Olfactory neuroblastoma: literature review and presentation of two clinical cases with different tumour infiltrations and different approaches

Neurocirugia (English Edition) Pub Date : 2025-05-01 Epub Date: 2024-12-12 DOI:10.1016/j.neucie.2024.12.001
Carlos Andres Ferreira , Carlos Eduardo Quevedo , Gina Vanessa Vilardy , Mario Andres Arias
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Abstract

The olfactory neuroblastoma is a rare malignant neoplasm derived from the olfactory neuroepithelium. It can metastasize to cervical lymph node chains and distant organs through hematogenous or lymphatic routes. Two clinical cases are presented: the first, a 56-year-old man with no pathological history, exhibited symptoms evolving over 2 months, characterized by persistent rhinorrhea with frequent epistaxis, ipsilateral proptosis, left hemicranial pain, anosmia, and dysgeusia. Radiological images showed involvement of paranasal sinuses, left orbital cavity, and intracranial region. The second case involved a 46-year-old male with progressive symptoms over more than 1 year, including nasal obstruction, rhinorrhea, self-limited epistaxis, anosmia, weight loss in the last 3 months, and subjective decrease in visual acuity. A protruding mass in the left nasal fossa was observed without intracranial involvement. Both cases were pathologically and immunohistochemically consistent with olfactory neuroblastoma, Hyams grade 2.
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嗅觉神经母细胞瘤:文献回顾及两例不同肿瘤浸润及不同入路的临床表现。
嗅觉神经母细胞瘤是一种罕见的源自嗅觉神经上皮的恶性肿瘤。它可以通过血液或淋巴途径转移到颈部淋巴结链和远处器官。本文报告两例临床病例:第一例为56岁男性,无病理史,症状发展超过2个月,特征为持续性鼻漏伴频繁鼻出血、同侧突出、左半颅疼痛、嗅觉缺失和发音障碍。影像学显示鼻窦、左眶腔及颅内受累。第二例患者为46岁男性,症状进行性超过1年,包括鼻塞、鼻漏、自限性鼻出血、嗅觉丧失、近3个月体重减轻和主观视力下降。左鼻窝一突出肿块,未累及颅内。两例病理和免疫组织化学均符合嗅神经母细胞瘤,Hyams 2级。
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