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以霍奇金病告终的血管免疫母细胞性淋巴结病。

Angio-immunoblastic lymphadenopathy terminating as Hodgkin's disease.

作者信息

Yataganas X, Papadimitriou C, Pangalis G, Loukopoulos D, Fessas P, Papacharalampous N

出版信息

Cancer. 1977 May;39(5):2183-9. doi: 10.1002/1097-0142(197705)39:5<2183::aid-cncr2820390535>3.0.co;2-7.

Abstract

The clinical course of a 33-year-old man with generalized lymphadenopathy bearing all physical, laboratory and histologic characteristics of "angio-immunoblastic lymphadenopathy with dysproteinemia" (AILD) is described. Therapy was without significant benefit and the patient died 22 months after initial diagnosis. At autopsy in addition to the characteristic cellular polymorphism of AILD, numerous Hodgkin's cells and Sternberg-Reed cells were identified in the lymph nodes and spleen. Pleomorphic cellular infiltrates containing an increased number of immunoblasts and some giant cells were found also in the portal spaces of the liver. The evolution of Hodgkin's disease (H.D.) from AILD suggests that the latter may have represented a reaction to the agent which causes H.D..

摘要

本文描述了一名33岁患有全身淋巴结病的男性患者的临床病程,其具备“血管免疫母细胞性淋巴结病伴异常蛋白血症”(AILD)的所有体格检查、实验室及组织学特征。治疗效果不显著,患者在初诊22个月后死亡。尸检时,除了AILD典型的细胞多形性外,在淋巴结和脾脏中还发现了大量霍奇金细胞和施特恩伯格-里德细胞。在肝门区也发现了含有增多的免疫母细胞和一些巨细胞的多形性细胞浸润。AILD演变为霍奇金病(H.D.)提示,AILD可能是对导致H.D.的病原体的一种反应。

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