Benign DERMATOSIS caused by a loss of dermal ELASTIC TISSUE resulting in localized sac-like areas of flaccid skin. It can be either primary (idiopathic) or secondary to other skin conditions, PENICILLAMINE use, or premature birth.
An inflammatory, pruritic disease of the skin and mucous membranes, which can be either generalized or localized. It is characterized by distinctive purplish, flat-topped papules having a predilection for the trunk and flexor surfaces. The lesions may be discrete or coalesce to form plaques. Histologically, there is a "saw-tooth" pattern of epidermal hyperplasia and vacuolar alteration of the basal layer of the epidermis along with an intense upper dermal inflammatory infiltrate composed predominantly of T-cells. Etiology is unknown.
Connective tissue comprised chiefly of elastic fibers. Elastic fibers have two components: ELASTIN and MICROFIBRILS.
A human infant born before 37 weeks of GESTATION.
An infant during the first month after birth.
The age of the conceptus, beginning from the time of FERTILIZATION. In clinical obstetrics, the gestational age is often estimated as the time from the last day of the last MENSTRUATION which is about 2 weeks before OVULATION and fertilization.
Synthetic material used for the treatment of burns and other conditions involving large-scale loss of skin. It often consists of an outer (epidermal) layer of silicone and an inner (dermal) layer of collagen and chondroitin 6-sulfate. The dermal layer elicits new growth and vascular invasion and the outer layer is later removed and replaced by a graft.
The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS.
The process of aging due to changes in the structure and elasticity of the skin over time. It may be a part of physiological aging or it may be due to the effects of ultraviolet radiation, usually through exposure to sunlight.
3-Mercapto-D-valine. The most characteristic degradation product of the penicillin antibiotics. It is used as an antirheumatic and as a chelating agent in Wilson's disease.
Fluid accumulation within the PERICARDIUM. Serous effusions are associated with pericardial diseases. Hemopericardium is associated with trauma. Lipid-containing effusion (chylopericardium) results from leakage of THORACIC DUCT. Severe cases can lead to CARDIAC TAMPONADE.
CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION).
It is a form of protection provided by law. In the United States this protection is granted to authors of original works of authorship, including literary, dramatic, musical, artistic, and certain other intellectual works. This protection is available to both published and unpublished works. (from Circular of the United States Copyright Office, 6/30/2008)
Sequential operating programs and data which instruct the functioning of a digital computer.
Tumors or cancer of the SKIN.
The legal authority or formal permission from authorities to carry on certain activities which by law or regulation require such permission. It may be applied to licensure of institutions as well as individuals.
Duties that are based in ETHICS, rather than in law.
Conferences, conventions or formal meetings usually attended by delegates representing a special field of interest.
An inherited disorder due to defective reabsorption of CYSTINE and other BASIC AMINO ACIDS by the PROXIMAL RENAL TUBULES. This form of aminoaciduria is characterized by the abnormally high urinary levels of cystine; LYSINE; ARGININE; and ORNITHINE. Mutations involve the amino acid transport protein gene SLC3A1.
An abnormal elevation of body temperature, usually as a result of a pathologic process.
A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years.
A variable mixture of the mono- and disodium salts of gold thiomalic acid used mainly for its anti-inflammatory action in the treatment of rheumatoid arthritis. It is most effective in active progressive rheumatoid arthritis and of little or no value in the presence of extensive deformities or in the treatment of other forms of arthritis.
Adverse cutaneous reactions caused by ingestion, parenteral use, or local application of a drug. These may assume various morphologic patterns and produce various types of lesions.
A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated.
A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow.
The main artery of the thigh, a continuation of the external iliac artery.
Ultrasonography applying the Doppler effect combined with real-time imaging. The real-time image is created by rapid movement of the ultrasound beam. A powerful advantage of this technique is the ability to estimate the velocity of flow from the Doppler shift frequency.
Autoantibodies directed against various nuclear antigens including DNA, RNA, histones, acidic nuclear proteins, or complexes of these molecular elements. Antinuclear antibodies are found in systemic autoimmune diseases including systemic lupus erythematosus, Sjogren's syndrome, scleroderma, polymyositis, and mixed connective tissue disease.
Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982).
Either of the two principal arteries on both sides of the neck that supply blood to the head and neck; each divides into two branches, the internal carotid artery and the external carotid artery.
