Celebi Suleyman, Ozaydin Seyithan, Polat Esra, Basdas Cemile, Alim Elmas Reyhan, Sander Serdar
Department of Pediatric Surgery, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Department of Pediatric Gastroenterology, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
North Clin Istanb. 2018 Sep;5(3):211-215. doi: 10.14744/nci.2017.60590.
The aim of this study was to review the management of pediatric cases of vitelline duct pathology (VDP) detected surgically or incidentally during the neonatal period and the outcomes.
The data of newborns who were symptomatic and underwent VDP resection or who were incidentally diagnosed with VDP at a single institution between 1985 and 2015 were retrospectively analyzed in terms of age, sex, clinical features, treatment, perioperative findings, ectopic tissue pathology, and postoperative follow-up information.
Among the 36 newborns enrolled in this study, 26 were male and 10 were female (2.6:1). The median weight was 2400 g (range: 800-3090 g). In 16 cases (14 males and 2 females; 7:1) the VDP was surgically repaired. Pathological evaluation indicated that 43% (n=7) of the cases had ectopic gastric mucosa. VDP was incidentally discovered in 12 males and 8 females (1.5:1). VDP was removed in 10 cases (50%) and left intact in others. Ectopic gastric mucosa was observed in 10% of the VDP removal cases. Ectopic gastric tissue was more prevalent in the surgical VDP cases than in the incidentally discovered and VDP removal cases (p<0.05). Male predominance was greater in the surgically repaired cases than in the incidentally discovered cases (p<0.05). One patient whose VDP was discovered incidentally was admitted 3 years later with obstruction due to intussusception caused by Meckel's diverticulum, and 1 patient was admitted with rectal bleeding at 11 years of age.
Symptomatic VDP in the newborn demonstrates a significant gender difference. Symptomatic cases are more likely to have ectopic gastric tissue than non-symptomatic cases. Incidentally detected cases without removal should be followed closely for future complications.
本研究旨在回顾新生儿期手术发现或偶然发现的卵黄管病变(VDP)患儿的治疗及预后情况。
回顾性分析1985年至2015年间在某单一机构有症状并接受VDP切除术或偶然诊断为VDP的新生儿数据,内容包括年龄、性别、临床特征、治疗、围手术期发现、异位组织病理及术后随访信息。
本研究纳入的36例新生儿中,男性26例,女性10例(2.6:1)。中位体重为2400 g(范围:800 - 3090 g)。16例(14例男性,2例女性;7:1)VDP接受了手术修复。病理评估显示,43%(n = 7)的病例有异位胃黏膜。12例男性和8例女性(1.5:1)偶然发现VDP。10例(50%)VDP被切除,其他未处理。VDP切除病例中有10%观察到异位胃黏膜。异位胃组织在手术治疗的VDP病例中比偶然发现及VDP切除病例中更常见(p<0.05)。手术修复病例中的男性优势比偶然发现病例更明显(p<0.05)。1例偶然发现VDP的患儿3年后因梅克尔憩室引起的肠套叠梗阻入院,1例患儿11岁时因直肠出血入院。
新生儿期有症状的VDP存在显著性别差异。有症状的病例比无症状病例更易出现异位胃组织。偶然发现未切除的病例应密切随访以防未来出现并发症。