Thurston S E, Lenn N J
Clin Pediatr (Phila). 1984 Nov;23(11):652-4. doi: 10.1177/000992288402301111.
Severe cervical radiculopathy occurred in a child with gastroesophageal duplication who had a previously unrecognized vertebral malformation. We review the literature on the association of vertebral and gastroesophageal anomalies and discuss the recent studies in human embryology which detail the relations of notochord to endoderm and neural ectoderm at about 3 weeks of gestation. This case illustrates the opportunity of preventing nerve root or spinal cord compromise due to such vertebral anomalies when the possibility of their association with gastroesophageal duplication is considered.
一名患有胃食管重复畸形的儿童出现了严重的颈神经根病，该儿童之前存在未被识别的椎体畸形。我们回顾了关于椎体与胃食管异常关联的文献，并讨论了人类胚胎学的最新研究，这些研究详细阐述了妊娠约3周时脊索与内胚层和神经外胚层的关系。该病例表明，当考虑到椎体异常与胃食管重复畸形相关的可能性时，有机会预防因此类椎体异常导致的神经根或脊髓受压。
