Ma Youngeun, Jang Mi Ae, Yoo Hye Soo, Ahn So Yoon, Sung Se In, Chang Yun Sil, Ki Chang Seok, Park Won Soon
Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Laboratory Medicine and Genetics, Soonchunhyang University Bucheon Hospital, Soonchunhyang University College of Medicine, Bucheon, Korea.
Yonsei Med J. 2017 May;58(3):672-675. doi: 10.3349/ymj.2017.58.3.672.
Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is an autosomal dominant, fatal developmental disorder of the lungs, with a mortality rate of about 100%. ACD/MPV is caused by mutations in FOXF1. Herein, we describe a newborn boy with ACD/MPV carrying a novel pathogenic variant of FOXF1. The patient developed respiratory distress and severe pulmonary hypertension on the first day of life. Despite aggressive cardiorespiratory management, including veno-venous extracorporeal membrane oxygenation, his condition deteriorated rapidly, and he died within the first month of his life. Lung histology showed the characteristic features of ACD/MPV at autopsy. Sequence analysis of FOXF1 from genomic DNA obtained from autopsied lung tissue revealed that the patient was heterozygous for a novel missense variant (c.305T>C; p.Leu102Pro). Further analysis of both parents confirmed the de novo occurrence of the variant. To the best of our knowledge, this is the first report of genetically confirmed ACD/MPV in Korea.
肺泡毛细血管发育不良伴肺静脉异位引流(ACD/MPV)是一种常染色体显性遗传的致命性肺部发育障碍疾病,死亡率约为100%。ACD/MPV由FOXF1基因突变引起。在此,我们描述了一名患有ACD/MPV的男婴,其携带FOXF1基因的一种新型致病变体。该患者在出生第一天就出现了呼吸窘迫和严重的肺动脉高压。尽管采取了积极的心肺管理措施,包括静脉-静脉体外膜肺氧合,但他的病情迅速恶化,在出生后第一个月内死亡。尸检时肺组织学显示出ACD/MPV的特征性表现。对从尸检肺组织获得的基因组DNA进行FOXF1序列分析发现,该患者为一种新型错义变体(c.305T>C;p.Leu102Pro)的杂合子。对其父母的进一步分析证实了该变体的新发情况。据我们所知,这是韩国首例经基因确诊的ACD/MPV报告。