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18.97.9.170
18.97.9.170
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선천성 적혈구조혈성 포르피린증
A Case of Congenital Erythropoietic Porphyria
황종석(Jong Seok Hwang), 나건연(Gun Yoen Na), 정상립(Sang Lip Chung), 서순봉(Soon Bong Suh)
UCI I410-ECN-0102-2009-510-005423146

A 3-year-old-male had the appearance of red urine at birth and developed recurrent bullae in sun-exposed area of the skin, erythrodontia, alopecia, splenomegaly and hemolytic anemia, We observed coral red fluorescence of the teeth and urine under Wood's light and detected excessive excretion of the uroporphyrin in the urine and coproporphyrin in the stool wlth inreased porphyrin in the blood. Fluorescence of erythrocyte was demonstrated by:fluoreacence microscopy. Histologic findings showed subepidermal bulla with PAS-positive hyaline deposits around the blood vessels and revealed IgG deposits in the wall of blood vessels and dermo-epidermal junction by direct immunofluorescence.

[자료제공 : 네이버학술정보]
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