肺泡毛细血管发育不良伴肺静脉错位:一名足月新生儿的手术肺活检和尸检结果

Q4 Medicine
Carmen Rodríguez García, Cecilia López Valdivia, Jaime Ferrer Lozano, Nuria Mancheño Franch
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引用次数: 0

摘要

肺泡毛细血管发育不良伴肺静脉错位(ACD/MPV)是一种罕见的致死性间质性肺疾病,由影响肺实质和肺血管发育的先天性异常引起。我们报告了一例怀孕 40 周的新生儿,该新生儿在产前对照超声波检查中未发现心肺畸形。然而,在分娩后,肺动脉高压和低氧性呼吸衰竭开始显现。尽管进行了强化治疗,她还是在 12 天后死于难治性血流动力学和呼吸衰竭。对她进行了外科肺活检和临床尸检,均发现了与这种疾病一致的组织病理学征象。在我们的病例中,消化道和生殖器畸形的发现,加上 FOXF1 基因改变的遗传结果,使我们得出肺泡毛细血管发育不良的明确诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alveolar capillary dysplasia with misalignment of the pulmonary veins: A surgical lung biopsy and autopsy in a full-term newborn
Alveolar capillary dysplasia with misalignment of the pulmonary veins (ACD/MPV) is a rare and lethal interstitial lung disorder, caused by a congenital abnormality affecting the development of the parenchyma and pulmonary vessels. We report the case of a newborn at the end of 40 weeks of pregnancy, who showed no cardiopulmonary anomalies in prenatal control ultrasounds. However, after delivery, pulmonary hypertension and hypoxemic respiratory failure became apparent. She died after 12 days from refractory hemodynamic and respiratory failure despite intensive therapy. A surgical lung biopsy and clinical autopsy were performed, both revealing the same histopathological signs consistent with this disorder. In our case, the findings of digestive and genital malformations, together with the genetic result of the alteration in the FOXF1 gene, led us to conclude the definitive diagnosis of alveolar capillary dysplasia.
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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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