| A case of Epidermolysis Bullosa Hereditaria Simplex |
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S.K. Kim1, K.C Nam1, S.H Shin1, K.J Kim1, D.K Chung2 |
1Department of Pediatric, Jeonju Jesus Hospital
2Department of Clinical Pathology, Jeonju Jesus Hospital |
| 遺傳性 單純性 表皮水胞症 1例 |
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김석곤1, 남기종1, 신성희1, 김기준1, 정동규2 |
1전주예수병원 소아과
2임상병리과 |
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| Abstract |
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The authors report a child who has a kindred affected with epidermolysis bullosa hereditaria
simplex over 5 generations.
Diagnosis was made on the. basis of family history, clinical maifestations, and histological findings
of the affected skin. The absence of dystrophic changes of the skin and mucous membrane is characteristic
of this tybe and gives a better prognosis than the dystrophis form. Trauma and moisture
should be avoided as possible, since it may induce new lesions. The chloroquine has been being made
an attempt in this case during warm weather, on the basis of passage’s report which the chloroquine
sulfate is effective in prevention and delaying of new lesions and treatment of the epidermolysis
bullosa simplex.
We are observing the results whether the chloroquine sulfate could prevent or delay deveolpment
of the new lesions associated with trauma, as Passage mentioned.
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