Roy Pankaj G, Patel Prerna, Vayalakkad Anitha, Bowker Colene, Lakhoo Kokila
Department of Paediatric Surgery, John Radcliffe hospital, Oxford OX3 9DU, UK.
Pediatr Surg Int. 2007 Sep;23(9):915-7. doi: 10.1007/s00383-007-1904-z.
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.
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。