Jaggi Ramandeep Singh, Premsagar Ishwar Chandra
Department of Neurosurgery, Dr. R.M.L. Hospital, New Delhi, India.
Pediatr Neurosurg. 2007;43(5):424-7. doi: 10.1159/000106397.
Chiari malformations represent various clinical and anatomic processes that entail varying degrees of involvement of the rhombencephalon (hindbrain). The type III Chiari malformation is distinctly rare. Chiari described only one case of his type III deformity, which is indicative of its rarity. We report a case of Chiari malformation type III, a female child who presented to us at the age of 1 month with a swelling at the back of the neck since birth. MRI revealed a Chiari type III malformation with a high cervical meningoencephalocele along with herniation of cerebellar tissue through the bony defect in the posterior elements of the C2 vertebra. At surgery, the meningoencephalocele was excised along with the gliotic cerebellar tissue, and a posterior fossa decompression along with augmentation duraplasty was done. The postoperative period was uneventful. The case and relevant literature is reviewed.
Chiari畸形代表了各种临床和解剖学过程,这些过程涉及不同程度的菱脑(后脑)受累。III型Chiari畸形极为罕见。Chiari仅描述了一例他的III型畸形病例,这表明其罕见性。我们报告一例III型Chiari畸形病例,一名女婴,出生后1个月时因颈部后方肿胀前来就诊。磁共振成像(MRI)显示III型Chiari畸形,伴有高位颈段脑膨出,同时小脑组织通过C2椎体后部结构的骨缺损疝出。手术中,切除了脑膨出以及胶质化的小脑组织,并进行了后颅窝减压及硬脑膜修补术。术后过程顺利。本文对该病例及相关文献进行了综述。