Samuk Inbal, Nica Adriana, Lakovski Yaniv, Freud Enrique
Department of Pediatric Surgery, Schneider Children's Medical Center of Israel, Sackler Faculty of Medicine, Tel Aviv University, Petah Tikva, Israel.
Department of Radiology, Schneider Children's Medical Center of Israel, Sackler Faculty of Medicine, Tel Aviv University, Petah Tikva, Israel.
Eur J Pediatr Surg. 2018 Feb;28(1):30-33. doi: 10.1055/s-0037-1604400. Epub 2017 Jul 25.
Appendiceal intussusception is a rare condition in children characterized by an invagination of the appendix into the cecum to various degrees. The treatment is appendectomy; however since symptoms are not specific, clinical diagnosis is challenging and frequently only intraoperative. We present a series of five patients with appendiceal intussusception and discuss features that may direct the pediatric surgeon to achieve early recognition and provide optimal treatment.
The database of a tertiary medical center was retrospectively reviewed for all patients treated for appendiceal intussusception during the period from January 1995 to January 2016. Data collected by chart review included demographics, clinical characteristics, imaging studies, surgical technique, and outcome. The findings were analyzed by descriptive statistics.
This series included five patients (two females and three males) with ages ranging between 27 and 42 months (mean: 35.2). Patients presented with intermittent abdominal pain (IAP, all five patients), alternate vomiting (three of five patients), alternate diarrhea (two of five patients), fever (two of five patients), and rectal bleeding (one of five patients). The average length of symptoms was 22.6 days. Eighteen diagnostic studies were performed, including abdominal ultrasound for all patients, barium enema for three patients with secondary ileocolic intussusception, and abdominal computed tomography (CT) for one patient. The average number of studies per patient was 3.6. In surgery, the appendiceal intussusception was found to be complete in four patients, whereas it was partial in the remaining patient. In all patients, appendectomy was performed with resection of a small rim of cecal wall due to marked congestion and edema in an attempt to decrease recurrence.
The mainstay of clinical presentation is intermittent abdominal pain while patients may be completely asymptomatic between attacks. Appendiceal intussusception may act as a leading point to ileocolic intussusception and is frequently concealed by it. The treatment is appendectomy. Both pediatric surgeons and radiologists should be aware of this occurrence to provide adequate management and avoid complications.
阑尾套叠是儿童中的一种罕见病症,其特征为阑尾不同程度地套入盲肠。治疗方法为阑尾切除术;然而,由于症状不具特异性,临床诊断具有挑战性,且常常只能在术中确诊。我们报告了一系列五例阑尾套叠患者,并讨论了可能有助于小儿外科医生早期识别并提供最佳治疗的特征。
回顾性分析了一家三级医疗中心1995年1月至2016年1月期间所有接受阑尾套叠治疗患者的数据库。通过病历审查收集的数据包括人口统计学资料、临床特征、影像学检查、手术技术和结果。采用描述性统计方法分析研究结果。
该系列包括五例患者(两名女性和三名男性),年龄在27至42个月之间(平均:35.2个月)。患者表现为间歇性腹痛(所有五例患者)、交替性呕吐(五例患者中的三例)、交替性腹泻(五例患者中的两例)、发热(五例患者中的两例)和直肠出血(五例患者中的一例)。症状的平均持续时间为22.6天。共进行了18项诊断性检查,包括对所有患者进行腹部超声检查、对三例继发性回结肠套叠患者进行钡剂灌肠检查以及对一例患者进行腹部计算机断层扫描(CT)检查。每位患者的检查平均次数为3.6次。手术中发现,四例患者的阑尾套叠为完全性,而其余一例患者为部分性。在所有患者中,均进行了阑尾切除术,并切除了一小圈盲肠壁,原因是盲肠壁明显充血和水肿,以试图降低复发率。
临床表现的主要特征是间歇性腹痛,而患者在发作间歇期可能完全无症状。阑尾套叠可能成为回结肠套叠的起始点,并常常被其掩盖。治疗方法为阑尾切除术。小儿外科医生和放射科医生都应意识到这种情况的发生,以便提供适当的管理并避免并发症。