Spinal cord embolism syndrome occurs in children or adolescents, mostly due to urinary dysfunction, and is often seen in urology; it affects the school life of the affected children, and many of them miss school and stay away from society. In fact, it is a neurological disease. The spinal cord is located in the spinal canal, and it is generally believed that the spinal column grows faster than the spinal cord during the growth and development of children. If the spinal cord cone is pulled by various factors during the ascending process, making the cone position lower than the normal level, the spinal cord cone and cauda equina will be damaged and produce a series of neurological dysfunction and limb deformity, because the spinal cord cone and cauda equina are fixed by the pull, so the image is called spinal cord The spinal cord is called “embolism” syndrome. The clinical manifestations of spinal cord embolism syndrome are often six major symptoms: 1, pain: usually the lumbosacral pain is more common than the lower extremities, pain is limited to the low back, groin, perineum and buttocks, sometimes can be radiated to the lower extremities, lumbosacral activities, especially flexion and extension movements will make these symptoms increased. 2.Sensory-motor disorders: lower limb motor disorders, manifested as progressive lower limb weakness and walking difficulties; sensory disorders, manifested as numbness and hypoesthesia in the saddle area, i.e. sacrococcygeal area. 3, urinary symptoms: manifested as tension, filling incontinence, frequent urination, increased residual urine and cause recurrent urinary tract infections. 4, rectal dysfunction: weakened peristaltic function of the colon and rectum, loss of normal defecation reflex; manifested as constipation, defecation difficulties. 5, limb deformities: common spinal deformities include scoliosis and excessive anterior convexity of the spine; lower limb deformities, hammertoe, high arched foot, horseshoe foot, foot entropion are seen. 6, lumbosacral skin abnormalities: patients often have local skin depression, hair clumping, subcutaneous lipoma, pigmentation and cutaneous hemangioma, neurotrophic ulcers are rare, etc. Surgical treatment of spina bifida: dominant spina bifida, all require surgical treatment, the timing of surgery is 1-3 months after birth. Simple spina bifida, or other types with mild neurological symptoms, should be operated as early as possible. If surgery is postponed for reasons such as systemic conditions, local protection should be provided, especially for those with exposed spinal cord, to prevent infection. The principle of surgery is to divide and release the surrounding adhesions, incorporate the posteriorly protruding spinal cord or nerve roots back into the spinal canal, remove the excess dural sac, close the spinal opening with tight sutures, repair the fascial overlap on both sides of the fissure, and repair the defect in the vertebral plate (bone graft, etc.). In patients with spinal cord embolism syndrome, spinal canal exploration, release of adhesions and severance of the end filaments are feasible. Strengthen skin care: The skin of the child has a thin stratum corneum and is prone to abrasion leading to bacterial skin infection; on the other hand, because the barrier function of the skin of the child is fragile, and the skin contains more water and has a higher pH value, which is conducive to the growth of pathogenic bacteria, skin care of the child should be strengthened by turning the child every l to 2 hours, turning gently, avoiding dragging, etc., and paying attention to keeping the bed unit clean and tidy, without folds and wrinkles, Give massage to the protruding bone parts after each turn, pay attention to axial turning when turning, and avoid excessive distortion of the torso.