Robot-Assisted Laparoscopic Endorectal Pull-Through Combined with Deloyers Turnover in Long-Segment Hirschsprung Disease: A Case Report.

IF 0.7 Q4 SURGERY
European Journal of Pediatric Surgery Reports Pub Date : 2025-07-11 eCollection Date: 2025-01-01 DOI:10.1055/a-2640-4118
Maria Stella Cipriani, Maria G Faticato, Federica Fanti, Michela C Y Wong, Girolamo Mattioli
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Abstract

We report the first documented pediatric case of the Deloyers procedure performed using robotic surgery to treat a female patient with long-segment Hirschsprung disease. A 9-month-old child was diagnosed with long-segment Hirschsprung disease. Despite rectal irrigations, the patient experienced refractory constipation and enterocolitis, necessitating exploratory surgery and ileostomy. A transition zone was identified at the proximal transverse colon, with mapping biopsies confirming aganglionosis up to the splenic flexure. At 16 months of age, the child underwent a robot-assisted endorectal pull-through with ileostomy closure. Four 8-mm trocars were placed in the epigastric, left subcostal, right subcostal, and right flank regions. Dissection and mobilization extended distally beyond the peritoneal reflection and proximally to the hepatic flexure, preserving the marginal vascular arcades. The middle and right colic arteries were ligated, while the ileocolic artery was preserved. Indocyanine green fluorescence imaging confirmed adequate vascularization of the hepatic flexure. A counterclockwise 180-degree rotation of the right colon was performed. In the perineal phase, a mucosal incision above the dentate line was followed by progressive mucosectomy to reach the isolated rectum. The colon was pulled through, and a tension-free coloanal anastomosis was performed. The postoperative period was uneventful at the 6-month follow-up. Robot-assisted laparoscopic endorectal pull-through with the Deloyers procedure is a feasible and safe technique for long-segment Hirschsprung disease. Larger case series are required to assess its long-term outcomes and potential advantages. An explanatory video of the surgery is available.

机器人辅助的腹腔镜直肠内拔通术联合移位术治疗长段先天性巨结肠1例。
我们报告了第一个记录的儿科病例,使用机器人手术进行Deloyers程序来治疗女性长节段先天性巨结肠疾病。一个9个月大的婴儿被诊断为长节段先天性巨结肠病。尽管进行了直肠冲洗,但患者出现了难治性便秘和小肠结肠炎,需要进行探查性手术和回肠造口术。在近端横结肠处发现一个过渡区,活检证实神经节病直至脾屈曲。在16个月大的时候,孩子接受了机器人辅助的直肠内牵引术和回肠造口术。在腹壁、左肋下、右肋下和右侧区域放置4个8毫米套管针。解剖和活动远端延伸到腹膜反射和近端到肝屈曲,保留了边缘血管拱廊。结扎中、右结肠动脉,保留回结肠动脉。吲哚菁绿荧光成像证实肝屈曲有充分的血管化。右结肠逆时针180度旋转。在会阴期,在齿状线以上的粘膜切口之后进行渐进式粘膜切除术以到达孤立直肠。结肠被拉过,并进行无张力的结肠肛管吻合。术后6个月随访无明显变化。机器人辅助腹腔镜直肠内牵引与Deloyers手术是一种可行和安全的技术,用于长节段巨结肠疾病。需要更大的病例系列来评估其长期结果和潜在优势。该手术的解释性视频可用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
33.30%
发文量
39
审稿时长
12 weeks
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