A chronic form of cutaneous lupus erythematosus (LUPUS ERYTHEMATOSUS, CUTANEOUS) in which the skin lesions mimic those of the systemic form but in which systemic signs are rare. It is characterized by the presence of discoid skin plaques showing varying degrees of edema, erythema, scaliness, follicular plugging, and skin atrophy. Lesions are surrounded by an elevated erythematous border. The condition typically involves the face and scalp, but widespread dissemination may occur.
Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS.
A desmosomal cadherin that is an autoantigen in the acquired skin disorder PEMPHIGUS VULGARIS.
A desmosomal cadherin that is an autoantigen in the acquired skin disorder PEMPHIGUS FOLIACEUS.
Visible accumulations of fluid within or beneath the epidermis.
Antibodies that react with self-antigens (AUTOANTIGENS) of the organism that produced them.
A subtype of HLA-DRB beta chains that includes over one hundred allele variants. The HLA-DRB1 subtype is associated with several of the HLA-DR SEROLOGICAL SUBTYPES.
A group of desmosomal cadherins with cytoplasmic tails that resemble those of classical CADHERINS.
Clinically atypical nevi (usually exceeding 5 mm in diameter and having variable pigmentation and ill defined borders) with an increased risk for development of non-familial cutaneous malignant melanoma. Biopsies show melanocytic dysplasia. Nevi are clinically and histologically identical to the precursor lesions for melanoma in the B-K mole syndrome. (Stedman, 25th ed)
A nevus containing melanin. The term is usually restricted to nevocytic nevi (round or oval collections of melanin-containing nevus cells occurring at the dermoepidermal junction of the skin or in the dermis proper) or moles, but may be applied to other pigmented nevi.
A circumscribed stable malformation of the skin and occasionally of the oral mucosa, which is not due to external causes and therefore presumed to be of hereditary origin.
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)
A malignant neoplasm derived from cells that are capable of forming melanin, which may occur in the skin of any part of the body, in the eye, or, rarely, in the mucous membranes of the genitalia, anus, oral cavity, or other sites. It occurs mostly in adults and may originate de novo or from a pigmented nevus or malignant lentigo. Melanomas frequently metastasize widely, and the regional lymph nodes, liver, lungs, and brain are likely to be involved. The incidence of malignant skin melanomas is rising rapidly in all parts of the world. (Stedman, 25th ed; from Rook et al., Textbook of Dermatology, 4th ed, p2445)
A macular lesion on the side of the FACE, involving the CONJUNCTIVA and EYELIDS, as well as the adjacent facial skin, SCLERA; OCULOMOTOR MUSCLES; and PERIOSTEUM. Histological features vary from those of a MONGOLIAN SPOT to those of a BLUE NEVUS.

Circumscribed lenticular anetoderma in an HIV-infected man with a history of syphilis and lichen planus. (1/3)

Anetoderma is an uncommon dermatosis that manifests as discrete foci of well-circumscribed, atrophic skin. The condition can be idiopathic or can be secondary to a number of associated cutaneous diseases. Whereas the pathophysiologic mechanisms remain unknown, anetoderma results from diminished elastic fibers in the dermis. We present an unusual case of localized, lenticular anetoderma in a man with HIV, a history of syphilis, and lichen planus. Both of these infections have been associated with anetoderma. Although his lesions are vaguely reminiscent of a variant of syphilitic anetoderma described in the 1930s, they are confined to a smaller anatomic distribution, differ in size, and have a papular appearance. As anetoderma can develop in the context of infectious disease, a diagnosis of anetoderma should trigger a thorough examination and evaluation for treatable concomitant illnesses.  (+info)

Papillary dermal elastosis. (2/3)

There are numerous acquired disorders of elastic tissue that are distinguished by a combination of clinical appearance, location, gender, age of onset, and characteristic histopathologic findings. We present a case of a 36-year-old man with multiple confluent, hypopigmented papules that coalesced into plaques with prominent follicular ostia over the dorsal aspects of the forearms, shoulders, upper chest, and upper back. Histologically there was selective loss of papillary dermal elastic fibers. The clinical and histopathologic findings in this case are consistent with an acquired disorder of elastic tissue which we believe represents the second reported case of papillary dermal elastosis.  (+info)

Anetoderma secondary to antiphospholipid antibodies. (3/3)

Anetoderma is an elastolytic disorder that is associated with a number of infectious and autoimmune disorders. We present a case of a patient with generalized anetoderma, who was later found to have positive antinuclear antibodies and antiphospholipid antibodies (APAs). Numerous other cases have been reported in literature and some authors have suggested that anetoderma is a highly specific sign of APAs, with or without other manifestations of systemic lupus erythematosus or antiphospholipid syndrome [14]. Thus, work up for connective-tissue disorders should be considered in any patients who present with this skin finding.  (+info)

Isolated, small lesions of anetoderma presenting at birth have been reported in twins born at 25 weeks of gestational age. We report the first case of widespread congenital anetoderma occurring in an infant born at 24 weeks of gestation weighing 640
Anetoderma: Benign DERMATOSIS caused by a loss of dermal ELASTIC TISSUE resulting in localized sac-like areas of flaccid skin. It can be either primary (idiopathic) or secondary to other skin conditions, PENICILLAMINE use, or premature birth.
