Ciu S X
PLA General Hospital, Beijing.
Zhonghua Zhong Liu Za Zhi. 1991 Jul;13(4):316-8.
This paper reports 4 patients with pathologically proven olfactory neuroblastoma. This tumor most commonly occurs along the medial line of the nasal cavity, base of the anterior cranial fossa, or the ethmoid sinuses. Special stain or electron-microscopy should be done routinely to ensure diagnostic accuracy if a mass at the above sites was suspected to be an olfactory neuroblastoma. Ample excision and preoperative and/or postoperative radiotherapy was recommended. The irradiation field should be large enough and the dose more than 60 Gy. The prognosis of patients in Group C of Kadish classification and children was poor. Recurrence and metastasis might still occur many years after the initial treatment, necessitating close follow-up.
本文报告了4例经病理证实的嗅神经母细胞瘤患者。该肿瘤最常发生于鼻腔中线、前颅窝底部或筛窦。如果怀疑上述部位的肿物为嗅神经母细胞瘤,应常规进行特殊染色或电子显微镜检查以确保诊断准确性。建议充分切除并进行术前和/或术后放疗。照射野应足够大,剂量应超过60 Gy。卡迪什分类C组患者及儿童的预后较差。初始治疗多年后仍可能发生复发和转移,需要密切随访。