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SCLEROMYXEDEMA
Journal Title Acta Medica Iranica
Journal Abbreviation acta
Publisher Group Tehran University of Medical Sciences (TUMS)
Website http://acta.tums.ac.ir
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Title SCLEROMYXEDEMA
Authors Z. Safaii Naraghi., ; P. Mansouri M.R. Mortazavi,
Abstract Scleromyxedema is a rare, chronic, progressive, fibromucinous disorder of unknown etiology, characterized by lichenoid waxy papules and firm induration of skin of trunk, face, forearm and hands; fibroblast proliferation and mucin deposition in the upper dermis. Cutaneous involvement is characteristic but there are several associated systemic manifestations: We observed a case of scleromyxedema with multiple systemic manifestations including endocrinopathy and hypothyroidism. Scleromyxedema is a multisystem disorder associated with multiple organ involvement including liver, muscle, kidney and could be associated with endocrinopathies including hypothyroidism.
Publisher Tehran University of Medical Sciences
Date 2012-10-20
Source Acta Medica Iranica Vol 34, No 3-4 (1996)

 

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