遗传性出血性毛细血管扩张症合并肺动静脉瘘和妊娠状态导致肺动脉高压加重:病例报告

Wanjiao Chen , Yuliang Long , Dandan Chen, Shengyu Hao, Lihua Guan , Daxin Zhou
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引用次数: 0

摘要

背景遗传性出血性毛细血管扩张症(HHT)是一种不常见的常染色体显性遗传病。妊娠合并 HHT 可加重肺动脉高压(PH),严重者可导致死亡。她在妊娠后三个月出现胸闷和呼吸困难,当时未引起重视,产后症状加重。超声心动图显示肺动脉压(PAP)升高,计算机断层扫描肺血管造影显示有明显的肺动静脉畸形。尽管接受了降低肺动脉高压的治疗,但患者的病情仍持续恶化。我们回顾并更新了漏诊病史、妊娠期反复鼻衄病史及其家族类似症状。结合全外显子基因检测报告,发现chr12:52308295处存在ACVRL1基因突变,HHT诊断成立。四个月后,患者接受了经导管肺动静脉瘘闭合术,结果令人满意,肺动脉压力降低了 15 毫米汞柱以上。结论肺动脉高压是一种罕见的疾病,通常与肺静脉和肺动脉之间的异常沟通同时发生,导致肺循环中的高流量状态。患者怀孕也可能引发肺动脉高压危象,进一步增加血容量。通过减少https://www.ecdc.europa.eu/sites/default/files/documents/Methods-for-the%20detection-and-characterisation-of-SARS-CoV-2-variants-first-update-WHO-20-Dec-2021.pdfg 肺血管流量,用导管关闭肺动静脉瘘可降低肺动脉压。
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Pulmonary hypertension exacerbated by hereditary hemorrhagic telangiectasia combined with pulmonary arteriovenous fistula and pregnancy status: A case report

Background

Hereditary hemorrhagic telangiectasia (HHT) is an uncommon autosomal dominant condition. The combination of pregnancy and HHT can exacerbate pulmonary hypertension (PH) and, in severe cases, lead to fatality.

Case presentation

The case we presented is a 28-year-old multiparous woman. She developed chest tightness and dyspnea in the second trimester of pregnancy, which was not taken seriously at that time, and the symptoms worsened postpartum. Echocardiography showed elevated pulmonary artery pressure (PAP) and the computerized tomographic pulmonary angiogram revealed a significant pulmonary arteriovenous malformation. The patient's condition continued to deteriorate despite treatment to reduce pulmonary hypertension. We reviewed and updated the history of omission, recurrent epistaxis during pregnancy, and similar symptoms running in her family. Combined with the whole exon genetic testing report revealing the ACVRL1 gene mutation at chr12:52308295, the diagnosis of HHT was established. Four months later, a transcatheter closure of the pulmonary arteriovenous fistula was performed, with satisfying outcomes presenting a decrease of more than 15 mmHg in the pulmonary artery pressure. As of right now, the patient's status is stable during the outpatient follow-up.

Conclusions

HHT is a rare condition that typically occurs alongside abnormal communication between pulmonary veins and arteries, leading to a high-flow state in the pulmonary circulation. A pulmonary hypertension crisis can also be triggered by the patient's pregnancy, which further increases blood volume. By reducinhttps://www.ecdc.europa.eu/sites/default/files/documents/Methods-for-the%20detection-and-characterisation-of-SARS-CoV-2-variants-first-update-WHO-20-Dec-2021.pdfg pulmonary vascular flow, catheter closure of the pulmonary arteriovenous fistula decreases pulmonary arterial pressure.

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