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Case Reports
. 2024 Jun 30;62(275):471-473.
doi: 10.31729/jnma.8648.

Linear Atrophoderma of Moulin: A Case Report

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Case Reports

Linear Atrophoderma of Moulin: A Case Report

Anu Duwal et al. JNMA J Nepal Med Assoc. .

Abstract

Linear Atrophoderma of Moulin is a rare skin condition that is characterized by the development of one or more atrophic patches or depressions in the skin. These patches are usually located on the trunk, but they can also occur on the arms, legs, and neck. We here present a case of 33-year Nepalese male with brown to black color lesions over the left upper back, abdomen and thigh for the last 7 years. Clinical and dermatopathological findings were similar to the Linear Atrophoderma of Moulin. To our knowledge, this is the first case of LAM from Nepal. This case emphasizes the necessity of diagnosing Atrophoderma of Moulin and separating it from linear scleroderma due to differences in therapy and prognosis.

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Conflict of interest statement

The author declared no competing interests.

Figures

Figure 1
Figure 1. A) Hyperpigmented patches were observed on the left side of the abdomen, and left iliac region, B) Similar lesions on the left upper back and posterolateral aspect of left arm, C) Similar lesions over to the medial aspect of left thigh.
Figure 2
Figure 2. A) Hematoxylin-eosin stain. The epidermis was acanthotic with pigmented basal layer. Dermis had sclerotic collagen with high-up eccrine glands with loss of peri-eccrine fat and sparse perivascular lymphocytic infiltrate, B) Same slide in 100X.

References

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