血管免疫母细胞性淋巴结病：病例报告

Angioimmunoblastic lymphadenopathy: a case study.

作者信息

Kessler E

出版信息

Cancer. 1976 Oct;38(4):1587-90. doi: 10.1002/1097-0142(197610)38:4<1587::aid-cncr2820380424>3.0.co;2-d.

DOI:10.1002/1097-0142(197610)38:4<1587::aid-cncr2820380424>3.0.co;2-d

Abstract

The case of a 57-year-old man with lymphadenopathy fever, splenomegaly, and polyclonal gammopathy is described. The difficult clinical course, the short lived response to cytotoxic treatment, the frequent infections, the immunologic abnormality, and the histologic findings in lymph node biopsy and postmortem material justified our diagnosis of angioimmunoblastic lymphadenopathy with dysproteinemia, a new entity described recently.

摘要

本文描述了一名57岁男性患者，伴有淋巴结病、发热、脾肿大和多克隆丙种球蛋白病。其艰难的临床病程、对细胞毒性治疗的短暂反应、频繁感染、免疫异常以及淋巴结活检和尸检材料中的组织学发现，证实了我们对伴有蛋白异常血症的血管免疫母细胞性淋巴结病这一最近描述的新疾病实体的诊断。