医学
窦组织细胞增生伴大量淋巴结病变
罗赛-多夫曼病
磁共振成像
组织细胞增多症
活检
放射科
窦(植物学)
疾病
病理
植物
生物
属
作者
Richard Woodcock,James W. Mandell,Maurice H. Lipper
出处
期刊:Radiology
[Radiological Society of North America]
日期:1999-12-01
卷期号:213 (3): 808-810
被引量:85
标识
DOI:10.1148/radiology.213.3.r99dc30808
摘要
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.
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