A Brief Review of Scalp Biopsy and its Interpretation. [PDF]
Gowda SK, Behera B, Sethy M, Ayyanar P.
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Combination of intravenous immunoglobulin, oral prednisone, and methotrexate for managing scleromyxedema: case report and literature discussion. [PDF]
Fasano G +3 more
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Pediatric CD4+ Small Medium Sized Pleomorphic T-cell Lymphoproliferative Disorder: A Unique Indolent Lymphoproliferative Lesion With Consistent Reproducible Clinical and Phenotypic Features. [PDF]
Li X, Magro CM.
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Desmosomal-Type Acantholysis-A New Histologic Pattern Related to Mutations of Genes for Desmosomal Proteins. [PDF]
Metze D +4 more
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Reticular erythematous mucinosis
AbstractReticular erythematous mucinosis is a rare syndrome which can be misdiagnosed as seborrhoeic dermatitis. This long‐lasting skin disease, which is characterized by the histological presence of deposits of mucin in the dermis, usually responds to treatment with per os hydroxychloroquine, 400 mg/day, for 3 months.
T. Lotti, M. Benci, B. Lorusso
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Reticular Erythematous Mucinosis Occurring in a Brother and Sister
Reticular erythematous mucinosis (REM) is a rare, primary cutaneous mucinosis clinically characterized by a persistent reticular erythema on the mid chest and mid-upper back, and histologically by a mononuclear cell infiltrate and deposits of mucin in the dermis. To our knowledge, the present report of REM occurring in a Caucasian man and his sister is
R. Caputo +3 more
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Reticular erythematous mucinosis – (REM syndrome) in twins
JDDG - Journal of the German Society of Dermatology, 2009SummaryWe present female twins with reticular erythematous mucinosis (REM syndrome). Remarkably, the lesions developed in both sisters almost at the same time in the same locations after UV exposure. Reports of familial manifestations of REM syndrome are very rare and an association to a distinct HLA constellation has not been proven.
Maren, Fühler +2 more
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Reticular erythematous mucinosis and thrombocytopenic purpura
Suzanne W. Braddock +2 more
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Reticular Erythematous Mucinosis Syndrome
Two female patients had eruptions with the morphologic and histologic features of reticular erythematous mucinosis syndrome. However, both cases had features that differed from previous descriptions. In one case the eruption developed three to four weeks after a single erythemogenic sun exposure and faded after two to three weeks.
Warwick L. Morison
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