Seth Raghav, Sinha Anindita, Singla Navneet, Chatterjee Debajyoti
Radiodiagnosis, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Radiodiagnosis, Post Graduate Institute of Medical Education and Research, Chandigarh, India
BMJ Case Rep. 2021 Mar 18;14(3):e235327. doi: 10.1136/bcr-2020-235327.
Klippel-Feil syndrome is an entity presenting with short neck, low hairline and reduced range of motion of cervical spine. Neurenteric cyst is a congenital abnormality, in which mucus-secreting epithelium of the gastrointestinal tract is seen in the spinal axis. The association of a neurenteric cyst with Klippel-Feil syndrome has been reported very rarely. We report the case of a young man, affected by Klippel-Feil syndrome, who presented with bilateral paraplegia. Imaging of the spine revealed features suggestive of cervico-dorsal neurenteric cyst. Subsequently, surgical resection of the cysts was done, which resulted in resolution of the symptoms.
克-费综合征是一种表现为颈部短、发际线低和颈椎活动范围减小的病症。神经肠囊肿是一种先天性异常,在脊柱中可见胃肠道分泌黏液的上皮组织。神经肠囊肿与克-费综合征的关联报道极少。我们报告一例患有克-费综合征的年轻男性病例,该患者出现双侧截瘫。脊柱影像学检查显示有提示颈胸段神经肠囊肿的特征。随后对囊肿进行了手术切除,症状得以缓解。