Menghwani Himanshu, Piplani Rajat, Yhoshu Enono, Jagdish B, Sree Balija Satya
Department of Pediatric Surgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
J Indian Assoc Pediatr Surg. 2023 Jul-Aug;28(4):271-277. doi: 10.4103/jiaps.jiaps_2_23. Epub 2023 Jul 11.
Intestinal malrotation is a congenital anomaly resulting from abnormal or incomplete rotation and fixation of the midgut during embryogenesis. It commonly presents in the neonatal period (75%) with sudden onset bilious vomiting and rarely beyond infancy (<10%).
The aim of the study was to highlight the clinical features, radiological findings, and treatment outcomes of patients with malrotation presenting beyond infancy.
Eleven consecutive cases of delayed presentation of malrotation presented over a period of 5 years (2017-2021). Data were analyzed retrospectively.
Out of the 11 patients, four were female and seven were male. The age of patients ranged from 14 months to 18 years. Patients beyond infancy present usually with diffuse pain abdomen compared to neonates which present with sudden onset bilious vomiting and therefore difficult to diagnose. Five patients had associated abnormalities such as intussusception or nutcracker syndrome or mesenteric cyst or jejunal stricture or mesenteric lymphadenopathy along with malrotation. Patients underwent ultrasonography, upper gastrointestinal contrast study, and contrast-enhanced computed tomography abdomen to confirm the diagnosis. All patients underwent the Ladd procedure with four requiring resection anastomosis and one requiring excision of the mesenteric cyst. Eight out of eleven patients had favorable outcomes, two develop adhesive intestinal obstruction and required re-exploration, and one had persistent complaints of hematochezia.
Malrotation beyond infancy is a rare diagnosis. Malrotation in older children is usually not suspected because of the wide range of symptoms. A high index of suspicion on ultrasound or computed tomography is required to demonstrate the reversal of superior mesenteric artery and superior mesenteric vein position and related conditions. Early intervention and treatment can prevent catastrophic events such as intestinal volvulus and intestinal ischemia in these patients.
肠旋转不良是一种先天性异常,由胚胎发育过程中中肠旋转和固定异常或不完全所致。它通常在新生儿期出现(75%),表现为突发胆汁性呕吐,很少在婴儿期之后出现(<10%)。
本研究的目的是突出婴儿期之后出现的肠旋转不良患者的临床特征、影像学表现和治疗结果。
在5年期间(2017 - 2021年)连续出现11例肠旋转不良延迟就诊病例。对数据进行回顾性分析。
11例患者中,4例为女性,7例为男性。患者年龄从14个月至18岁不等。与表现为突发胆汁性呕吐的新生儿相比,婴儿期之后出现的患者通常表现为全腹弥漫性疼痛,因此难以诊断。5例患者伴有诸如肠套叠、胡桃夹综合征、肠系膜囊肿、空肠狭窄或肠系膜淋巴结病等相关异常以及肠旋转不良。患者接受了超声检查、上消化道造影检查和腹部增强计算机断层扫描以确诊。所有患者均接受了Ladd手术,4例需要切除吻合术,1例需要切除肠系膜囊肿。11例患者中有8例预后良好,2例发生粘连性肠梗阻并需要再次探查,1例持续有便血主诉。
婴儿期之后的肠旋转不良是一种罕见的诊断。由于症状范围广泛,大龄儿童的肠旋转不良通常不易被怀疑。需要高度怀疑超声或计算机断层扫描以显示肠系膜上动脉和肠系膜上静脉位置的反转及相关情况。早期干预和治疗可预防这些患者发生诸如肠扭转和肠缺血等灾难性事件。