I was recently diagnosed with anetoderma after biopsy. Saw rhematogy for a full workup and was told no underlying condition or cure.
I have this as well , am 20 was diagnosed at 14. I have been to many doctors with no hope of cure. Was recommended to NYC to a lazer treatment office. They used painful refractor lasers basically burning my skin to create new skin in hope for some answers . I did this for 5 months each time treating new skin with new lasers and heats. The biopsies after this time period showed no change in the skin. I know how devastating this disease is but i just want you all to know i have seen the doctors working their asses off to find a cure. I put myself through hell for those months just tryin ...
Humorous views on interesting, bizarre and amusing articles, submitted by a community of millions of news junkies, with regular Photoshop contests.
我々の皮膚は常に外界からの様々な刺激にさらされている.その刺激の代表的なものとして太陽光線中の紫外線があげられる.紫外線は皮膚癌の発生の誘因となる他に,紫外線の曝露により皮膚には光老化と称される変化が生じてくる.光老化の特徴的な変化として皮膚表面のびまん性の色素沈着と深い皺があげられるが,その変化を特徴づけるものとして皮膚真皮におけるsolar elastosisと称される膠原線維・弾性線維の変化がある.この皮膚光老化には紫外線による酸化ストレスが深く関与していると考えられている.一方,酸化ストレスが関与する全身疾患の一つとしてとして全身性強皮症(systemic sclerosis ; ...
The second issue with the shave excision is fat herniation, iatrogenic anetoderma, and hypertrophic scarring. As the deep shave ...
Atrophic DFSP resemble other benign lesions such as morphea, idiopathic atrophoderma, atrophic scar, anetoderma or lipoatrophy ...
... accumulation in actinic damage and absence in anetoderma". Br. J. Dermatol. 137 (1): 51-58. doi:10.1111/j.1365-2133.1997. ...
Anetoderma (anetoderma maculosa, anetoderma maculosa cutis, atrophia maculosa cutis, macular atrophy) Blepharochalasis Cutis ... Elastosis perforans serpiginosa Homocystinuria Jadassohn-Pellizzari anetoderma Linear focal elastosis (elastotic striae) Loeys- ... Reactive perforating collagenosis Schweninger-Buzzi anetoderma Sclerotic fibroma Striae atrophicans Striae distensae Ullrich ...
... comes in three types: Primary anetoderma Jadassohn-Pellizzari anetoderma is a benign condition with focal loss of ... Secondary anetoderma Familial anetoderma List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L ... Jadassohn-Pellizzari is one of two major classifications of primary anetoderma, the other being Schweninger-Buzzi anetoderma. ... Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue. ...
... Other names. (Anetoderma maculosa,[1] Anetoderma maculosa cutis,[1] Atrophia maculosa cutis,[1] and Macular atrophy ... Anetoderma comes in three types: *Primary anetoderma *Jadassohn-Pellizzari anetoderma is a benign condition with focal loss of ... the other being Schweninger-Buzzi anetoderma. The difference between the two is that Jadassohn-Pellizzari anetoderma is ... Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue.[2] ...
Anetoderma *Schweninger-Buzzi anetoderma. *Jadassohn-Pellizzari anetoderma. *Atrophoderma of Pasini and Pierini ...
Anetoderma *Schweninger-Buzzi anetoderma. *Jadassohn-Pellizzari anetoderma. *Atrophoderma of Pasini and Pierini ...
Anetoderma *Schweninger-Buzzi anetoderma. *Jadassohn-Pellizzari anetoderma. *Atrophoderma of Pasini and Pierini ...
