Filho F L, Tatagiba M, Carvalho G A, Weichhold W, Klekamp J, Samii M
Department of Neurosurgery, Nordstadt Hospital, Hannover, Germany.
J Neurosurg. 2001 Jan;94(1 Suppl):129-32. doi: 10.3171/spi.2001.94.1.0129.
Neurenteric cysts of the craniocervical junction (CCJ) are very rare lesions. Their origin is the subject of long-standing controversy, but a failure during the embryogenic phase may be responsible for their formation. Accurate histopathological diagnosis may be difficult due to the similarity they share with other cystic lesions such as colloidal cysts, Rathke cysts, and cystic teratomas. Surgical removal is the treatment of choice for intracranial neurenteric cysts, but in some cases, infiltration of the surrounding structures may hinder complete resection. Three cases of neurenteric cysts located at the CCJ are reported.
颅颈交界区（CCJ）的神经肠囊肿是非常罕见的病变。其起源长期以来一直存在争议，但胚胎发育阶段的失败可能是其形成的原因。由于它们与其他囊性病变如胶样囊肿、拉克囊肿和囊性畸胎瘤相似，准确的组织病理学诊断可能很困难。手术切除是颅内神经肠囊肿的首选治疗方法，但在某些情况下，周围结构的浸润可能会阻碍完全切除。本文报道了3例位于CCJ的神经肠囊肿病例。
