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SCOPUS
과 호산구 증후군
A Case of Hypereosinophilic Syndrome
박세준 , 김재준 , 김재홍 ( Se Hoon Park , Jae Joon Kim , Jae Hong Kim )
UCI I410-ECN-0102-2009-510-005444169

The hypereosinophilic syndrome consists of peripheral blood eosinophilia of 1500/ mm3 or more without a known cause, plus signs and symptoms of organ eosinophilia. We report a case of hypereosnophilic syndrome with cutaneous manifestation. A 31 year-old female had intermittent fever, sbdominal pain, anemia, systolic murmur, hepatosplenomegaly, cheat discomfort, dry cough without rales, and skin-colored wheal on the trunk. Diagnoais of hypereosinophilic syndrome wss established by clinical findings, marked blood eosinophilia without a known cause, bone marrow aspiration and biopsy, liver scan, and histopsthologic findings of the skin.

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