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一名成年患者的胸腹裂孔疝

Pleuroperitoneal Hernia in an Adult Patient.

作者信息

Rodríguez Mario R, González Juan S, Alfonso Karen L, Becerra Paula A, Gaviria María C, Herrera Ortiz Andrés Felipe

机构信息

Fundación Universitaria Juan N Corpas, Bogotá, Colombia.

Universidad El Bosque, Bogotá, Colombia.

出版信息

Perm J. 2021 Dec 14;25:21.055. doi: 10.7812/TPP/21.055.

Abstract

INTRODUCTION

Pleuroperitoneal hernia is the most frequent diaphragmatic congenital hernia, appearing in 1 in 3,000 births. This diaphragmatic defect is located on the left side in 80% to 90% of cases. Pleuroperitoneal hernia is usually diagnosed in the first 8 weeks of life due to respiratory compromise caused by the herniation of abdominal organs into the thoracic cavity; therefore, adult presentation is a rare condition.

CASE PRESENTATION

We present a case of a 55-year-old man with a history of long-term cigarette smoking who arrived at the emergency department with a chronic cough. Initially, the patient was misdiagnosed as exacerbated chronic obstructive pulmonary disease, for which a contrast chest computed tomography was performed showing a left posterior pleuroperitoneal hernia that contained the upper pole of the ipsilateral kidney and adrenal fatty tissue. The surgical approach chosen in this case was through laparoscopy, resulting in an appropriate postsurgical evolution, for which the patient was discharged with a general surgery control appointment. The patient was evaluated 1 week and 1 month after surgery, showing a normal physical examination and resolution of the respiratory symptoms.

CONCLUSION

Pleuroperitoneal hernia symptoms in adults most commonly affect the gastrointestinal and the respiratory tract. The diagnosis is performed by computed tomography or magnetic resonance imaging, in which a diaphragmatic defect can be seen. Pleuroperitoneal hernia complications must always be discarded by computed tomography and transthoracic echocardiogram. The treatment is based on surgical repair of the diaphragmatic defect. The surgical approach chosen may vary according to the surgeon's expertise.

摘要

引言

胸腹裂孔疝是最常见的先天性膈疝,在每3000例出生中出现1例。这种膈缺损在80%至90%的病例中位于左侧。胸腹裂孔疝通常在出生后的前8周内被诊断出来,原因是腹腔器官疝入胸腔导致呼吸功能受损;因此,成人发病是一种罕见情况。

病例报告

我们报告一例55岁男性,有长期吸烟史,因慢性咳嗽到急诊科就诊。最初,患者被误诊为慢性阻塞性肺疾病加重,为此进行了胸部增强计算机断层扫描,显示左侧后胸腹裂孔疝,疝内容物为同侧肾脏上极和肾上腺脂肪组织。本例选择的手术方法是腹腔镜手术,术后恢复良好,患者出院时预约了普通外科复诊。术后1周和1个月对患者进行了评估,体格检查正常,呼吸道症状消失。

结论

成人胸腹裂孔疝症状最常影响胃肠道和呼吸道。通过计算机断层扫描或磁共振成像进行诊断,可发现膈缺损。必须通过计算机断层扫描和经胸超声心动图排除胸腹裂孔疝并发症。治疗基于膈缺损的手术修复。选择的手术方法可能因外科医生的专业技能而异。

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