自发性后天性膈疝的罕见表现。

Rare presentation of spontaneous acquired diaphragmatic hernia.

作者信息

Gupta Shweta, Bali Roseleen Kaur, Das Kamanasish, Sisodia Anula, Dewan R K, Singla Rupak

机构信息

Department of Tuberculosis and Respiratory Diseases, L.R.S. Institute of Tuberculosis and Respiratory Diseases, New Delhi, India.

出版信息

Indian J Chest Dis Allied Sci. 2011 Apr-Jun;53(2):117-9.

PMID:21545075

Abstract

Spontaneous acquired diaphragmatic hernia without any apparent history of trauma is a very rare condition and is very difficult to diagnose. We present a case of a 21-year-old male who presented with abdominal pain for one month and four episodes of vomiting for one day. Clinical suspicion, chest radiography with nasogastric tube in situ and computed tomography (CT) confirmed the diagnosis. The diaphragmatic defect was repaired surgically. The patient had an uneventful post-operative recovery.

摘要

无明显创伤史的自发性后天性膈疝是一种非常罕见的病症，诊断极为困难。我们报告一例21岁男性患者，其腹痛1个月，呕吐4次，持续1天。临床怀疑，结合置入鼻胃管的胸部X线检查及计算机断层扫描（CT）确诊。通过手术修复了膈肌缺损。患者术后恢复顺利。