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先天性膈疝在胃镜检查时并发张力性胃胸腔:一例报告

Congenital diaphragmatic hernia complicated by tension gastrothorax during gastroscopy: report of a case.

作者信息

Ninos Anestis, Felekouras Evagelos, Douridas Gerasimos, Ajazi Enkel, Manataki Anna, Pierrakakis Stefanos, Setakis Nikolaos

机构信息

Department of Surgery, Thriassion General Hospital, 18 Levidiou Street, 131.21 Ilion, Athens, Greece.

出版信息

Surg Today. 2005;35(2):149-52. doi: 10.1007/s00595-004-2875-5.

Abstract

Bochdalek's hernia typically manifests early in childhood, but it is uncommon in adults. We report the case of a 77-year-old woman who suffered sudden acute cardiorespiratory distress during an upper gastro-intestinal endoscopy, caused by a massive gastrothorax, confirmed by a chest radiograph and thoracic computed tomography. Laparotomy revealed a posterolateral diaphragmatic defect and an acutely distended stomach occupying the left hemithorax, caused by an incomplete organoaxial volvulus of the organ. The stomach was reduced and secured inside the abdominal cavity by a Nissen fundoplication and the defect was repaired with interrupted sutures. Unfortunately, the patient succumbed to generalized sepsis resulting from Pneumocystis carinii bilateral pneumonia. To our knowledge, this is the first reported case in the English literature of an adult with a congenital posterolateral hernia presenting in this manner. However, it demonstrates that a symptomatic congenital diaphragmatic hernia should be surgically repaired to prevent the numerous complications that may arise, many of which can prove fatal even in an adult.

摘要

博赫达勒克疝通常在儿童期早期出现,但在成人中并不常见。我们报告一例77岁女性病例,该患者在上消化道内镜检查期间突然出现急性心肺窘迫,原因是巨大胃胸,胸部X线片和胸部计算机断层扫描证实了这一点。剖腹手术发现后外侧膈肌缺损,胃急性扩张占据左半胸,这是由器官不完全的器官轴扭转引起的。通过nissen胃底折叠术将胃复位并固定在腹腔内,缺损用间断缝合修复。不幸的是,患者死于卡氏肺孢子虫双侧肺炎引起的全身感染。据我们所知,这是英文文献中首次报道的以这种方式出现的先天性后外侧疝的成人病例。然而,它表明有症状的先天性膈疝应进行手术修复,以预防可能出现的众多并发症,其中许多并发症即使在成人中也可能是致命的。

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