Nasif Hamza Abdulkarim, Salloum Omar H, Al-Atrash Sundus Imran, Makhlouf Taha Z, Al-Fallah Orwa, Salhab Rafiq
Faculty of Medicine, Palestine Polytechnic University, Wadi Al-Hariyah Street, Hebron 9020000, Palestine.
General Surgery Department, Al-Ahli Hospital, Hebron 9020000, Palestine.
J Surg Case Rep. 2025 May 7;2025(5):rjaf282. doi: 10.1093/jscr/rjaf282. eCollection 2025 May.
Appendiceal intussusception is an exceedingly rare condition where a segment of the appendix invaginates into itself or the cecum. We present a case of a 22-year-old female without significant medical history who presented to the emergency room with acute abdominal pain, nausea, vomiting, and fever for 7 hours. Clinical examination revealed diffuse abdominal tenderness and guarding, with stable vitals. Laboratory results showed leukocytosis and elevated C-reactive protein. Abdominal ultrasound and a limited non-contrast computed tomography scan, suggested ileocecal intussusception, but the appendix was not visualized, indicating it as the leading point. Intraoperatively, an inflamed appendix with mucocele and a Type IV intussusception, where the appendix telescoped into itself and the cecum, was found. Manual reduction, appendectomy, and partial cecectomy were performed. Histopathology confirmed severe appendiceal inflammation but no malignancy. This case highlights the diagnostic challenges and rarity of Type IV appendiceal intussusception, emphasizing the importance of surgical exploration in complex presentations.
阑尾套叠是一种极其罕见的病症,即阑尾的一段套入其自身或盲肠。我们报告一例22岁女性病例,该患者无重大病史,因急性腹痛、恶心、呕吐和发热7小时就诊于急诊室。临床检查发现全腹压痛及肌紧张,生命体征稳定。实验室检查结果显示白细胞增多及C反应蛋白升高。腹部超声和有限的非增强计算机断层扫描提示回盲部套叠,但未发现阑尾,提示阑尾为套叠起始点。术中发现阑尾发炎并伴有黏液囊肿,以及IV型套叠,即阑尾套入其自身及盲肠。进行了手法复位、阑尾切除术和部分盲肠切除术。组织病理学证实阑尾有严重炎症,但无恶性病变。该病例突出了IV型阑尾套叠的诊断挑战及罕见性,强调了在复杂临床表现中进行手术探查的重要性。