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| http://dx.doi.org/10.5021/ad.2018.30.1.116 | DOI Listing |
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Linear Atrophoderma of Moulin: A Case Report.
JNMA J Nepal Med Assoc
June 2024
Department of Family Medicine, Nepal Armed Police Force Hospital, Kathmandu, Nepal.
Article Synopsis
- Linear Atrophoderma of Moulin (LAM) is a rare skin condition marked by atrophic patches on the skin, primarily on the trunk, but can also appear on the arms, legs, and neck.
- A case study presented involves a 33-year-old male from Nepal who has had brown to black lesions on his left upper back, abdomen, and thigh for 7 years, with findings consistent with LAM.
- This case is notable as it is the first documented instance of LAM in Nepal and highlights the importance of distinguishing it from linear scleroderma for appropriate treatment and prognosis.
Linear atrophoderma of Moulin (LAM) is an uncommon dermatological disease characterised by linear, depressed plaques typically following Blaschko's lines. LAM generally occurs in adolescence or early adulthood and is more commonly observed in females. The aetiology of LAM is still unclear.
View Article and Find Full Text PDFLinear atrophoderma of Moulin.
J Dermatol
June 2024
Dermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Roma, Italy.
Clinical and dermoscopic findings of linear atrophoderma of Moulin: a case with an autoimmune and inflammatory background.
Int J Dermatol
August 2024
Dermatology Department, Faculty of Medicine, Zonguldak Bulent Ecevit University, Zonguldak, Turkey.
BULGARIAN PATIENT WITH ATROPHODERMA OF PASINI AND PIERINI- DESCRIPTION OF A CASE AND SHORT UPDATE.
Georgian Med News
November 2023
1Onkoderma - Clinic for Dermatology, Venereology and Dermatologic Surgery, Sofia, Bulgaria; 4Department of Dermatology and Venereology, Medical Institute of Ministry of Interior, Sofia, Bulgaria.
Article Synopsis
- Atrophoderma of Pasini and Pierini is a rare, benign skin condition characterized by single or multiple asymptomatic atrophic plaques, predominantly affecting women of European descent, usually appearing in their 20s or 30s.
- Recent reports suggest a potential link between this condition and COVID-19, with a notable case of rapid progression post-infection observed in a 63-year-old female patient who was initially misdiagnosed with morphea.
- Accurate diagnosis relies on histopathological verification and clinical examination, as the condition often resembles morphea and may lead to treatment delays if not correctly identified.
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