Kalfoutzou Areti, Restemi Asimina, Rapti Cleopatra, Chaleplidis Nikolaos, Bagiokou Eleftheria, Bartzi Dimitra, Ramfidis Vasileios
Department of Medical Oncology, 251 Air Force General Hospital, Athens, GRC.
Department of Pathology, 251 Air Force General Hospital, Athens, GRC.
Cureus. 2024 Nov 6;16(11):e73105. doi: 10.7759/cureus.73105. eCollection 2024 Nov.
Olfactory neuroblastoma is an extremely rare malignancy of the sinonasal tract. It is a neuroectodermal tumor, originating from the olfactory epithelium of the nasal and sinus cavities. Due to its rarity, no standard of care treatments have been established to date. We present a case involving a young adult who presented for evaluation of a palpable cervical lymph node. Nasal endoscopy and Magnetic Resonance Imaging (MRI) of the visceral cranium showed a space-occupying lesion in the right nasal cavity, along with a suspicious right submandibular lymph node block. Fine Needle Biopsy (FNB) of the cervical lymph node was suggestive of a small round blue cell tumor, confirming the diagnosis of olfactory neuroblastoma. Staging Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography (FDG-PET/CT) scan identified multiple bone-lytic metastases. The patient was treated with three lines of systemic therapy, but unfortunately, he succumbed to his disease. This case aims to highlight the intricacies of diagnosing and treating one of the rarest malignancies of the head and neck, particularly in the metastatic setting.
嗅神经母细胞瘤是一种极其罕见的鼻窦恶性肿瘤。它是一种神经外胚层肿瘤,起源于鼻腔和鼻窦的嗅上皮。由于其罕见性,迄今为止尚未确立标准的治疗方案。我们报告一例年轻成人病例,该患者因可触及的颈部淋巴结前来评估。鼻腔内窥镜检查和头颅磁共振成像(MRI)显示右侧鼻腔有占位性病变,同时伴有可疑的右侧下颌下淋巴结肿大。颈部淋巴结细针穿刺活检(FNB)提示为小圆蓝细胞瘤,确诊为嗅神经母细胞瘤。分期氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG-PET/CT)显示多处溶骨性转移。该患者接受了三线全身治疗,但不幸的是,最终死于该疾病。本病例旨在强调诊断和治疗头颈部最罕见的恶性肿瘤之一的复杂性,尤其是在转移情况下。