. Another area of fascination concerns the modification of perifollicular nerves. The reality that patients with peladera areata occasionally report itching or pain on influenced areas raises the possibility of modifications in the peripheral stressed system. Circulating…