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一例罕见的儿童白塞病合并慢性血栓栓塞性肺动脉高压病例。

A rare childhood case of Behcet's disease and chronic thromboembolic pulmonary hypertension.

作者信息

Wang Amy S, Rosenzweig Erika B, Takeda Koji

机构信息

Division of Pediatric Cardiology, Columbia University Irving Medical Center, New York, New York.

出版信息

J Card Surg. 2020 Jul;35(7):1669-1672. doi: 10.1111/jocs.14610. Epub 2020 May 17.

DOI:10.1111/jocs.14610
PMID:32419255
Abstract

BACKGROUND

Pulmonary embolism and chronic thromboembolic pulmonary hypertension (CTEPH) are rare complications of Behcet's disease, especially in pediatric patients.

AIMS/METHODS/RESULTS/CONCLUSIONS: This case report highlights a presentation of CTEPH in an adolescent with Behcet's disease. A multidisciplinary approach was required for managing this patient's CTEPH, which successfully reversed the patient's pulmonary hypertension.

摘要

背景

肺栓塞和慢性血栓栓塞性肺动脉高压(CTEPH)是白塞病罕见的并发症,尤其是在儿科患者中。

目的/方法/结果/结论:本病例报告重点介绍了一名患有白塞病的青少年患者出现CTEPH的情况。管理该患者的CTEPH需要多学科方法,该方法成功逆转了患者的肺动脉高压。

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