Literature DB >> 23996873

A case of isolated cutaneous Rosai-Dorfman-Syndrome.

M M Rizwan1, G Chhabra, A Mishra, S Kapadia, R Rai, H Gill.   

Abstract

UNLABELLED: Rosai-Dorfman Syndrome (RDD) is a rare, benign, self-limiting disorder which is characterized by the non-malignant proliferation of distinctive histiocytic cell within lymphatic system. RDD has been described as a dynamic entity in the spectrum of histiocytosis with non-Langerhans cell histiocytosis at one end and Langerhans cell histiocytosis at the other. The exact etiology of this disease is uncertain despite widespread search for infectious or immunological reasons. We present a case of purely cutaneous Rosai-Dorfman Syndrome presenting as abdominal wall swelling. KEYWORDS: Rosai-Dorfman Disease, Lymphoma.

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Year:  2013        PMID: 23996873

Source DB:  PubMed          Journal:  Gulf J Oncolog        ISSN: 2078-2101


  1 in total

1.  Histological variability and the importance of clinicopathological correlation in cutaneous Rosai-Dorfman disease.

Authors:  Ana Gameiro; Miguel Gouveia; José Carlos Cardoso; Oscar Tellechea
Journal:  An Bras Dermatol       Date:  2016 Sep-Oct       Impact factor: 1.896

  1 in total

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