Intussusception of the appendix secondary to endometriosis: a case report.

IF 0.7 Q4 SURGERY
Yuta Kawaguchi, Kyoichiro Maekawa, Toshiaki Hashimoto, Mizuki Kitagawa, Shigetoshi Urabe, Emi Yoshimura, Takashi Goto, Mihoko Rikitake, Tohru Iwata
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Abstract

Background: Intussusception of the appendiceal endometriosis is rare. Although approximately 200 cases of appendiceal intussusception have been reported in the literature, very few have ever been diagnosed preoperatively. Here, we report the case of intussusception of the appendiceal endometriosis with laparoscopic ileocecal resection.

Case presentation: A woman in her 50s presented to the out-patients clinic with epigastric pain lasting for a several month. Contrast-enhanced computed tomography (CT) scanning revealed ileocolic intussusception in which a cecum polypoid mass lesion extended to the hepatic flexure of the ascending colon. A colonoscopy showed a large pedunculated polyp in the cecum. Laparoscopic ileocecal resection was performed. Pathology confirmed an invaginated appendix demonstrating endometriosis implants.

Conclusions: Possible intrinsic causes of intussusception are varied, appendiceal intussusception secondary to endometriosis is extremely rare. Intussusception of the appendix is a rare finding, often mistaken for a polyp. We suggest considering inverted appendix as a differential diagnosis when investigating cecal lesions.

子宫内膜异位症继发阑尾闭锁:病例报告。
背景:阑尾子宫内膜异位症肠套叠非常罕见。尽管文献中已报道了约 200 例阑尾内膜异位症肠套叠病例,但术前确诊的病例却寥寥无几。在此,我们报告了一例阑尾子宫内膜异位症肠套叠腹腔镜回盲部切除术的病例:一名 50 多岁的妇女因持续数月的上腹痛到门诊就诊。造影剂增强计算机断层扫描(CT)显示回结肠肠套叠,其中盲肠息肉状肿块病变延伸至升结肠肝曲。结肠镜检查显示盲肠内有一个巨大的有蒂息肉。患者接受了腹腔镜回盲肠切除术。病理证实阑尾内陷,显示有子宫内膜异位症植入物:阑尾闭锁的内在原因多种多样,但继发于子宫内膜异位症的阑尾闭锁极为罕见。阑尾闭锁是一种罕见的发现,常常被误认为是息肉。我们建议在检查盲肠病变时将倒置盲肠作为鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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