Rare presentation of spontaneous acquired diaphragmatic hernia.
نویسندگان
چکیده
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.
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ورودعنوان ژورنال:
- The Indian journal of chest diseases & allied sciences
دوره 53 2 شماره
صفحات -
تاریخ انتشار 2011