Angio-immunoblastic lymphadenopathy terminating as Hodgkin's disease.

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..

journal_name

Cancer

journal_title

Cancer

authors

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

doi

10.1002/1097-0142(197705)39:5<2183::aid-cncr282039

subject

Has Abstract

pub_date

1977-05-01 00:00:00

pages

2183-9

issue

5

eissn

0008-543X

issn

1097-0142

journal_volume

39

pub_type

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