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与MZ蛋白酶抑制剂表型相关的严重化疗相关性肝毒性。

Severe chemotherapy-related hepatic toxicity associated with MZ protease inhibitor phenotype.

作者信息

Ruchelli E D, Horn M, Taylor S R

机构信息

Department of Pathology, Children's Hospital of Pittsburgh, Pennsylvania.

出版信息

Am J Pediatr Hematol Oncol. 1990 Fall;12(3):351-4. doi: 10.1097/00043426-199023000-00019.

Abstract

We describe a 10 1/2-month-old boy in whom fulminant hepatic failure following chemotherapy for Wilms' tumor developed. He then received an orthotopic liver transplant. An unexpected finding was the accumulation of alpha 1-antitrypsin (AAT) in periportal hepatocytes. A pretransplant serum sample showed a Pi MZ phenotype. The rarity of hepatic failure following treatment for Wilms' tumor raises the possibility of an increased susceptibility to toxic injury in the presence of AAT accumulation. Determination of the frequency of protease inhibitor MZ phenotype in patients who have chemotherapy-related hepatotoxicity could be used to initiate a prospective study aimed at identifying an at-risk population for chemoradiotherapy-related hepatoxicity.

摘要

我们描述了一名10个半月大的男孩,他在接受肾母细胞瘤化疗后出现暴发性肝衰竭。随后他接受了原位肝移植。一个意外发现是α1抗胰蛋白酶(AAT)在汇管区周围肝细胞中蓄积。移植前血清样本显示为Pi MZ表型。肾母细胞瘤治疗后发生肝衰竭的罕见性增加了在存在AAT蓄积时对毒性损伤易感性增加的可能性。测定化疗相关肝毒性患者中蛋白酶抑制剂MZ表型的频率,可用于启动一项前瞻性研究,旨在确定放化疗相关肝毒性的高危人群。

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