| Literature DB >> 20620063 |
Jia-Tang Zhang1, Hui-Jun Tian, Sen-Yang Lang, Xiang-Qin Wang.
Abstract
Sinus histiocytosis with massive lymphadenopathy (SHML), also known as Rosai-Dorfman disease (RDD), is an idiopathic histiocytic disorder of lymph nodes and extranodal sites. Central nervous system (CNS) manifestations, particularly in the absence of nodal disease, are rare. Intracranial RDD clinically and radiologically resembles meningioma, and histologic examination is essential for a definitive diagnosis. We report four patients with RDD primary to the CNS without evidence of other sites of involvement, review the literature, and discuss the clinical manifestations, pathology, treatment and outcome. Crown Copyright 2010. Published by Elsevier Ltd. All rights reserved.Entities:
Mesh:
Year: 2010 PMID: 20620063 DOI: 10.1016/j.jocn.2010.01.048
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961