| Literature DB >> 23510963 |
Bulent Baran1, Cetin Karaca, Ozlem M Soyer, Ipek Yonal, Aysun D Isiklar, Ramazan Cakmak, Meliha Nalcaci, Oner Dogan, Sabahattin Kaymakoglu.
Abstract
Rosai-Dorfman disease, formerly known as 'sinus histiocytosis with massive lymphadenopathy', is a rare self-limiting histiocytic proliferative disorder typically presenting early in life with cervical lymphadenopathy and nonspecific systemic symptoms. Although it is usually a nodal disease, extranodal lesions may be encountered in some cases. The gastrointestinal tract is uncommonly affected in Rosai-Dorfman disease and its diagnosis depends on clinical suspicion and careful histopathological examination of biopsy samples taken from involved gastrointestinal segments. Here, we report a case of atypical Rosai-Dorfman disease with systemic symptoms and diffuse gastrointestinal involvement that led to a diagnostic and therapeutic challenge.Entities:
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Year: 2013 PMID: 23510963 DOI: 10.1097/MEG.0b013e32836019f8
Source DB: PubMed Journal: Eur J Gastroenterol Hepatol ISSN: 0954-691X Impact factor: 2.566