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镰状细胞病患儿的脾脏功能:沙特阿拉伯的两种不同模式。

Splenic function in children with sickle cell disease: two different patterns in Saudi Arabia.

作者信息

Babiker M A, el-Hazmi M A, Al-Jobori A M, Obeid H, Bahakim H M

出版信息

Scand J Haematol. 1985 Aug;35(2):191-3. doi: 10.1111/j.1600-0609.1985.tb01570.x.

Abstract

Splenic function in 35 Saudi children homozygous for sickle cell disease (age range 3-9 years) was studied using radioactive colloid scans. Two different patterns emerged. Splenic dysfunction was demonstrated in more than 80% of children who were originally from the south-western part of the country. They were found to have low HbF levels. In contrast normal or nearly normal splenic function was found in all patients from the Eastern Province in whom HbF levels were high. These different patterns of splenic function may contribute to the severe and mild forms of sickle cell disease seen in Saudi Arabia.

摘要

利用放射性胶体扫描研究了35名患有镰状细胞病的沙特纯合子儿童(年龄范围3至9岁)的脾脏功能。出现了两种不同的模式。在该国西南部地区的80%以上儿童中表现出脾脏功能障碍。他们的HbF水平较低。相比之下,在东部省份所有HbF水平较高的患者中发现脾脏功能正常或接近正常。脾脏功能的这些不同模式可能导致了沙特阿拉伯所见的镰状细胞病的严重和轻度形式。

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