有症状的儿童脐肠管异常。

IF 0.4 4区 医学 Q4 SURGERY South African Journal of Surgery Pub Date : 2024-10-01
G Gerçel, A I Anadolulu
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引用次数: 0

摘要

背景:我们的目的是介绍我们对有症状的肠管(OMD)异常患儿的治疗经验,并评估患者的特征、治疗和结果:回顾性分析了2018年10月至2022年11月期间在桑尼乌尔法培训与研究医院接受手术治疗的无症状OMD异常儿童的记录:35名患者的中位年龄为31.7周(1天-17岁),其中29名(82.8%)为男性,6名(17.2%)为女性。17例(48.6%)患者出现胃肠道梗阻,11例(31.4%)出现急腹症,4例(11.4%)出现脐部异常,3例(8.6%)出现直肠出血。所有出现脐部异常的患者都是新生儿。这些脐部异常现象分别是皮肤 OMD 瘘(1 例)、脐带疝囊 OMD 瘘(1 例)、脐带疝 OMD 囊肿(1 例)和脐带疝囊 OMD 带粘连(1 例)。三名直肠出血患者的梅克尔扫描结果均为阳性。除脐部异常外,其他患者的手术结果为憩室炎(有/无穿孔)(14 例)、憩室引起的肠套叠(9 例)和梅克尔带阻塞(8 例)。手术中,19 例患者进行了回肠切除,10 例患者进行了楔形切除,5 例患者用订书机切除,1 例患者进行了回结肠切除。在组织病理学检查中,11 例标本检测到异位胃黏膜,2 例标本检测到胃和胰腺组织。术后并发症只有两例(切口疝,1 例;术后结肠穿孔,1 例),所有患者均存活良好:在本研究中,消化道梗阻是有症状的 OMD 异常患者的主要症状,而脐部异常仅见于新生儿。手术被确认为最终治疗方法,楔形切除术和单纯憩室切除术虽然安全,但有时并不充分。相当一部分患者可能因严重并发症而需要进行更复杂的肠段切除术。约有三分之一的病例会发现异位组织,因此处理 OMD 异常带来了独特的挑战。
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Symptomatic omphalomesenteric duct anomalies in children.

Background: We aimed to present our experience with children with symptomatic omphalomesenteric duct (OMD) anomalies and evaluate the patients' characteristics, treatment, and outcomes.

Methods: Records of children who were operated for symptomatic OMD anomalies in Şanlıurfa Training and Research Hospital between October 2018 and November 2022 were retrospectively analysed.

Results: There were 35 patients with a median age of 31.7 (1 day-17 years) weeks, 29 (82.8%) males and six (17.2%) females. The presenting signs were gastrointestinal tract (GIT) obstruction in 17 (48.6%) patients, acute abdomen in 11 (31.4%), umbilical abnormalities in four (11.4%) and rectal bleeding in three (8.6%). All patients presenting with umbilical abnormalities were newborn. These were OMD fistula to skin (n = 1), OMD fistula to umbilical cord hernia sac (n = 1), OMD cyst in umbilical cord hernia (n = 1) and OMD band adherence to umbilical cord hernia sac (n = 1). Meckel's scan was positive in all three patients with rectal bleeding. Surgical findings in patients other than umbilical abnormalities were diverticulitis (with/without perforation) (n = 14), intussusception due to diverticulum (n = 9) and Meckel's band obstruction (n = 8). At surgery, an ileal resection was performed in 19 cases, wedge resection in 10 cases, resection with stapler in five cases and ileocolonic resection in one patient. On histopathological examination, ectopic gastric mucosa was detected in 11 specimens and both gastric and pancreatic tissue in two. There were only two cases of postoperative complications (incisional hernia, n = 1, postoperative colon perforation due to forced manual reduction of intussusception, n = 1) and all patients survived in good condition.

Conclusion: In the present study, GIT obstruction is the primary symptom in patients with symptomatic OMD anomalies, with umbilical anomalies exclusively found in newborns. Surgery is confirmed as the definitive treatment, with wedge resection and simple diverticulectomy being safe but sometimes insufficient. A significant portion of patients might need more complex segmental bowel resections due to severe complications. With ectopic tissue found in about one-third of cases, managing OMD anomalies presents distinct challenges.

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来源期刊
CiteScore
0.80
自引率
20.00%
发文量
43
审稿时长
>12 weeks
期刊介绍: The South African Journal of Surgery (SAJS) is a quarterly, general surgical journal. It carries research articles and letters, editorials, clinical practice and other surgical articles and personal opinion, South African health-related news, obituaries and general correspondence.
期刊最新文献
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