Park Byung-Soo, Shin Dong Hoon, Kim Dong-Il, Son Gyung Mo, Kim Hyun Sung
Department of Surgery, Pusan National University Yangsan Hospital, 20 Geumo-ro, Mulgeum-eup, Yangsan, Gyungsangnam-do, 50612, Republic of Korea.
Department of Pathology, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
BMC Surg. 2018 Aug 1;18(1):48. doi: 10.1186/s12893-018-0380-9.
Appendiceal intussusception is very rare condition with an estimated incidence of 0.01%. Therefore, it is likely to be overlooked. In addition, making the diagnosis before or during surgery is very difficult.
A 60-year-old male who was referred to our gastroenterology center with cecal inflammation found during a colonoscopy. An abdominal computed tomography (CT) following endoscopy revealed a 5 × 2.5 × 4 cm mass-like lesion in the cecum around the ileocolic (IC) valve and appendiceal orifice. The main lesion seemed to be an inflammatory mass rather than a malignancy because it appeared to be an extraluminal or extramucosal lesion. Ultrasonography revealed diffuse wall thickening of the cecum around the appendiceal orifice that was suspicious for an inflammatory mass or a benign mass. A diagnosis was uncertain. The differential diagnosis included chronic appendicitis, appendiceal neoplasm such as appendiceal mucocele, low grade appendiceal mucinous neoplasm. The patient underwent a laparoscopic partial cecectomy. In the surgical field, there was a large mass in the appendiceal orifice. The cecum was partially resected, with care taken to preserve the IC valve. Final histopathological analysis of the surgical specimen revealed an appendiceal intussusception without any mucosal lesion of the appendix. Narrowing of the terminal ileum with a small bowel obstruction and stenosis of the IC valve occurred postoperatively. Therefore, ileocecectomy was performed via a laparoscopic approach. The patient was discharged 11 days after the second surgery without another significant postoperative complication.
We report a rare case of appendiceal intussusception that required reoperation due to ileocolic valve stenosis. If the correct diagnosis of appendiceal intussusception is made, we can select an appropriate surgical treatment based on the classification of appendiceal intussusceptions.
阑尾套叠是一种非常罕见的疾病,估计发病率为0.01%。因此,它很可能被忽视。此外,在手术前或手术中做出诊断非常困难。
一名60岁男性因结肠镜检查时发现盲肠炎症被转诊至我们的胃肠病中心。内镜检查后的腹部计算机断层扫描(CT)显示,在回盲(IC)瓣和阑尾开口周围的盲肠中有一个5×2.5×4 cm的肿块样病变。主要病变似乎是炎性肿块而非恶性肿瘤,因为它似乎是腔外或黏膜外病变。超声检查显示阑尾开口周围的盲肠壁弥漫性增厚,怀疑为炎性肿块或良性肿块。诊断不明确。鉴别诊断包括慢性阑尾炎、阑尾肿瘤,如阑尾黏液囊肿、低级别阑尾黏液性肿瘤。患者接受了腹腔镜部分盲肠切除术。在手术视野中,阑尾开口处有一个大肿块。部分切除盲肠,小心保留IC瓣。手术标本的最终组织病理学分析显示为阑尾套叠,阑尾无任何黏膜病变。术后发生了回肠末端狭窄伴小肠梗阻和IC瓣狭窄。因此,通过腹腔镜手术进行了回盲部切除术。患者在第二次手术后11天出院,没有出现其他严重的术后并发症。
我们报告了一例罕见的阑尾套叠病例,该病例因回结肠瓣狭窄需要再次手术。如果能正确诊断阑尾套叠,我们可以根据阑尾套叠的分类选择合适的手术治疗方法。