PDF(Pubmed)
Abstract：
The authors describe a case of a male neonate with split notochord syndrome presenting with cervico-thoracic deformity, thoracic neuroenteric cyst, separate abdominal duodenal duplication cyst and concurrent intestinal malrotation. This combination of abnormalities is very rare. When these lesions are suspected, patients must be investigated carefully.This case is presented not only to recount an infrequent combination of structural abnormalities but also to raise awareness of the signs that should point to clinical suspicion and prompt diagnosis.Following surgical excision of the thoracic neuroenteric cyst, the patient has made a good recovery.
摘要：
作者描述了一例男性新生儿的脊索裂开综合征，表现为颈胸畸形，胸神经肠囊肿,单独的腹部十二指肠重复囊肿和并发肠旋转不良。这种异常的组合非常罕见。当怀疑这些病变时，病人必须仔细调查。这种情况不仅是为了叙述不常见的结构异常组合，而且是为了提高对应指出临床怀疑和及时诊断的体征的认识。手术切除胸神经肠囊肿后，病人恢复得很好。
