Chiarenza Salvatore Fabio, Conighi Maria Luisa, Bucci Valeria, Bleve Cosimo
Pediatric Surgery Unit, Regional Center of Pediatric Urology and Minimally Invasive Surgery and New Technologies, AULSS 8, S. Bortolo Hospital, 36100 Vicenza, Italy.
Children (Basel). 2025 Apr 17;12(4):517. doi: 10.3390/children12040517.
Congenital duodenal atresia (DA) (Type I) with a fenestrated web can be characterized by a late presentation with a delayed diagnosis. It is even rarer and usually associated with proximal duodenomegaly. Conventional management involves web resection and duodeno-duodeno anastomosis with or without duodenoplasty. We describe our mininvasive surgical strategy and management, detailing the aspects of laparoscopic techniques.
We retrospectively reviewed the medical records of five patients affected by fenestrated duodenal web (DA) with a delayed onset of symptoms and diagnosis who were managed in our Department over a period of 10 years (2013-2023). We analyzed the age of patients at diagnosis, clinical signs and symptoms, associated congenital anomalies, radiological and intraoperative findings, surgical treatment, and outcomes. Diagnostic examinations included ultrasound (US), Upper-Gastrointestinal Study (UGI), and Esophagogastroduodenoscopy (EGDS).
Three boys and two girls, median age of 5.5 months (range 3-11 months), were included in this study. Three underwent previous surgery for long-gap esophageal atresia (EA), two of Type A, and one of Type C, requiring a gastrostomy immediately after birth (delayed esophageal repair for prematurity in Type C) and subsequent delayed primary anastomosis. Major associated anomalies were EA (3), anterior ectopic anus (1), cloaca (1), and Type IV laryngeal web (1). An antenatal diagnostic suspicion of duodenal atresia (obstruction) on ultrasound was described in two patients. UGI suggested a fenestrated duodenal web, visualized at ultrasound in two patients. Duodenal dilation was associated in two cases. The symptoms were feeding difficulties, nonbilious vomiting, upper abdominal distension, and poor growth. All presented with a pre-ampullary obstruction. Endoscopic confirmation was only possible in one patient. The older patient underwent an endoscopic resection of a duodenal web. In the other four, we performed a laparoscopic longitudinal antimesenteric duodenal incision, web resection (excision), and transverse suture (closure was performed) without duodenoplasty. Intraduodenal Indocyanine Green (ICG) visualization (under near-infrared light) was used in the last two cases. No postoperative complications were recorded, with a mean hospital stay of 8 days. A contrast study performed at 4 weeks demonstrated an improved proximal duodenal profile; patients tolerated a full diet and remained symptom-free.
According to our experience with minimally invasive techniques, laparoscopy and endoscopy are effective and safe, supporting web resection for the management of a duodenal web without tapering of the proximal duodenum. They require advanced technical skills. Intraduodenal-ICG injection during laparoscopic treatment of Type 1 DA allows localization of the duodenal web, confirmation of bowel patency (bowel canalization) and the tightness of suture.
伴有有孔隔膜的先天性十二指肠闭锁(DA,I型)的特点可能是发病较晚且诊断延迟。这种情况更为罕见,通常伴有十二指肠近端扩大。传统治疗方法包括隔膜切除以及十二指肠-十二指肠吻合术,可进行或不进行十二指肠成形术。我们描述了我们的微创手术策略和管理方法,详细介绍了腹腔镜技术的各个方面。
我们回顾性分析了10年间(2013 - 2023年)在我科接受治疗的5例有孔十二指肠隔膜(DA)且症状和诊断延迟出现的患者的病历。我们分析了患者的诊断年龄、临床体征和症状、相关先天性异常、影像学和术中发现、手术治疗及结果。诊断检查包括超声(US)、上消化道造影(UGI)和食管胃十二指肠镜检查(EGDS)。
本研究纳入了3名男孩和2名女孩,中位年龄为5.5个月(范围3 - 11个月)。3例患者曾因长段食管闭锁(EA)接受过手术,其中2例为A型,1例为C型,出生后立即需要进行胃造瘘术(C型因早产延迟进行食管修复),随后进行延迟的一期吻合术。主要相关异常包括EA(3例)、前位异位肛门(1例)、泄殖腔(1例)和IV型喉蹼(1例)。2例患者在产前超声检查中怀疑有十二指肠闭锁(梗阻)。UGI提示有孔十二指肠隔膜,2例患者在超声检查中可见。2例患者伴有十二指肠扩张。症状包括喂养困难、非胆汁性呕吐、上腹部腹胀和生长发育不良。所有患者均表现为壶腹前梗阻。仅1例患者通过内镜得到确诊。年龄较大的患者接受了十二指肠隔膜的内镜切除术。在其他4例患者中,我们进行了腹腔镜下十二指肠纵行系膜对侧切口、隔膜切除(切除)和横向缝合(进行关闭),未进行十二指肠成形术。最后2例患者使用了十二指肠内吲哚菁绿(ICG)可视化(近红外光下)。未记录到术后并发症,平均住院时间为8天。4周时进行的造影检查显示十二指肠近端形态改善;患者能够耐受全量饮食且无症状。
根据我们在微创技术方面的经验,腹腔镜检查和内镜检查有效且安全,支持在不使十二指肠近端变细的情况下进行隔膜切除以治疗十二指肠隔膜。它们需要先进的技术技能。在腹腔镜治疗I型DA期间进行十二指肠内ICG注射可实现十二指肠隔膜的定位、确认肠管通畅(肠管再通)以及缝合的紧密性。