Anetoderma. Other names. (Anetoderma maculosa,[1] Anetoderma maculosa cutis,[1] Atrophia maculosa cutis,[1] and Macular atrophy ... Anetoderma comes in three types: *Primary anetoderma *Jadassohn-Pellizzari anetoderma is a benign condition with focal loss of ... the other being Schweninger-Buzzi anetoderma. The difference between the two is that Jadassohn-Pellizzari anetoderma is ... Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue.[2] ...
Anetoderma comes in three types: Primary anetoderma Jadassohn-Pellizzari anetoderma is a benign condition with focal loss of ... Secondary anetoderma Familial anetoderma List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L ... Jadassohn-Pellizzari is one of two major classifications of primary anetoderma, the other being Schweninger-Buzzi anetoderma. ... Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue. ...
Sjögrens syndrome and cutaneous B cell lymphoma revealed by anetoderma.. Jubert C1, Cosnes A, Clerici T, Gaulard P, André P, ...
We report the first case of widespread congenital anetoderma occurring in an infant born at 24 weeks of gestation weighing 640 ... small lesions of anetoderma presenting at birth have been reported in twins born at 25 weeks of gestational age. ... Isolated, small lesions of anetoderma presenting at birth have been reported in twins born at 25 weeks of gestational age. We ... report the first case of widespread congenital anetoderma occurring in an infant born at 24 weeks of gestation weighing 640 g ...
Anetoderma, anyone? HarmonicCharge 13 years ago 8,577 C * I e-mailed you a few weeks about my son. I though... elba 13 years ... Yes, I ve had anetoderma since age 14. I search f... Bumpy1 11 years ago 7,982 * Dear Bumpy, I feel your pain! So the surgery l ... Re: Anetoderma, anyone?. Advertisement. Free Book by Dr. Clark!. Bestselling author Dr. Hulda Clark claims to have cured cancer ... Hy! Im a spanish girl who suffers from anetoderma... aina2285 10 years ago 6,994 ...
I was recently diagnosed with anetoderma after biopsy. Saw rhematogy for a full workup and was told no underlying condition or ... Re: Anetoderma, anyone?. I was recently diagnosed with anetoderma after biopsy. Saw rhematogy for a full workup and was told no ... Anetoderma, anyone? HarmonicCharge 13 years ago 8,577 C * I e-mailed you a few weeks about my son. I though... elba 13 years ... Yes, I ve had anetoderma since age 14. I search f... Bumpy1 11 years ago 7,981 * Dear Bumpy, I feel your pain! So the surgery l ...
Anetoderma: Benign DERMATOSIS caused by a loss of dermal ELASTIC TISSUE resulting in localized sac-like areas of flaccid skin. ... Anetoderma. Subscribe to New Research on Anetoderma Benign DERMATOSIS caused by a loss of dermal ELASTIC TISSUE resulting in ... Primary Anetoderma; Primary Anetodermas; Secondary Anetoderma; Secondary Anetodermas; Anetoderma, Primary ... Drugs and Important Biological Agents (IBA) related to Anetoderma: 1. AntibodiesIBA 01/01/1995 - "The finding of anetoderma in ...
Although the histopathologyof her axillary lesions was consistent with anetoderma, her clinical presentation is unusual given ... Anetoderma is a rare benign elastolytic disorder that is characterized by focal loss of elastin fibers on histopathology and is ... Anetoderma is a rare benign elastolytic disorder that is characterized by focal loss of elastin fibers on histopathology and is ... Although the histopathologyof her axillary lesions was consistent with anetoderma, her clinical presentation is unusual given ...
"Anetoderma" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... This graph shows the total number of publications written about "Anetoderma" by people in this website by year, and whether " ... Below are the most recent publications written about "Anetoderma" by people in Profiles. ...
Anetoderma is rare, but the incidence is unknown. Anetoderma has been reported in several hundred cases since the original ... The pathogenesis of anetoderma is unknown. The key defect is damage to the dermal elastic fibers. Anetoderma might be ... Primary anetoderma occurs when there is no underlying associated skin disease (i.e., it arises on clinically normal skin). It ... True secondary anetoderma implies that the characteristic atrophic lesion has appeared in the exact same site as a previous ...
Anetoderma secondary to lepromatous leprosy. Indian Journal of Leprosy. 2001 Jan-Mar; 73(1): 51-4. ...
