Case report: A rare presentation of right illiac fossa pain

Abida Sultana *, Ahmed Saad, Yan Mei Goh, Kyi Toe
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Abstract

Introduction

Duplex appendix is a rare congenital abnormality with an incidence of 2 in 50,000. Incidences of duplex appendicitis are a rare but recognised phenomenon. Unusual presentation of this congenital abnormality can lead to delays in diagnosis and management.

Case description

A 42-year-old male presented with a two-day history of right iliac fossa pain and raised inflammatory markers. He underwent diagnostic laparoscopy where a normal appendix was seen. Laparoscopic appendicectomy was not performed. He represents several years later with similar symptoms and another diagnostic laparoscopy was performed revealing a normal appendix. Subsequent laparoscopic appendicectomy was performed which was histopathology confirmed as a normal appendix. His symptoms did not improve after surgery and he developed localised guarding in the right iliac fossa, low grade pyrexia, tachycardia and raised inflammatory markers. An ultrasound scan was performed which was unremarkable. Computed tomography (CT) abdomen revealed a small collection from which extended a thin tubular structure ending in the terminal ileum. A third diagnostic laparoscopy was performed. The small collection was not identified and conversion to midline laparotomy revealed a second necrotic friable appendix leading to a retrocaecal and retroileal cavity (abscess). This was confirmed on histopathology to be a gangrenous appendix with secondary peritonitis. He was discharged from hospital several days post-operatively. A year later he represented to our services with an incisional hernia which was repaired laparoscopically.

Conclusions

Dual appendix is a well described but rare congenital abnormality that is well described by the Cave-Wellbridge classification. This congenital abnormality is often recognised incidentally at surgery or on post-mortem examination. Radiological studies are often not useful aids in making the diagnosis of duplicate appendix. Hence the possibility of a duplex appendix should be considered and sought during diagnostic laparoscopy performed in patients presenting with recurrent right iliac fossa symptoms.

病例报告:一例罕见的右侧髂窝疼痛
双阑尾是一种罕见的先天性畸形,发病率为5万分之2。双侧阑尾炎是一种罕见但公认的现象。这种先天性异常的不寻常表现可能导致诊断和治疗的延误。病例描述:42岁男性,右髂窝疼痛2天,炎症标志物升高。他接受了诊断性腹腔镜检查,发现阑尾正常。未行腹腔镜阑尾切除术。几年后,他出现了类似的症状,再次进行腹腔镜检查,发现阑尾正常。随后进行腹腔镜阑尾切除术,组织病理学证实为正常阑尾。手术后症状没有改善,出现右髂窝局部守卫、低度发热、心动过速和炎症标志物升高。进行了超声扫描,没有什么异常。腹部计算机断层扫描(CT)显示一个小集合,延伸到回肠末端的细管状结构。第三次诊断腹腔镜检查。小的收集没有被识别,转换到中线剖腹术发现第二个坏死易碎的阑尾,导致盲肠后和回肠后腔(脓肿)。组织病理学证实为坏疽性阑尾伴继发性腹膜炎。手术后几天他出院了。一年后,他代表我们的服务切口疝是腹腔镜修复。结论双阑尾是一种罕见的先天性畸形,适用于Cave-Wellbridge分类。这种先天性异常通常在手术或尸检时偶然发现。在诊断重复阑尾时,放射学检查往往不能起到辅助作用。因此,在出现复发性右髂窝症状的患者进行诊断性腹腔镜检查时,应考虑并寻求双阑尾的可能性。
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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