A Case of Hypergammaglobulinemic Purpura of Waldenstrom.
- Author:
Myeong Kyoo LIM
;
Ho Sun JANG
;
Kyung Sool KWON
;
Tae Ahn CHUNG
- Publication Type:Case Report
- Keywords:
Hypergammaglobulinemic purpura of Waldenstrom
- MeSH:
Autoimmune Diseases;
Blood Sedimentation;
Female;
Follow-Up Studies;
Humans;
Hypergammaglobulinemia;
Middle Aged;
Purpura;
Purpura, Hyperglobulinemic*;
Rheumatoid Factor;
Sjogren's Syndrome;
Vasculitis
- From:Korean Journal of Dermatology
1995;33(4):789-793
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Hypergammaglobulinemic purpura of Waldenstrom is characterized by recurrent episodes of petechiae, hypergammaglobulinemia, an elevated erythrocyte sedimentation rate, and the presence of rheumatoid factor, and leukocytoclastic vasculitis or mild lymphocytic perivasculitis. There is a primary type and a secondary type which is associated with other autoimmune diseases. We present a csae of a 48 year-old female with hypergammaglobulinemic purpura of Waldenstrom. She showed characteristic clinical, histopathological and laboratory findings consistent with hypergammaglobulinema purpura of Waldenstrom. Although there was a decrease in the Schimer test, we couldt den ostrate an association with Sjogrens syndrome. We think that this case may be a secondary type and needs a follow-up study.
