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阑尾先天性闭锁:一种罕见的发育异常病例。

Atresia of the appendix vermiformis: a rare case of developmental abnormality.

机构信息

Department of General Surgery, Dumlupinar University Faculty of Medicine, 43020 Kutahya, Turkey.

出版信息

World J Gastroenterol. 2013 Jan 7;19(1):122-4. doi: 10.3748/wjg.v19.i1.122.

Abstract

Acute appendicitis, which requires immediate surgical intervention, is an important diagnosis in patients with acute abdomen. However, developmental abnormalities may interfere with the preoperative diagnosis and surgical treatment in some cases. Agenesis and atresia of the cecal vermiform appendix is an extremely rare clinical diagnosis. In addition, preoperative diagnosis may be difficult in some cases. Thus, diagnosis of the congenital absence of the vermiform appendix requires a thorough exploration of the retrocecal and ileocecal regions. A 59-year-old male was admitted from the emergency services with right lower abdominal pain. A celiotomy was performed with the suspicion of acute appendicitis. However, an atresia of the vermiform appendix was observed. The patient's appendix was thus removed. Pathological examination confirmed suppurative appendicitis. This case underlines the importance of the clinical entity for surgeons who may deal with a similar case.

摘要

急性阑尾炎需要立即手术干预,是急性腹痛患者的重要诊断。然而,在某些情况下,发育异常可能会干扰术前诊断和手术治疗。回盲部阑尾未发育和闭锁是一种极为罕见的临床诊断。此外,在某些情况下术前诊断可能较为困难。因此,先天性阑尾缺如的诊断需要彻底探查回盲部和回肠末端区域。一名 59 岁男性因右下腹痛从急诊入院。剖腹探查术怀疑为急性阑尾炎。但发现阑尾闭锁。因此切除了患者的阑尾。病理检查证实为化脓性阑尾炎。这个病例强调了这种临床实体对可能遇到类似病例的外科医生的重要性。

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本文引用的文献

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Appendicitis in a duplex appendix mimicking intussusception.双阑尾阑尾炎酷似肠套叠。
BMJ Case Rep. 2010 May 11;2010:bcr12.2009.2516. doi: 10.1136/bcr.12.2009.2516.
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Duplicated appendix complicated by appendiceal cancer.阑尾重复畸形合并阑尾癌。
World J Gastroenterol. 2011 Jan 7;17(1):135-6. doi: 10.3748/wjg.v17.i1.135.
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Duplex appendicitis.复发性阑尾炎
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[Appendix vermiformis duplex--a rare surprise].[双阑尾——一个罕见的意外]
Wien Klin Wochenschr. 2005 Jul;117(13-14):492-4. doi: 10.1007/s00508-005-0390-3.
8
Atresia of the appendix.阑尾闭锁
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