| Autor: |
Ertop Doğan, Pelin, Topuz, Merve, Hazinedar, Emel, Doğan Gün, Banu, Türk, Yaşar, Koca, Rafet |
| Předmět: |
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| Zdroj: |
International Journal of Dermatology; Aug2024, Vol. 63 Issue 8, p1102-1104, 3p |
| Abstrakt: |
Linear atrophoderma of Moulin (LAM) is a rare dermatological condition characterized by unilateral hyperpigmented and atrophic band-like skin lesions following Blaschko's lines. The exact cause of LAM is unclear, but it is believed to be related to either autoimmunity or genetic mosaicism. This article describes a case of LAM in a 27-year-old man, highlighting a granulomatous reaction and antinuclear-antibody (ANA) positivity. The patient's chronic lesions met the diagnostic criteria for LAM, except for a thinner dermis and subcutaneous tissue. The article also discusses the dermoscopic features, treatment options, and the potential link between LAM and autoimmunity or connective tissue diseases. [Extracted from the article] |
| Databáze: |
Complementary Index |
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