Ejaz Tallat, Saad Eltaib, Nabil Andik, Slattery James
Department of Surgery, Midland Regional Hospital Mullingar, Longford Road, Mullingar, Co-Westmeath, Ireland.
Department of Radiology, Midland Regional Hospital Mullingar, Longford Road, Mullingar, Co-Westmeath, Ireland.
Case Rep Surg. 2019 Jan 15;2019:6508642. doi: 10.1155/2019/6508642. eCollection 2019.
A 46-year-old female presented to our emergency department (ED) with a 2-day history of right lower abdominal pain which was associated with nausea and anorexia. Abdominal examination revealed tenderness in the right iliac fossa (RIF) with rebound tenderness and a localized guarding. Urine dipstick was normal, and the pregnancy test was negative. Her laboratory investigations were significant only for a CRP of 16.6. A presumptive clinical diagnosis of acute appendicitis was suggested based on the given history and relevant physical signs. However, an abdominal computed tomography (CT) scan revealed an epiploic appendagitis of the caecum with a normal-looking appendix. She was managed conservatively and responded well and was discharged after 2 days in good health. Though being a relatively rare case of acute localized right-sided lower abdominal pain, caecal epiploic appendagitis should be considered as one of the differential diagnoses with the final diagnosis reached usually by the radiological findings due to the nonspecific nature of clinical and laboratory features.
一名46岁女性因右下腹痛2天前来我院急诊科就诊,伴有恶心和厌食。腹部检查发现右髂窝压痛,有反跳痛和局限性肌紧张。尿试纸检查正常,妊娠试验阴性。她的实验室检查仅C反应蛋白为16.6有意义。根据所给病史和相关体征,初步临床诊断为急性阑尾炎。然而,腹部计算机断层扫描(CT)显示盲肠的网膜附件炎,阑尾外观正常。她接受了保守治疗,反应良好,2天后健康出院。尽管盲肠网膜附件炎是急性局限性右下腹痛的相对罕见病例,但由于临床和实验室特征的非特异性,应将其视为鉴别诊断之一,最终诊断通常通过影像学检查得出。