Tsuchiya D, Kayama T, Kuchiki H, Sato S, Saito S
Department of Neurosurgery, Yamagata University School of Medicine, Japan.
No To Shinkei. 2000 Sep;52(9):811-6.
Olfactory neuroblastoma is a rare tumor originating in the upper nasal cavity. It rarely extends intracranially. We report a clinical case of olfactory neuroblastoma with intracranial extension and distant metastasis. A 35-year-old man complained of nasal stuffiness and bleeding, headache and vomiting. Neurological examination showed anosmia and papilledema. MRI showed a huge mass that occupied the right nasal and paranasal cavities, and extended into the right frontal base. The tumor was removed totally and was histologically diagnosed as olfactory neuroblastoma. About two months after surgery, however, MRI demonstrated a rapid recurrence of the tumor in the nasal and paranasal cavities and the frontal lobe. Metastatic lesions were also seen in the right cervical lymph nodes. Chemotherapy was administered using cisplatin and etoposide. The tumor in the frontal lobe shrunk markedly but the other lesion persisted. Whole brain irradiation and local irradiation of the cervical lymph nodes were performed. The tumors became smaller but did not disappear. MRI demonstrated spinal dissemination. Irradiation of the whole spinal cord was performed. The metastatic lesions disappeared. The patient was discharged without neurological deficits, but died of pneumonia 15 months after surgery. Olfactory neuroblastoma is a slow-growing tumor and is highly radiosensitive, but it rarely extends or develops multiple distant metastases and seldom shows a short survival time, as in our case. A review of the literature documented responses in patients treated with a cisplatin-based drug combination. We recommend systemic control using cisplatin-based chemotherapy in addition to irradiation to prevent local recurrence in cases of advanced or metastatic olfactory neuroblastoma.
嗅神经母细胞瘤是一种起源于鼻腔上部的罕见肿瘤。它很少向颅内扩展。我们报告一例伴有颅内扩展和远处转移的嗅神经母细胞瘤临床病例。一名35岁男性主诉鼻塞、鼻出血、头痛和呕吐。神经系统检查显示嗅觉丧失和视乳头水肿。磁共振成像(MRI)显示一个巨大肿块占据右侧鼻腔和鼻窦,并延伸至右侧额叶底部。肿瘤被完全切除,组织学诊断为嗅神经母细胞瘤。然而,术后约两个月,MRI显示鼻腔、鼻窦和额叶肿瘤迅速复发。右侧颈部淋巴结也可见转移灶。使用顺铂和依托泊苷进行化疗。额叶肿瘤明显缩小,但其他病灶持续存在。进行了全脑照射和颈部淋巴结局部照射。肿瘤变小但未消失。MRI显示脊髓播散。进行了全脊髓照射。转移灶消失。患者出院时无神经功能缺损,但术后15个月死于肺炎。嗅神经母细胞瘤是一种生长缓慢的肿瘤,对放疗高度敏感,但很少扩展或发生多处远处转移,很少像我们的病例那样生存期短。文献回顾记录了使用基于顺铂的联合药物治疗患者的反应。对于晚期或转移性嗅神经母细胞瘤病例,我们建议除放疗外,使用基于顺铂的化疗进行全身控制,以预防局部复发。