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成人 Uhl 氏异常。

Uhl's Anomaly in Adulthood.

机构信息

Department of Critical Care Medicine, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.

Department of Adult Congenital Heart Disease, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.

出版信息

World J Pediatr Congenit Heart Surg. 2024 Jul;15(4):523-525. doi: 10.1177/21501351241236720. Epub 2024 May 2.

Abstract

Uhl's anomaly is a rare congenital syndrome characterized by the absence of right ventricular myocardium. The widely accepted pathological mechanism is intrauterine myocardial apoptosis. Uhl's syndrome carries a poor prognosis. In rare situations, patients with Uhl's anomaly reach adulthood. We will present a case of a 29-year-old patient with Uhl's syndrome treated at our center, highlighting the diagnostic, surgical, and postoperative challenges in management.

摘要

乌尔曼异常是一种罕见的先天性综合征,其特征为右心室心肌缺如。被广泛接受的病理机制为宫内心肌细胞凋亡。乌尔曼综合征预后不良。在极少数情况下,乌尔曼异常患者可存活至成年。我们将报告一例在我院治疗的 29 岁乌尔曼综合征患者,重点介绍诊断、手术和术后管理方面的挑战。

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引用本文的文献

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Cardiac transplantation as resolution for Uhl's anomaly: A case report.心脏移植治疗乌尔氏畸形:一例报告。
JHLT Open. 2025 Jul 11;9:100343. doi: 10.1016/j.jhlto.2025.100343. eCollection 2025 Aug.

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