Linear Atrophoderma of Moulin: A Rare Blaschkoid Dermatosis

Linear atrophoderma of Moulin (LAM) is a rare, benign dermatosis characterized by unilateral, hyperpigmented, slightly atrophic plaques distributed along Blaschko’s lines. We report the case of an 18-year-old woman with a four-year history of asymptomatic lesions on the right abdomen, thigh, and foot. Histopathology revealed basal layer hyperpigmentation, mild collagen thickening, and a sparse perivascular lymphocytic infiltrate, without sclerosis. The clinical and histological findings confirmed the diagnosis of LAM. Given the stable course and absence of symptoms, a conservative approach with follow-up was adopted. This case underscores the importance of recognizing LAM’s distinctive presentation to avoid unnecessary treatments.

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Publication Details

Journal
Dermato
Published
2025-11-29
DOI
https://doi.org/10.3390/dermato5040022
Primary Topic
Genetic and rare skin diseases.
Type
article
Field-Weighted Citation Impact
0.00
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article

Linear Atrophoderma of Moulin: A Rare Blaschkoid Dermatosis

Emilio Berná‐Rico, Luis Alonso‐Mtz de Salinas
Dermato
Genetic and rare skin diseases.
article

Linear Atrophoderma of Moulin: A Rare Blaschkoid Dermatosis

Emilio Berná‐Rico, Luis Alonso‐Mtz de Salinas
article en

Abstract

Linear atrophoderma of Moulin (LAM) is a rare, benign dermatosis characterized by unilateral, hyperpigmented, slightly atrophic plaques distributed along Blaschko’s lines. We report the case of an 18-year-old woman with a four-year history of asymptomatic lesions on the right abdomen, thigh, and foot. Histopathology revealed basal layer hyperpigmentation, mild collagen thickening, and a sparse perivascular lymphocytic infiltrate, without sclerosis. The clinical and histological findings confirmed the diagnosis of LAM. Given the stable course and absence of symptoms, a conservative approach with follow-up was adopted. This case underscores the importance of recognizing LAM’s distinctive presentation to avoid unnecessary treatments.

DermatoVol. 5(4)
Instituto Cajal (ES), Hospital Universitario Ramón y Cajal (ES)
Openalex Percentile: Top 60%
Genetic and rare skin diseases.
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