| Literature DB >> 10580957 |
R J Woodcock1, J W Mandell, M H Lipper.
Abstract
Sinus histiocytosis with massive lymphadenopathy (SHML) is an uncommon disorder that typically manifests as systemic symptoms and lymphadenopathy. Extranodal, intracranial disease is uncommon. The authors report on a 15-year-old adolescent girl who had a suprasellar mass at magnetic resonance imaging. Biopsy results demonstrated lymphophagocytosis consistent with a diagnosis of SHML. The clinical, radiologic, and histologic aspects of the disease are discussed.Entities:
Mesh:
Year: 1999 PMID: 10580957 DOI: 10.1148/radiology.213.3.r99dc30808
Source DB: PubMed Journal: Radiology ISSN: 0033-8419 Impact factor: 11.105