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以气胸为表现的肺泡毛细血管发育不良:一例病例报告及文献复习

Alveolar capillary dysplasia presenting as pneumothorax: a case report and review of literature.

作者信息

Roy Pankaj G, Patel Prerna, Vayalakkad Anitha, Bowker Colene, Lakhoo Kokila

机构信息

Department of Paediatric Surgery, John Radcliffe hospital, Oxford OX3 9DU, UK.

出版信息

Pediatr Surg Int. 2007 Sep;23(9):915-7. doi: 10.1007/s00383-007-1904-z.

Abstract

Alveolar capillary dysplasia, although rare, is a universally fatal form of persistent pulmonary hypertension of the newborn. We report a case of a newborn male baby who developed respiratory distress and pneumothorax 11 h after an uncomplicated delivery. He deteriorated despite full ventilatory support and extracorporeal membrane oxygenation (ECMO). Open lung biopsy provided a diagnosis of alveolar capillary dysplasia and decision was made to withdraw treatment.

摘要

肺泡毛细血管发育不良虽然罕见,但却是新生儿持续性肺动脉高压的一种普遍致命形式。我们报告一例男婴,其在顺产无并发症11小时后出现呼吸窘迫和气胸。尽管给予了充分的通气支持和体外膜肺氧合(ECMO)治疗,他的病情仍恶化。开胸肺活检诊断为肺泡毛细血管发育不良,并决定停止治疗。

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