| Literature DB >> 19262248 |
Anu Maheshwari1, Anju Seth, Monisha Choudhury, Varun Aggarwal, Bijoy Patra, Shilpi Aggarwal, Sharmila B Mukherjee, Satinder Aneja.
Abstract
Rosai-Dorfman disease (RDD), originally described as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic proliferative disorder with a distinctive microscopic appearance. Formerly thought to be a disease process limited to lymph nodes, RDD has now been reported in many organ systems like bone, skin and soft tissue, central nervous system, eye and orbit, and upper respiratory tract. Here we report a case of RDD with hepatic involvement, which is even more rare.Entities:
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Year: 2009 PMID: 19262248 DOI: 10.1097/MPH.0b013e31818e5369
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289