| A Clinical Study on Histiocytosis Syndromes: Review of Ten Cases
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Y.K. Chang, Y.W. Hong, B.H. Rie, J.Y . Choi, C.Y. Hong |
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Department of Pediatrics, College of Medicine, Seoul National University |
| Histiocytosis 振候群의 臨皮的 觀察
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張永吉, 洪錯字, 李街動, 崔奏榮, 李街動 |
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서울大學校 醫科大學 小兒科學敎室 |
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| Abstract |
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Ten cases of Histiocytosis syndromes who had been admitted to Seoul National University Hospital from 1960 to 1968 were reviewed.1. One case belongs to group I, five cases to group II and four cases to group III Sex ratio: male to female was 6 : 4. 2. Age onset ranged from 2. 5 months to five years, average 3. 5 years in group I, 2. 5 years in
group II , and 1. 5 years in group III. 3.Only ane case in group I showed the all signs included in. triad exophthalmos, polyuria, and skull defects. 4.Three quarters of patients in group III had dermatitis, hepatosplenomegaly, lymphnode swelling and anemia. 5. A case belongs to group HI showed lung infiltration at the onset. 6. Bone lesions were main characteristic in group I and group II. Calvarial defects in group II revealed in all cases. Prednisone was effective pn bone lesions. 7.All cases in group III died.
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