Korean J Dermatol.  1985 Oct;23(5):686-690.

A Case of Congenital Erythropoietic Porphyria

Abstract

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.

Keyword

Porphyria; Congenital erythropoietic

MeSH Terms

Alopecia
Anemia, Hemolytic
Anthozoa
Blood Vessels
Erythrocytes
Fluorescence
Fluorescent Antibody Technique, Direct
Hyalin
Immunoglobulin G
Microscopy
Parturition
Porphyria, Erythropoietic*
Porphyrias
Skin
Splenomegaly
Tooth
Immunoglobulin G
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