| Literature DB >> 10742418 |
M D Fiel-Gan1, T M Voytek, R G Weiss, R T Brown, V V Joshi.
Abstract
Castleman's disease (CD) is histologically characterized by a proliferation of polyclonal small lymphocytes and plasma cells. The clinical presentation varies widely, but most commonly manifests as a solitary mediastinal mass, incidentally found on radiographic examination. We present a case of a 10-year-old girl who exhibited a left arm mass which, preoperatively and on frozen section, was diagnosed as a small round cell tumor of childhood (SRCT). This report emphasizes the unusual location of CD in the soft tissue and as a rare entity to be considered in the differential diagnosis of SRCT.Entities:
Mesh:
Year: 2000 PMID: 10742418 DOI: 10.1007/s100249910038
Source DB: PubMed Journal: Pediatr Dev Pathol ISSN: 1093-5266