医学
肝脾肿大
代谢亢进
淋巴瘤
细胞淋巴瘤
病理
骨髓
脾脏
霍奇金淋巴瘤
淋巴系统
内科学
疾病
作者
J. Donald,Nick Barnthouse,Delphine L. Chen
出处
期刊:Clinical Nuclear Medicine
[Ovid Technologies (Wolters Kluwer)]
日期:2018-04-01
卷期号:43 (4): e125-e126
被引量:5
标识
DOI:10.1097/rlu.0000000000001969
摘要
Abstract Intravascular lymphoma (IVL) is a rare subtype of diffuse large B-cell lymphoma characterized by a clonal proliferation of lymphocytes restricted to the intravascular space. We present the case of a 60-year-old man with hemophagocytic syndrome secondary to IVL. 18 F-FDG PET/CT demonstrated hepatosplenomegaly with marked diffuse hepatic, splenic, and bone marrow hypermetabolism. The case report illustrates the imaging findings of this uncommon variant of IVL.
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