Jehangir Susan, Ninan Pradeep Joseph, Jacob Tarun John, Eapen Anu, Mathai John, Thomas Reju Joseph, Karl Sampath
Department of Pediatric Surgery, Christian Medical College, Vellore, Tamil Nadu, India.
Department of Radiodiagnosis, Christian Medical College, Vellore, Tamil Nadu, India.
J Indian Assoc Pediatr Surg. 2015 Oct-Dec;20(4):174-8. doi: 10.4103/0971-9261.164246.
Enteric duplications (EDs) are rare aberrations of the embryonic gut. This study was undertaken to define the clinical characteristics and management challenges of this unusual entity in the Indian population.
Hospital records of 35 children with 38 ED operated between 2003 and 2014 were analyzed and followed up.
The median age at presentation was 285 days (range 1-day to 16 years) with male preponderance (71%). Small bowel duplications were the most common (44%), and thoracoabdominal duplications were seen in 8% children compared to 2% in the literature. The median duration of symptoms was 18 days (interquartile range [IQR] 3-210 days). Associated anomalies were seen in 49% children with vertebral and spinal anomalies being the most common. Ultrasonogram (US) was done in 83% children and had a sensitivity of 55%. In the presence of a gastrointestinal bleed, Technetium(99m) pertechnetate scintigraphy scan had a positive predictive value of 80%. Thirty-five lesions were completely removed. Mucosectomy was done in two children, and one total colonic duplication was left in situ after providing adequate internal drainage. There was no postoperative mortality. The follow-up was possible in 66% children.
EDs are uncommon and have varied, nonspecific symptoms. Thoracoabdominal duplications are more common in the Indian population. The US is a good screening tool but requires a high index of suspicion where complete excision is not possible; the provision of adequate internal drainage is an acceptable alternative. The long-term prognosis of children with ED depends on the extent of physiological disturbance due to associated anomalies.
肠道重复畸形(EDs)是胚胎肠道罕见的发育异常。本研究旨在明确印度人群中这种特殊疾病的临床特征及管理挑战。
分析并随访了2003年至2014年间接受手术的35例患有38处肠道重复畸形的儿童的医院记录。
就诊时的中位年龄为285天(范围1天至16岁),男性占优势(71%)。小肠重复畸形最为常见(44%),胸腹部重复畸形在8%的儿童中可见,而文献报道为2%。症状的中位持续时间为18天(四分位间距[IQR] 3 - 210天)。49%的儿童存在相关异常,其中脊柱和脊髓异常最为常见。83%的儿童进行了超声检查(US),其敏感性为55%。在存在胃肠道出血的情况下,锝(99m)高锝酸盐闪烁扫描的阳性预测值为80%。35处病变被完全切除。两名儿童进行了黏膜切除术,一处全结肠重复畸形在提供充分的内引流后原位保留。无术后死亡病例。66%的儿童进行了随访。
肠道重复畸形并不常见,症状多样且无特异性。胸腹部重复畸形在印度人群中更为常见。超声是一种良好的筛查工具,但在无法完全切除的情况下需要高度怀疑;提供充分的内引流是一种可接受的替代方法。肠道重复畸形患儿的长期预后取决于相关异常引起的生理紊乱程度。