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卡马西平治疗过程中发生致命性粒细胞缺乏症。病例报告及文献综述。

Fatal agranulocytosis developed in the course of carbamazepine therapy. A case report and review of the literature.

作者信息

Olcay L, Pekcan S, Yalnizoğlu D, Büyükpamukçu M, Yalaz K

机构信息

Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

Turk J Pediatr. 1995 Jan-Mar;37(1):73-7.

PMID:7732613
Abstract

A case of fatal agranulocytosis in an adolescent who was on carbamazepine therapy is presented. The clinical and laboratory findings suggest that the primary cause of the disorder was neutropenia rather than infection, and the preceding factor for neutropenia was carbamazepine. The timing of occurrence of the hematologic picture, its dependency on dose increments, and the lack of symptoms until infection supervened are consistent with an idiosyncratic-toxic drug reaction (type 2 drug reaction). This is the first reported agranulocytosis case due to crabamazepine in adolescence.

摘要

本文报告了一例接受卡马西平治疗的青少年发生致命性粒细胞缺乏症的病例。临床和实验室检查结果表明,该疾病的主要病因是中性粒细胞减少而非感染,中性粒细胞减少的先前因素是卡马西平。血液学表现出现的时间、对剂量增加的依赖性以及在感染发生前缺乏症状,均符合特异质毒性药物反应(2型药物反应)。这是首次报道的青少年因卡马西平导致的粒细胞缺乏症病例。

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