Makary Raafat, Wolfson David, Dasilva Victor, Mohammadi Amir, Shuja Sania
Department of Pathology, University of Florida Health Science Center, Jacksonville, Florida 32209, USA.
J Neurosurg Spine. 2007 Jun;6(6):579-84. doi: 10.3171/spi.2007.6.6.12.
There is a well-recognized association between dysontogenetic tumors of the spinal cord (including teratomas and enterogenous cysts) and dysraphic congenital spinal malformations. The authors present a case of an adult with an intramedullary mature teratoma (IMMT) at the level of C1-2 of the cord associated with dysraphic congenital spinal malformations. Intramedullary mature teratomas of the cervical region of the spinal cord are very rare in adults; only four such lesions have been reported, two of which involved upper cervical segments. Despite the potentially critical location of the tumor, monitored microsurgery resulted in complete removal of the tumor with an intact surrounding capsule, associated fibrous tract, and ellipse of skin with a central dimple. There was an excellent postoperative neurological outcome. The clinical features, imaging studies, treatment options, postoperative outcome, and plausible pathological correlations of IMMTs are discussed.
脊髓发育异常性肿瘤(包括畸胎瘤和肠源性囊肿)与先天性脊柱裂畸形之间存在一种广为人知的关联。作者报告了一例成年患者,其脊髓C1 - 2水平存在髓内成熟畸胎瘤(IMMT),并伴有先天性脊柱裂畸形。脊髓颈段的髓内成熟畸胎瘤在成年人中非常罕见;仅报告过4例此类病变,其中2例累及上颈段。尽管肿瘤位置可能很关键,但通过监测显微手术成功完整切除了肿瘤,保留了周围完整的包膜、相关纤维束以及带有中央凹陷的椭圆形皮肤。术后神经功能恢复良好。本文讨论了IMMT的临床特征、影像学研究、治疗选择、术后结果以及合理的病理相关性。