Intravertebral tumors in children — i.e., spinal cord tumors, generally can be divided into epidural, subdural, and intraspinal according to the location of growth, and there are a few that span the above 2-3 levels, pathologically congenital tumors are the majority, generally benign, but epidural tumors are mostly malignant, and often connected with extravertebral tumors — such as those located in the posterior mediastinum or retroperitoneum. Other congenital tumors often combine with some spinal cord deformities, such as spina bifida, scoliosis, kyphosis, spinal cord embolism, spondylolisthesis, spinal longitudinal bifida, etc. Spinal cord tumors often cause compression of the spinal cord and nerves, resulting in physical and bowel movement disorders. MRI is the best diagnostic tool. Surgery should be performed as soon as the diagnosis is clear, and the tumor should be removed as much as possible to protect the spinal cord, and the combined spinal deformity should be treated. The effect after surgery depends on the nature of tumor growth, damage to the spinal cord spine, pre-surgical symptoms, surgical procedure and tumor pathology. Children’s body has a great ability to recover, so they should not give up easily in treatment.