Sekioka Akinori, Fukumoto Koji, Miyake Hiromu, Nakaya Kengo, Nomura Akiyoshi, Yamada Yutaka, Yamada Susumu, Urushihara Naoto
Department of Pediatric Surgery, Shizuoka Children's Hospital, 860 Urushiyama, Aoi-ku, Shizuoka, Shizuoka, 420-8660, Japan.
Pediatr Surg Int. 2019 Oct;35(10):1115-1121. doi: 10.1007/s00383-019-04534-w. Epub 2019 Aug 7.
Intestinal aganglionosis (IA) is so rare that the entity remains unclear. The aim of the present study was to compare the outcomes of patients with IA and those with total colonic aganglionosis (TCA).
The hospital records were retrospectively reviewed from 1977 to 2018. Outcomes were analyzed for the IA group and the TCA group, including clinical presentation, initial management, and operative details.
There were six patients were managed in IA (all male) and seven patients in TCA (4 male). The median age at the first operation was significantly younger in IA than TCA (2 days vs 24 days, p = 0.01). The gap between the intraoperative caliber change (CC) of the intestine and the initial stoma location was not significantly different (7.5 cm vs 12 cm, p = 0.61), but the rate of stoma dysfunction was significantly higher in IA (83% vs 0%, p = 0.005). The gap between the CC and the ganglionated bowel was significantly longer in IA (85 cm vs 10 cm, p = 0.003).
Patients with IA appear to have a high risk for stoma dysfunction after the first operation because of the unexpected gap between the CC and normoganglia. The initial location of the stoma requires careful consideration.
肠神经节缺如(IA)极为罕见,其本质尚不清楚。本研究旨在比较IA患者与全结肠神经节缺如(TCA)患者的治疗结果。
对1977年至2018年的医院记录进行回顾性分析。分析IA组和TCA组的治疗结果,包括临床表现、初始治疗及手术细节。
IA组有6例患者(均为男性)接受治疗,TCA组有7例患者(4例男性)。IA组首次手术时的中位年龄显著低于TCA组(2天对24天,p = 0.01)。肠管术中管径变化(CC)与初始造口位置之间的差距无显著差异(7.5 cm对12 cm,p = 0.61),但IA组造口功能障碍发生率显著更高(83%对0%,p = 0.005)。IA组CC与有神经节肠段之间的差距显著更长(85 cm对10 cm,p = 0.003)。
由于CC与正常神经节之间存在意外差距,IA患者首次手术后似乎有较高的造口功能障碍风险。造口的初始位置需要仔细考虑。