HYPERGAMMAGLOBULINEMIC PURPURA OF WALDENSTROM

被引:31
作者
FINDER, KA [1 ]
MCCOLLOUGH, ML [1 ]
DIXON, SL [1 ]
MAJKA, AJ [1 ]
JAREMKO, W [1 ]
机构
[1] BROOKE ARMY MED CTR, DEPT MED, DERMATOL SERV, FT SAM HOUSTON, TX 78234 USA
关键词
D O I
10.1016/0190-9622(90)70271-I
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Hypergammaglobulinemic purpura of Waldenström is characterized by hypergammaglobulinemia, recurring purpura, an elevated erythrocyte sedimentation rate, and the presence of rheumatoid factor indicative of circulating immune complexes. There is a significant association with autoimmune diseases, especially Sjögren's syndrome and lupus erythematosus, Hypergammaglobulinemic purpura is considered primary when there is no other associated disease or secondary when associated with other diseases, usually autoimmune. Immune derangements are fundamental in its pathogenesis, although its cause is still unknown. Therapy is unrewarding and is probably unnecessary for this usually benign condition. Three cases are presented that are representative of patients with hypergammaglobulinemic purpura. © 1990, American Academy of Dermatology, Inc.. All rights reserved.
引用
收藏
页码:669 / 676
页数:8
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