Spinal cord fissure is not a rare spinal cord malformation, which is a bony longitudinal septum inside the vertebral canal that divides the spinal cord into two halves, and some are cartilage or fibrous longitudinal septum, a few cases are double spinal cord (diplomyelia).
The spinal cord is located in the vertebral canal. During the process of human growth and development, the growth rate of the vertebral canal is faster than that of the spinal cord, so the lower end of the spinal cord gradually rises relative to the lower end of the vertebral canal. Spinal cord tethering means that the lower end of the spinal cord is restricted by various reasons at the end of the vertebral canal, so it cannot rise normally, making its position lower than normal. It is one of the main pathological mechanisms caused by various congenital developmental abnormalities leading to neurological symptoms, and the series of clinical manifestations caused by this is called spinal cord tethering syndrome, also known as spinal cord tethering syndrome. Some people believe that the occurrence mechanism of spinal cord fissure is caused by factors other than nerves, that is, the abnormal development of vertebral bones; some people also believe that it is caused by the abnormal development of nerves, followed by the abnormal development of vertebral bones. The spinal cord is divided into left and right, with the hard meningeal tube accompanying the split and non-split types. That is, Type I: double meningeal sac and double spinal cord type, that is, the spinal cord is completely separated by fibrous tissue, cartilage, or bone spurs at the longitudinal fissure, divided into two, each with its own hard meningeal and arachnoid membrane, and the spinal cord is pulled by the separator, causing symptoms. Type II: common meningeal sac and double spinal cord type, the meninges are often separated by fibrous septa at the longitudinal fissure, into two parts, but with a common hard meningeal and arachnoid membrane, generally without clinical symptoms.