A Case of Hypergammaglobulinemic Purpura of Waldenstrom / 대한피부과학회지
Korean Journal of Dermatology
;
: 789-793, 1995.
Article
in Korean
| WPRIM
| ID: wpr-77725
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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Purpura
/
Purpura, Hyperglobulinemic
/
Rheumatoid Factor
/
Autoimmune Diseases
/
Vasculitis
/
Blood Sedimentation
/
Sjogren's Syndrome
/
Follow-Up Studies
/
Hypergammaglobulinemia
Type of study:
Observational study
/
Prognostic study
/
Risk factors
Limits:
Female
/
Humans
Language:
Korean
Journal:
Korean Journal of Dermatology
Year:
1995
Type:
Article
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