| Literature DB >> 16501845 |
Houda Alatassi1, Mukunda B Ray, Susan Galandiuk, Sunati Sahoo.
Abstract
Rosai-Dorfman disease (RDD) is a rare, acquired disease of unknown etiology that affects primarily children and young adults. It is characterized by a proliferation of distinctive histiocytes in the lymph nodes and/or extranodal sites. Involvement of the gastrointestinal tract is rare. We report a case of RDD in a 60-year-old woman who presented with hematochezia and was found to have RDD of the rectum presenting as a rectal mass. This report highlights the current pathogenetic mechanisms, immunohistochemical markers, and the gastrointestinal manifestations of RDD. Int J Surg Pathol 14(1):95-99, 2006.Entities:
Mesh:
Substances:
Year: 2006 PMID: 16501845 DOI: 10.1177/106689690601400119
Source DB: PubMed Journal: Int J Surg Pathol ISSN: 1066-8969 Impact factor: 1.271