Olfactory Neuroblastoma Presenting as a Submandibular Mass

S. Appukutty, S. Palma, S. Whitaker, K. Wood
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Abstract

Background: Olfactory Neuroblastoma is a rare, locally aggressive malignant neoplasm arising from the olfactory epithelium, which causes metastasis by lymphatic and haematogenous routes, with most common site being the cervical lymph nodes. Materials and Methods: Clinical history was retrieved from discussion in the Head and Neck multidisciplinary team meeting and medical records. Routine macroscopic and microscopic histological examination along with appropriate immunohistochemistry was performed. In addition, we include the review of literature of olfactory neuroblastoma metastatic to different sites. Results: A 75 year old female presented with a left submandibular mass which on biopsy was diagnosed as high grade neuroendocrine carcinoma requiring further investigation for characterising it as primary or metastatic. The histological diagnosis proved difficult and doubtful, till after five months when on follow up investigation a skull base lesion was identified, this on biopsy was confirmed to be an olfactory neuroblastoma. Conclusion: It is important to think laterally and consider metastatic tumours when evaluating neuroendocrine lesions in the submandibular region as this can be the first manifestation.
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嗅觉神经母细胞瘤表现为下颌骨肿块
背景:嗅觉神经母细胞瘤是一种罕见的,局部侵袭性的恶性肿瘤,起源于嗅觉上皮,可通过淋巴和血液途径转移,最常见的部位是颈部淋巴结。材料和方法:从头颈部多学科小组会议的讨论和医疗记录中检索临床病史。常规肉眼、显微镜组织学检查及适当的免疫组织化学检查。此外,我们还回顾了嗅觉神经母细胞瘤转移到不同部位的文献。结果:一名75岁女性,左侧下颌下肿块,活检诊断为高级别神经内分泌癌,需要进一步调查其原发性或转移性特征。组织学诊断是困难和可疑的,直到5个月后,随访调查发现颅底病变,活检证实为嗅觉神经母细胞瘤。结论:在评估颌下区神经内分泌病变时,考虑转移性肿瘤是很重要的,因为这可能是第一个表现。
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