2013
DOI: 10.1159/000346747
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Linear Atrophoderma of Moulin:A Case Report and Review of the Literature

Abstract: Linear atrophoderma of Moulin (LAM) is a rare dermatosis in childhood and early adolescence. The exact etiology of LAM is still obscure. Several treatment modalities were reported but none was consistently successful. We report a case of LAM in which a favorable outcome was obtained with topical calcipotriol. The relevant literature is also reviewed.

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Cited by 18 publications
(21 citation statements)
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“…A partial response to topical calcipotriol was reported. 7 A case of LAM successfully treated with methotrexate 20 mg/wk for 6 months with an improvement of pigmentation and atrophy was reported. 8 The authors suggested that LAM, atrophoderma of Pasini and Pierini, and linear scleroderma may be a spectrum of a common disease entity in view of the response to methotrexate, which is an effective therapeutic option for morphea.…”
Section: Discussionmentioning
confidence: 99%
“…A partial response to topical calcipotriol was reported. 7 A case of LAM successfully treated with methotrexate 20 mg/wk for 6 months with an improvement of pigmentation and atrophy was reported. 8 The authors suggested that LAM, atrophoderma of Pasini and Pierini, and linear scleroderma may be a spectrum of a common disease entity in view of the response to methotrexate, which is an effective therapeutic option for morphea.…”
Section: Discussionmentioning
confidence: 99%
“…[1] Postzygotic mutation in lamin A gene has been postulated as a possibility for developing this disorder. [2] The trunk and limbs are usually involved without any preceding inflammation or subsequent induration and sclerosis.…”
mentioning
confidence: 99%
“…[4] However, subcutaneous tissue is not routinely mentioned to be reduced according to other reports and text. [12] LAM is a self-limited disease. Progression of the lesions usually stops within a few months without any pattern of remission.…”
mentioning
confidence: 99%
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