Auditory neuroma is one of the common intracranial tumors, accounting for about 7-12% of intracranial tumors. It is a benign tumor that originates from the auditory nerve sheath and can often be cured permanently if completely removed. Patients with auditory neuroma mainly have tinnitus as the first symptom, and progressive hearing loss to deafness on one side. If the tumor involves the cerebellum and brainstem, it may cause unstable walking and ataxia of limb movement. If the tumor continues to develop, it may cause difficulty in swallowing, choking and coughing, and hoarseness of voice. If cerebrospinal fluid circulation is obstructed, cranial hypertension symptoms such as headache, vomiting, and optic papillar edema may occur. The most effective treatment modality for this disease is surgical resection. It is insensitive to radiation and should be removed surgically. The surgical pathway can be taken either through the anterior nostril, through a lateral nasal incision, or through an extra-nasal and septal sinus approach or Corlu surgical resection. Midface decortication has the advantages of wide field and no postoperative facial scars, and is the best procedure to remove neurofibroma in the nasal and sinus areas.