Currently, anetoderma is classified as either primary (idiopathic) or secondary. Primary anetoderma is categorized into two ... Currently, anetoderma is classified as either primary (idiopathic) or secondary. Primary anetoderma is categorized into two ... Currently, anetoderma is classified as either primary (idiopathic) or secondary. Primary anetoderma is categorized into two ... Currently, anetoderma is classified as either primary (idiopathic) or secondary. Primary anetoderma is categorized into two ...
... in a young man with clinical and histopathologic features of primary anetoderma (Jadassohn type) of 13 years duration. ... Post-traumatic arthritis in patient with Jadassohns anetoderma DOI https://doi.org/10.4081/reumatismo.2003.48 ... Post-traumatic arthritis in patient with Jadassohns anetoderma. Reumatismo, 55(1), 48-51. https://doi.org/10.4081/reumatismo. ...
We herein, report a case of Schweninger-Buzzi type anetoderma occurring on a 6 year-old girl. The lesions did not have an ... Anetoderma is a rare cutaneous disorder characterized by circumscribed loss of skin elasticity. This has been historically ... Anetoderma Language: Korean Journal: Korean Journal of Dermatology Year: 1999 Type: Article ... Anetoderma Language: Korean Journal: Korean Journal of Dermatology Year: 1999 Type: Article ...
Regeneron Pharmaceuticals Inc said on Thursday its experimental treatment for a very rare genetic bone disorder showed a nearly 90% reduction in new lesions compared to placebo, in a mid-stage study.
Full text: Available Index: WPRIM (Western Pacific) Main subject: Arm / Skin / Actins / Anetoderma / Granuloma / Neck Language: ... Full text: Available Index: WPRIM (Western Pacific) Main subject: Arm / Skin / Actins / Anetoderma / Granuloma / Neck Language: ... Actinic Granuloma:One of the Causes of Secondary Anetoderma Kyoung-Ae JANG; Jung-Chul CHOI; Jee-Ho CHOI; Kyung-Jeh SUNG; Kee- ... Anetoderma is characterized by discrete skin lesions that appear to be loose and wrinkled. The primary type arises in ...
Anetoderma * Dermatologic Manifestations of Vitamin A Deficiency Medscape Consult. Tools. *Drug Interaction Checker ...
You can now download VisualDx for your iOS and Android devices. Launch the VisualDx app from your device and sign in using your VisualDx personal account username and password.. ...
Anetoderma. 2/2. 3. 32. Angiolymphoid hyperplasia with eosinophilia. 2/2. 3. 16. ...
Anetoderma arising in cutaneous B-cell lymphoproliferative disease.. Kasper RC, Wood GS, Nihal M, LeBoit PE. ...
... anetoderma (cutaneous macular atrophy); and Goodpastures syndrome, a severe and ultimately fatal glomerulonephritis associated ...
6465909 - Anetoderma. clinical findings, associations, and long-term follow-up evaluations.. 16178869 - Detection of apoptosis- ...
Hyperpigmentation, mild atrophy, or anetoderma may persist.. Lesions can recur after resection. The relapse rate is ...
Anetoderma *Schweninger-Buzzi anetoderma. *Jadassohn-Pellizzari anetoderma. *Atrophoderma of Pasini and Pierini ...
The differential diagnoses mainly include anetoderma, mid-dermal elastolysis, focal dermal hypoplasia, lupus panniculitis, and ...
Anetoderma associated with antiphospholipid syndrome. Jesica Martín Carmona, Elisabeth Gómez Moyano, María Ayala Blanca, ...
Anetoderma observed with reflectance confocal microscopy.. Authors: Cinotti E, Tonini G, Mancini V, Miracco C, Pellegrino M, ...
The clinical differential diagnosis includes aplasia cutis, anetoderma and atrophoderma, and atrophic DFSP.. Cutaneous and ...
Postsurgical scar with anetoderma-like herniation of the subcutaneous fat (f). Apparent absence of the lingual frenulum (g). ... traumas may hesitate in full thickness dermal atrophy with consequent subcutaneous fat herniations with anetoderma-like ...
The second issue with the shave excision is fat herniation, iatrogenic anetoderma, and hypertrophic scarring. As the deep shave ...
