Rustamzadeh Edward, Graupman Patrick C, Lam Cornelius H
Department of Neurosurgery, University of Minnesota, Minneapolis, Minnesota 55455, USA.
J Neurosurg. 2006 May;104(5 Suppl):362-5. doi: 10.3171/ped.2006.104.5.362.
Basicranial diastematomyelia is an extremely rare congenital disorder. A review of the literature indicates only one reported case of basicranial diastematomyelia in which an osseous peg divided the brainstem in two. The authors present the first reported case of basicranial diplomyelia split by a fibrous band and correlate its pathogenesis with that of split cord malformation (SCM). The patient described in the present report had a fibrous stalk dividing the brainstem, and therefore the condition was categorized as a diplomyelia, or SCM Type II. Because the occipital dermatomes behave similarly to the spinal dermatomes early in development, they may be subject to the same embryonic error that results in SCM. The authors propose that the mechanism leading to SCM is the same as that found in basicranial split malformations and that the theory explaining it be modified to include the posterior fossa.
颅底脊髓纵裂是一种极其罕见的先天性疾病。文献综述表明,仅有一例关于颅底脊髓纵裂的报道,其中一个骨栓将脑干一分为二。作者报告了首例由纤维带分隔的颅底脊髓纵裂病例,并将其发病机制与脊髓纵裂畸形(SCM)的发病机制相关联。本报告中描述的患者有一个纤维束将脑干分开,因此该病症被归类为脊髓纵裂,即SCM II型。由于枕部皮节在发育早期的表现与脊髓皮节相似,它们可能会受到导致SCM的相同胚胎发育错误的影响。作者提出,导致SCM的机制与颅底分裂畸形中发现的机制相同,并且解释该机制的理论应加以修改,以纳入后颅窝。