Síndrome de heterotaxia: hallazgos tomográficos

Q4 Medicine
M. Gonzalez, Luis Dibarboure
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引用次数: 0

Abstract

The objective of this brief communication is to characterize the relevant tomographic aspects in the heterotaxy syndrome, by means of 4 patients that exemplify the most frequent findings in this pathology. Situs solitus is the usual arrangement of organs and blood vessels and situs inversus refers to the mirror image of situs solitus. When the arrangement of the organs is indeterminate and unpredictable and does not correspond to situs solitus or the situs inversus, we are facing the situs ambiguus or heterotaxy syndrome, abnormal spectrum of anomalies in the relations of the thoracoabdominal organs. It may be accompanied by right isomerism or left isomerism. Attempts to classify it into two subgroups are usually difficult since none of these has unique and pathognomonic findings, but rather there is broad overlap. Both are of poor prognosis, in the cases of left isomerism 5-10% reach adulthood, with a worse prognosis being the cases of right isomerism due to the fact that they have immunodepression secondary to asplenia and more severe congenital cardiopathies. Each case should be analyzed in an individualized and detailed manner to establish the diagnosis, determine the lesional association and establish those patients that present a higher risk of complications.
这篇简短的交流的目的是通过4例在这种病理中最常见的发现的患者来描述异位综合征的相关断层扫描方面。静位是器官和血管的正常排列,逆位是指静位的镜像。当脏器的排列是不确定的和不可预测的,不对应于孤立位置或倒置位置时,我们面临的是位置模糊或异位综合征,胸腹器官关系异常的异常谱。可伴有右同分异构体或左同分异构体。试图将其分为两个亚组通常是困难的,因为这些亚组都没有独特的病理特征,而是有广泛的重叠。两者预后都很差,左同分异构体患者的预后为5-10%,右同分异构体患者的预后较差,因为他们有继发于脾功能不全的免疫抑制和更严重的先天性心脏病。每个病例都应以个性化和详细的方式进行分析,以确定诊断,确定病变关系,并确定哪些患者存在较高的并发症风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Revista Argentina de Radiologia
Revista Argentina de Radiologia Medicine-Radiology, Nuclear Medicine and Imaging
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