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患儿行左侧股动脉置管后偶然发现梅-图二氏综合征。

May-Thurner syndrome found incidentally after left femoral catheterization in a pediatric patient.

机构信息

Department of Anesthesiology, Paik Hospital, Inje University, Busan, Korea.

出版信息

Pediatr Blood Cancer. 2010 Dec 1;55(6):1191-4. doi: 10.1002/pbc.22595.

Abstract

In May-Thurner syndrome, the left common iliac vein is compressed between the overlying right common iliac artery and the underlying vertebral body. Chronic and/or repetitive compressions at this site cause fibrosis of the vein and thus stenosis, potentially occluding the lumen. This report describes a case of May-Thurner syndrome discovered incidentally after femoral catheterization for chemotherapy in a 25-month-old child with juvenile myelomonocytic leukemia (JMML). The patient had no symptoms associated with compression. The syndrome was diagnosed by computed tomography, and there was no evidence of thrombosis. The patient died secondary to sepsis.

摘要

在 May-Thurner 综合征中,左髂总静脉位于上方的右髂总动脉和下方的椎体之间。该部位的慢性和/或反复压迫导致静脉纤维化,从而引起狭窄,可能导致管腔闭塞。本报告描述了一例 25 个月大的 JMML 患儿在接受化疗的股动脉导管插入术后偶然发现的 May-Thurner 综合征病例。该患者没有与压迫相关的症状。该综合征通过计算机断层扫描诊断,没有血栓形成的证据。该患者继发于脓毒症死亡。

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