  • Secondary anetoderma Familial anetoderma List of cutaneous conditions Rapini, Ronald P. (wikipedia.org)
  • IMSEAR at SEARO: Anetoderma secondary to lepromatous leprosy. (who.int)
  • Currently, anetoderma is classified as either primary (idiopathic) or secondary. (elsevier.com)
  • Secondary anetoderma is associated with a variety of skin conditions, penicillamine use, or neonatal prematurity. (elsevier.com)
  • Secondary anetoderma which is oxygen is the assurance pump activity in rat and prognostic implications as. (highlandcounty.org)
  • Anetoderma secondary to the application of leeches. (elsevier.com)
  • Primary anetoderma implies that there is no associated, localized, underlying cutaneous disease, whereas true secondary anetoderma can be attributed to some associated condition though the atrophic areas do not always develop at the sites of the known inflammatory lesions. (blogspot.com)
  • To our knowledge, anetoderma secondary to hepatitis B immunization has been described only once in the literature, in two siblings vaccinated at the same time. (medscienceresearch.com)
  • [3] Jadassohn-Pellizzari is one of two major classifications of primary anetoderma, the other being Schweninger-Buzzi anetoderma . (wikipedia.org)
  • Schweninger-Buzzi anetoderma is a cutaneous condition characterized by loss of dermal elastic tissue. (wikipedia.org)
  • Primary anetoderma is categorized into two clinical types: Schweninger-Buzzi anetoderma, not preceded by erythema, and Jadassohn-Pellizari anetoderma, preceded by macular erythema. (elsevier.com)
  • Primary anetoderma has been divided into the Jadassohn-Pellizari type , in which the lesions are preceded by erythema, and the Schweninger-Buzzi type, in which there is no preceding erythema. (blogspot.com)
  • Anetoderma, also known as macular atrophy, is an unusual disease of unknown aetiology. (elsevier.com)
  • Hyperpigmentation, mild atrophy, or anetoderma may persist. (medscape.com)
  • Do you have any of these conditions: Macular Degeneration or Anetoderma or Retinal Degeneration or Dry Macular Degeneration or Geographic Atrophy or age-related macular degeneration or Dr. (centerwatch.com)
  • Some resolve without a trace, but a significant number leave skin abnormalities including residual telangiectases, atrophy, hypopigmentation, and anetoderma-like scars. (birthmark.org)
  • The term anetoderma ( Gk anetos slack ) refers to a circumscribed area of macular atrophy of the skin associated with a loss of dermal substance on palpation and a loss of elastic tissue on histopathological examination. (blogspot.com)
  • Primary anetoderma occurs when there is no underlying associated skin disease (i.e., it arises on clinically normal skin). (dermaamin.com)
  • We describe the emergence of arthritis following a physical trauma, in a young man with clinical and histopathologic features of primary anetoderma (Jadassohn type) of 13 years' duration. (reumatismo.org)
  • Case Report: Primary anetoderma with undifferentiated connective tissue disease. (sclero.org)
  • The two types of primary anetoderma can coexist in the same patient, and the prognosis and histopathology are identical in both. (blogspot.com)
  • Primary anetoderma is strongly associated with antiphospholipid antibodies with or without a prothrombotic state. (blogspot.com)
  • Diagnosis of primary anetoderma was made. (blogspot.com)
  • This finding without previous skin disease is known as primary anetoderma and is often associated with autoimmune diseases such as systemic lupus erythematosus (SLE), with antiphospholipid antibodies, and antiphospholipid syndrome (APS). (bvsalud.org)
  • The clinical differential diagnosis includes aplasia cutis, anetoderma and atrophoderma , and atrophic DFSP. (thefreedictionary.com)
  • Her skin lesions began to slowly fade 6 years after disease onset, eventually resolving spontaneously and completely, but leaving an atrophic scar, frank anetoderma, and persisting diabetes insipidus. (figshare.com)
  • We present a typical case of anetoderma which was observed in a 34-year-old male who presented with one-year history of increasing in number of well-circumscribed, normal skin-colored, soft bladder-like pouches over the back and some atrophic patches on bilateral flexor aspect of the forearms. (dermatol-sinica.com)
  • Differential diagnoses include anetoderma, annular elastolytic giant cell granuloma, cutis laxa, and pseudoxanthoma elasticum-like papillary dermal elastolysis. (renalandurologynews.com)
  • Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue . (wikipedia.org)
  • Jadassohn-Pellizzari anetoderma is a benign condition with focal loss of dermal elastic tissue. (wikipedia.org)
