Rais-Bahrami K, Gilbert J C, Hartman G E, Chandra R S, Short B L
Department of Neonatology, George Washington University School of Medicine, Washington, District of Columbia, USA.
Am J Perinatol. 1996 May;13(4):241-3. doi: 10.1055/s-2007-994372.
We describe an infant with severe eventration of the right diaphragm and pulmonary hypoplasia who presented like a newborn with congenital diaphragmatic hernia complicated by persistent pulmonary hypertension. Surgical correction while on extracorporeal life support was unsuccessful due to attachments of the liver which prevented reduction into the abdominal cavity and our inability to distinguish the true defect from complete agencies of the right hemidiaphragm. At autopsy the pulmonary remnant and the fibrous membrane separating it from the liver were identified.
我们描述了一名患有严重右侧膈膨出和肺发育不全的婴儿，其表现如同患有先天性膈疝并伴有持续性肺动脉高压的新生儿。在体外生命支持下进行手术矫正未成功，原因是肝脏的附着妨碍了将其回纳至腹腔，且我们无法将真正的缺损与右侧半膈完全缺如区分开来。尸检时确定了肺残余组织以及将其与肝脏分隔开的纤维膜。
