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移植物抗宿主病所致中毒性表皮坏死松解症。发生于一名胸腺发育不全患者。

Toxic epidermal necrolysis from graft-vs-host disease. Occurrence in a patient with thymic hypoplasia.

作者信息

McCarty J R, Raimer S S, Jarratt M

出版信息

Am J Dis Child. 1978 Mar;132(3):282-4. doi: 10.1001/archpedi.1978.02120280066013.

Abstract

An infant with diarrhea, failure to thrive, and a seborrhea-like skin eruption was thought to have fatal familial Leiner's syndrome. Treatment with nonirradiated plasma was followed by graft-vs-host disease and fatal toxic epidermal necrolysis; thymic hypoplasia was found at autopsy. Accurate diagnosis of immunodeficiency syndromes is essential to avoid potentially harmful therapy.

摘要

一名患有腹泻、发育不良和脂溢性皮炎样皮疹的婴儿被认为患有致命的家族性莱纳综合征。用未辐照血浆治疗后出现移植物抗宿主病和致命的中毒性表皮坏死松解症;尸检发现胸腺发育不全。准确诊断免疫缺陷综合征对于避免潜在的有害治疗至关重要。

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