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Eur J Gastroenterol Hepatol ; 25(7): 869-74, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23510963

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.


Subject(s)
Gastrointestinal Diseases , Histiocytosis, Sinus , Aged , Biopsy , Drug Therapy, Combination , Endoscopy, Gastrointestinal , Endosonography , Fatal Outcome , Gastrointestinal Agents/therapeutic use , Gastrointestinal Diseases/diagnosis , Gastrointestinal Diseases/therapy , Gastrointestinal Neoplasms/diagnosis , Histiocytosis, Sinus/diagnosis , Histiocytosis, Sinus/therapy , Humans , Immunosuppressive Agents/therapeutic use , Male , Predictive Value of Tests , Treatment Outcome
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