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呼吸道合胞病毒肺炎患儿中肺泡毛细血管发育不良伴肺静脉错位的不寻常表现:一例报告。

Unusual presentation of alveolar capillary dysplasia with misalignment of the pulmonary veins in a child with respiratory syncytial virus pneumonia: A case report.

作者信息

Sirianansopa Kantisa, Prasertsan Pharsai, Ruangnapa Kanokpan, Saelim Kantara, Kor-Anantakul Phawin

机构信息

Division of Pulmonology and Critical Care Medicine, Department of Pediatrics, Faculty of Medicine Prince of Songkla University Songkhla Thailand.

Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, and Department of Pediatrics, Faculty of Medicine Chulalongkorn University Bangkok Thailand.

出版信息

Respirol Case Rep. 2023 Jan 26;11(2):e01089. doi: 10.1002/rcr2.1089. eCollection 2023 Feb.

Abstract

Alveolar capillary dysplasia with misalignment of the pulmonary veins (ACDMPV) is a rare congenital diffuse lung disorder, with a fatal course during the neonatal period. We describe an 18-month-old boy who presented with respiratory syncytial virus pneumonia and pulmonary hypertensive crisis requiring extracorporeal membrane oxygenation. Exome sequencing revealed a frameshift variant, NM_001451.2:c.995_998delACTC, inherited from his asymptomatic mother. Genetic findings were compatible with histopathology findings from a lung biopsy. Based on the disease course, histopathology, and outcomes of this case, we believe ACDMPV should be considered a possibility in an infant presenting with hypoxemic respiratory failure, resistant pulmonary hypertension, and vasodilator-induced pulmonary edema. Genetic testing can contribute to the diagnostic process.

摘要

肺泡毛细血管发育不良伴肺静脉错位(ACDMPV)是一种罕见的先天性弥漫性肺部疾病,在新生儿期有致命病程。我们描述了一名18个月大的男孩,他因呼吸道合胞病毒肺炎和肺动脉高压危象而需要体外膜肺氧合。外显子组测序发现了一个移码变异,NM_001451.2:c.995_998delACTC,遗传自他无症状的母亲。基因检测结果与肺活检的组织病理学结果相符。基于该病例的病程、组织病理学和结果,我们认为对于出现低氧性呼吸衰竭、难治性肺动脉高压和血管扩张剂诱导的肺水肿的婴儿,应考虑ACDMPV的可能性。基因检测有助于诊断过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ea7/9880384/9710922bf86b/RCR2-11-e01089-g003.jpg

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