Linear atrophoderma of Moulin: A rare case report and review of the literature

Author:

Hussein Al‐janabi Moatasem1,Diab Sdrah2,Aljammal Ghina3,Kassab Lina2,Al‐Shehabi Zuheir1,Al‐Soiufi Lina4

Affiliation:

1. Department of Pathology Cancer Research Center Tishreen University Hospital Lattakia Syria

2. Department of Dermatology and Sexually Transmitted Disease Tishreen University Hospital Lattakia Syria

3. Faculty of Medicine in Damascus University Damascus Syria

4. Department of Dermatology National Hospital Lattakia Syria

Abstract

AbstractLinear 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. We report a rare case of LAM in an 18‐year‐old female presenting with an atypical Blaschkoid distribution (multiple band‐like pattern) on her right trunk. A clinical examination and histopathological analysis were performed to make the diagnosis. Partial improvement was obtained with calcipotriol and colchicine. LAM is a rare condition; we were only able to identify 23 case reports in the published literature. The findings of this report contribute to the limited literature on LAM, highlighting the clinical variability of LAM and suggesting potential novel variants beyond the classic presentation, emphasising the importance of recognising diverse manifestations for accurate diagnosis and management. Early recognition of LAM is crucial for appropriate treatment and improved patient outcomes. Further research is needed to elucidate LAM's aetiology and underlying mechanisms to facilitate the development of more targeted therapeutic strategies.

Publisher

Wiley

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