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首页> 外文期刊>American Journal of Case Reports >A Rare Case of Bochdalek Hernia with Concomitant Para-Esophageal Hernia, Repaired Laparoscopically in an Octogenarian
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A Rare Case of Bochdalek Hernia with Concomitant Para-Esophageal Hernia, Repaired Laparoscopically in an Octogenarian

机译:罕见的Bochdalek疝伴伴食管旁疝的病例,通过腹腔镜手术修复

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Patient: Male, 81 Final Diagnosis: Bochdalex hernia Symptoms: Chest pain ? vomiting Medication: — Clinical Procedure: Laparoscopic repair of both diaphragmatic hernias Specialty: Surgery Objective: Rare co-existance of disease or pathology Background: A Bochdalek hernia (BH) is a rare congenital condition consisting of a posterolateral defect in the diaphragm. A para-esophageal hernia (PEH) is a rare variant of hiatus hernia. BH and PEH may present with gastric volvulus or incarceration, requiring emergency treatment. Minimally invasive surgery is the preferred treatment, particularly for elderly patients and patients with comorbidities. The occurrence of BH with concomitant PEH is a very rare event. We describe a case of an octogenarian patient with BH and concomitant PEH treated laparoscopically. Case Report: An 81-year-old male patient, without significant comorbidities, presented with a two-month history of severe chest pain and vomiting after eating. Cardiological investigations ruled out cardiac ischemia, infarction, or other cardiovascular abnormalities. Chest and abdominal computed tomography (CT) imaging demonstrated a large diaphragmatic hernia, with the entire stomach in the left thorax. Laboratory results showed mild anemia and a low iron level. The patient underwent simultaneous laparoscopic repair of a BH and a PEH with mesh reinforcement without antireflux fundoplication. The patient’s postoperative recovery was uneventful. Conclusions: We have presented a rare case of BH with concomitant PEH in an octogenarian that was successfully treated with laparoscopic surgery. Although these two forms of hernia are a very rare association, this case report illustrates that the surgical approach should be individualized in each patient’s case to ensure a successful surgical outcome. In this case, the decision was made to suture the diaphragmatic crura and reinforce the diaphragm repair with mesh, rather than by fundoplication.
机译:患者:男性,81岁最终诊断:Bochdalex疝气症状:胸痛?呕吐药物:—临床程序:腹腔镜修复两个diaphragm肌疝专长:手术目的:罕见的疾病或病理并存背景:博克达莱克疝(BH)是一种罕见的先天性疾病,由the肌后外侧缺损组成。食管旁疝(PEH)是裂孔疝的一种罕见变体。 BH和PEH可能伴有胃扭转或嵌顿,需要紧急治疗。微创手术是首选治疗方法,特别是对于老年患者和合并症患者。 BH伴有PEH的发生是非常罕见的事件。我们描述了一个BH和伴随PEH的八十岁患者的腹腔镜治疗病例。病例报告:一名81岁的男性患者,无明显合并症,有两个月的严重胸痛和进食后呕吐史。心脏病学调查排除了心脏缺血,梗塞或其他心血管异常。胸部和腹部计算机断层扫描(CT)图像显示大diaphragm肌疝,整个胃位于左胸腔。实验室结果显示轻度贫血和铁水平低。该患者同时接受腹腔镜修补BH和PEH,并进行网状加固,而无抗反流胃底折叠术。患者的术后恢复情况良好。结论:我们介绍了一个罕见的BH伴有PEH的八面体患者,该病例成功地通过腹腔镜手术治疗。尽管这两种形式的疝气非常罕见,但该病例报告表明,应根据每个患者的情况对手术方法进行个性化设置,以确保成功的手术结果。在这种情况下,决定缝合the肌并用网而不是通过胃底折叠术来加强the肌修复。

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