Zain Mostafa, Abada Mohamed, Abouheba Mohamed, Elrouby Ahmed, Ibrahim Amir
Department of Pediatric Surgery, Faculty of Medicine, University of Alexandria, Egypt.
Int J Surg Case Rep. 2020;70:123-125. doi: 10.1016/j.ijscr.2020.04.066. Epub 2020 May 11.
Acute intrathoracic gastric volvulus occurs when the stomach undergoes organoaxial rotation in the chest due presence of a diaphragmatic defect. Gastric volvulus associated with congenital diaphragmatic hernia is extremely rare and can be explained as 2 of the 4 ligaments supporting the stomach (gastrophrenic and gastrosplenic) which are connected to the left diaphragm may become elongated or absent. According to the current literature, only 27 pediatric cases have been reported so far.
We describe an 8 years old boy who presented to our emergency department with acute epigastric pain and vomiting. The chest radiograph obtained in the emergency department demonstrated an elevated gastric air-fluid level in the left hemithorax. A computed tomography scan demonstrated a sizable left diaphragmatic defect admitting stomach, small bowel loops and transverse colon with organoaxial gastric volvulus. Emergent laparotomy was done for reduction of the viscera to the abdominal cavity and repair of the diaphragmatic defect. The patient showed an uneventful recovery without experience any pain or difficulty with eating.
Acute gastric volvulus is a rare pathology defined as an abnormal rotation of the stomach for more than 180° leading to a closed-loop obstruction which may progress to ischemia and strangulation. A plain standing abdominal X-ray and an upper gastrointestinal contrast study are useful for diagnosis, but some authors recommend performing CT or MRI to confirm the diagnosis. The standard treatment for volvulus is open laparotomy with detorsion and anterior gastropexy.
The presented case highlights congenital diaphragmatic hernia associated with gastric volvulus is a serious condition with very high morbidity and mortality. It should be considered in the differential diagnosis of children with epigastric pain and uncontrolled non bilious vomiting. An upper gastrointestinal contrast study is useful for early diagnosis and surgical treatment should not be delayed awaiting further complementary imaging tests.
当胃因存在膈肌缺损而在胸腔内发生器官轴旋转时,就会出现急性胸内胃扭转。与先天性膈疝相关的胃扭转极为罕见,这可以解释为支撑胃的4条韧带中的2条(胃膈韧带和胃脾韧带)与左膈肌相连,可能会变长或缺失。根据目前的文献,迄今为止仅报道了27例儿科病例。
我们描述了一名8岁男孩,他因急性上腹部疼痛和呕吐前来我院急诊科就诊。急诊科拍摄的胸部X光片显示左半胸胃内气液平面升高。计算机断层扫描显示有一个较大的左膈肌缺损,胃、小肠袢和横结肠由此进入胸腔,伴有器官轴型胃扭转。紧急进行剖腹手术,将内脏回纳至腹腔并修复膈肌缺损。患者恢复顺利,未出现任何疼痛或进食困难。
急性胃扭转是一种罕见的病理情况,定义为胃异常旋转超过180°,导致闭环梗阻,可能进展为缺血和绞窄。立位腹部X线平片和上消化道造影检查有助于诊断,但一些作者建议进行CT或MRI以确诊。胃扭转的标准治疗方法是开放剖腹手术,进行扭转复位和前胃固定术。
该病例突出表明,先天性膈疝合并胃扭转是一种严重疾病,发病率和死亡率极高。对于有上腹部疼痛和无法控制的非胆汁性呕吐的儿童,应考虑此病。上消化道造影检查有助于早期诊断,不应等待进一步的补充影像学检查而延迟手术治疗。