  • Anetoderma is a rare benign elastolytic disorder that is characterized by focal loss of elastin fibers on histopathology and is often recalcitrant to treatment. (escholarship.org)
  • Anetoderma is an infrequent elastolytic disorder, clinically characterized by areas with lack of the skin and decreased elastic fibers at histology. (bvsalud.org)
  • Anetoderma is an elastolytic disorder of unknown origin. (medscienceresearch.com)
  • Presence of the antinuclear antibodies and antibodies to Borrelia burgdorferi among patients with morphea en plaque, deep linear scleroderma and atrophoderma Pasini-Pierini. (thefreedictionary.com)
  • Other clinical entities with depressed lesions or atrophoderma include anetoderma, long-standing lupus profundus, eosinophilic fasciitis, lipodystrophy, and atrophoderma of Moulin. (renalandurologynews.com)
  • Isolated, small lesions of anetoderma presenting at birth have been reported in twins born at 25 weeks of gestational age. (biomedsearch.com)
  • Although the histopathologyof her axillary lesions was consistent with anetoderma, her clinical presentation is unusual given the extent of involvement, reported pain and pruritus, and sharp demarcation of the distribution. (escholarship.org)
  • Histopathology was consistent with anetoderma. (blogspot.com)
  • Connective tissue diseases: pseudoxanthoma elasticum, anetoderma, and Ehlers-Danlos syndrome in pregnancy. (cdc.gov)
  • Although most cases are sporadic, rare cases of familial anetoderma have been recently described and are usually not associated with preexisting lesions. (dermaamin.com)
  • Anetoderma: A rare disorder. (elsevier.com)
  • Fingerprint Dive into the research topics of 'Anetoderma: A rare disorder. (elsevier.com)
  • The second issue with the shave excision is fat herniation, iatrogenic anetoderma, and hypertrophic scarring. (wikipedia.org)
  • Sjögren's syndrome and cutaneous B cell lymphoma revealed by anetoderma. (nih.gov)
  • We report a case of perforating pilomatricoma with anetoderma in an adolescent with lymphoma. (ovid.com)
  • The differential diagnoses mainly include anetoderma, mid-dermal elastolysis , focal dermal hypoplasia, lupus panniculitis, and localized scleroderma. (thefreedictionary.com)
  • We describe a case of anetoderma that developed on the neck , both arms and calves, and showed histopathological findings of actinic granuloma . (bvsalud.org)
  • Anetoderma must be differentiated from other disorders of elastic tissue as well as atrophies of the connective tissue. (dermaamin.com)
  • Simultaneous occurrence of anetoderma in premature identical twins. (drlapidoth.com)
  • The difference between the two is that Jadassohn-Pellizzari anetoderma is preceded by inflammatory lesions. (wikipedia.org)
  • Perivascular lymphocytes are often present in all types of anetoderma and do not correlate with clinical inflammatory findings. (dermaamin.com)
  • Congenital anetoderma in a preterm infant. (biomedsearch.com)
  • We report the first case of widespread congenital anetoderma occurring in an infant born at 24 weeks of gestation weighing 640 g and discuss the potential factors in its etiology. (biomedsearch.com)
  • Anetoderma might be considered to be unusual scars, because scars also have decreased elastic tissue. (dermaamin.com)
  • All types of anetoderma are characterized by a circumscribed loss of normal skin elasticity. (dermaamin.com)
  • Anetoderma is characterized by discrete skin lesions that appear to be loose and wrinkled. (bvsalud.org)
  • Association of anetoderma with hepatitis B vaccination is speculated here, as suggested by history of vaccination two weeks prior to the onset of skin eruption and ruling out other possible causes of anetoderma. (medscienceresearch.com)
  • It may be confused with a scar, basal cell carcinoma or anetoderma. (news-medical.net)
  • Anetoderma is rare, but the incidence is unknown. (dermaamin.com)
  • In anetoderma, the lesions have a soft crinkly feel due to the significant alteration in the elastic fibers. (renalandurologynews.com)
  • By this article we report our experience about an interesting "mixed" case of anetoderma in 20-year-old girl surgically treated with the only target to improve the aesthetics reducing in this way, the clinical obviousness of the wound especially in visible part of the body like décolleté, arms and face. (elsevier.com)
  • There is also a third type of anetoderma which we might call "mixed" because the two different types appear in the same time. (elsevier.com)
  • Anetoderma has been reported in several hundred cases since the original report. (dermaamin.com)