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孤立性单侧肺动脉缺如伴肺动脉高压的手术治疗。

Surgical treatment of isolated unilateral absence of pulmonary artery with pulmonary hypertension.

机构信息

Department of Cardiovascular Surgery, Osaka Women's and Children's Hospital, Osaka, Japan.

出版信息

Cardiol Young. 2021 Aug;31(8):1371-1372. doi: 10.1017/S104795112100069X. Epub 2021 Mar 8.

DOI:10.1017/S104795112100069X
PMID:33682647
Abstract

A one-and-a-half-month-old patient with isolated unilateral absence of the right proximal pulmonary artery with prominent left pulmonary hypertension was diagnosed using CT. Medication therapy was initiated first. Left pulmonary artery pressure decreased after the initiation of medication therapy, and single-stage reconstruction of the right pulmonary artery was performed. The patient is asymptomatic 14 months postoperatively.

摘要

一位一个半月大的婴儿,孤立性右侧肺动脉近端缺如,伴有明显的左侧肺动脉高压,经 CT 诊断。首先进行药物治疗。药物治疗开始后,左肺动脉压下降,随后进行了右肺动脉一期重建。术后 14 个月,患者无症状。

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Surgical treatment of isolated unilateral absence of pulmonary artery with pulmonary hypertension.孤立性单侧肺动脉缺如伴肺动脉高压的手术治疗。
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Effective control of refractory pulmonary hypertension with iloprost inhalation in an infant with congenital absence of the right pulmonary artery: a case report.婴儿先天性右肺动脉缺如致难治性肺动脉高压,吸入伊洛前列素治疗有效:病例报告。
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