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遗传性球形红细胞增多症脾切除术二十年。

Twenty years of splenectomy for hereditary spherocytosis.

作者信息

Rutkow I M

出版信息

Arch Surg. 1981 Mar;116(3):306-8. doi: 10.1001/archsurg.1981.01380150034008.

Abstract

A retrospective study of all patients who underwent splenectomy during the 20-year period, 1960 to 1979, for hereditary spherocytosis at the Johns Hopkins Hospital, Baltimore, identified 58 patients, of whom 20 (33%) were 15 years of age or older. Accessory splenic tissue was located in ten (17%) of the patients. Although cholelithiasis was present in only 12 (21%) of the total cohort, when analyzed for patients 10 years of age or older the incidence was 41% (11/27). Because of the positive association between advancing age, cholelithiasis, and hereditary spherocytosis, it is recommended that any patient 10 years of age or older undergo an oral cholecystogram as part of the routine preoperative evaluation.

摘要

一项对1960年至1979年这20年间在巴尔的摩约翰霍普金斯医院因遗传性球形红细胞增多症接受脾切除术的所有患者进行的回顾性研究,确定了58例患者,其中20例(33%)年龄在15岁及以上。10例(17%)患者发现有副脾组织。虽然整个队列中只有12例(21%)存在胆结石,但在对10岁及以上患者进行分析时,发病率为41%(11/27)。由于年龄增长、胆结石与遗传性球形红细胞增多症之间存在正相关,建议任何10岁及以上的患者进行口服胆囊造影,作为常规术前评估的一部分。

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