Bifid Vermiform Appendix: A Case Report

Ewen A. Griffiths, Jayaraman Jagadeesan, Tarannum Fasih, Mark Mercer-Jones
{"title":"Bifid Vermiform Appendix: A Case Report","authors":"Ewen A. Griffiths,&nbsp;Jayaraman Jagadeesan,&nbsp;Tarannum Fasih,&nbsp;Mark Mercer-Jones","doi":"10.1016/j.cursur.2006.02.001","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Appendiceal anomalies are extremely rare: they have a reported incidence of between 0.004% and 0.009% of appendectomy specimens. The authors report a case of a patient who was found to have 2 appendices at emergency laparotomy, review the classification system used, and discuss the potential clinical pitfalls of similar cases.</p></div><div><h3>Case Report</h3><p>A 23-year-old man was admitted as an emergency with abdominal pain and vomiting. The operative finding was of a bifid appendix. One appendix was grossly gangrenous and lacked a mesoappendix, whereas the other had a mesoappendix and appeared macroscopically normal. The appendices shared a common base that arose from the cecum in the typical anatomical position. No other intra-abdominal malformations were present at inspection during laparotomy. Histology confirmed features of gangrenous appendicitis. His postoperative recovery was uneventful, and he was discharged after 4 days.</p></div><div><h3>Conclusion</h3><p>Although rare, it is important for several reasons that surgeons are aware of the potential anatomical anomalies and malpositions of the vermiform appendix: first, a missed second appendix may result in serious clinical and medico-legal consequences; second, a double appendix can be confused with other intra-abdominal conditions; and finally, they can be associated with other congenital abnormalities.</p></div>","PeriodicalId":75762,"journal":{"name":"Current surgery","volume":"63 3","pages":"Pages 176-178"},"PeriodicalIF":0.0000,"publicationDate":"2006-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.cursur.2006.02.001","citationCount":"24","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0149794406000225","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 24

Abstract

Introduction

Appendiceal anomalies are extremely rare: they have a reported incidence of between 0.004% and 0.009% of appendectomy specimens. The authors report a case of a patient who was found to have 2 appendices at emergency laparotomy, review the classification system used, and discuss the potential clinical pitfalls of similar cases.

Case Report

A 23-year-old man was admitted as an emergency with abdominal pain and vomiting. The operative finding was of a bifid appendix. One appendix was grossly gangrenous and lacked a mesoappendix, whereas the other had a mesoappendix and appeared macroscopically normal. The appendices shared a common base that arose from the cecum in the typical anatomical position. No other intra-abdominal malformations were present at inspection during laparotomy. Histology confirmed features of gangrenous appendicitis. His postoperative recovery was uneventful, and he was discharged after 4 days.

Conclusion

Although rare, it is important for several reasons that surgeons are aware of the potential anatomical anomalies and malpositions of the vermiform appendix: first, a missed second appendix may result in serious clinical and medico-legal consequences; second, a double appendix can be confused with other intra-abdominal conditions; and finally, they can be associated with other congenital abnormalities.

双虫形附录:1例报告
阑尾异常极为罕见:据报道,其发生率在0.004%至0.009%的阑尾切除术标本之间。作者报告了一例在急诊剖腹手术中发现有两个阑尾的患者,回顾了所使用的分类系统,并讨论了类似病例的潜在临床陷阱。病例报告一名23岁男子因腹痛和呕吐急诊入院。手术发现为双尾。一个阑尾严重坏疽,缺乏阑尾系膜,而另一个有阑尾系膜,宏观上看起来正常。阑尾有一个共同的基底,起源于盲肠,处于典型的解剖位置。剖腹检查时未见其他腹内畸形。组织学证实为坏疽性阑尾炎。术后恢复顺利,4天后出院。结论蚓状阑尾虽然罕见,但由于以下几个原因,外科医生必须意识到蚓状阑尾的潜在解剖异常和错位:第一,第二阑尾的遗漏可能导致严重的临床和法医学后果;其次,双阑尾可能与其他腹内疾病混淆;最后,它们可能与其他先天性异常有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信