Nasopharyngeal Giant Carcinoma Mimicking Intracranial Lesions: A Case Report and Literature Review.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Ying Zilan, Zhimin Ye
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引用次数: 0

Abstract

BACKGROUND Nasopharyngeal carcinoma can directly invade the intracranial cavity through skull base foramina in advanced-stage patients. Due to both the multiple cranial nerve injuries associated with nasopharyngeal base invasion and the proximity of the pituitary gland, it is challenging to differentiate this condition from intracranial space-occupying lesions, such as meningiomas and pituitary adenomas, in the early stages. This report describes a 37-year-old woman with bilateral nasal congestion, diplopia, hearing loss, and headache diagnosed with a large nasopharyngeal carcinoma invading the cerebellum, pons, medulla oblongata, and cervical spinal cord. CASE REPORT A 37-year-old woman with nasopharyngeal carcinoma (NPC) exhibiting extensive intracranial invasion - involving the mesencephalon, cerebellum, pons, medulla oblongata, and cervical spinal cord - was, with difficulty, diagnosed as having intracranial space-occupying lesions (meningiomas/pituitary tumors) by some renowned neurosurgical centers. She came to our hospital using a wheelchair, exhibiting vague pronunciation, decreased bilateral hearing, headache, facial numbness, diplopia, and coughing when drinking water. Following definitive diagnosis through nasopharyngeal biopsy confirming non-keratinizing carcinoma, we quickly proceeded with treatment. After receiving 6 cycles of chemotherapy with anti-PD-1 immunotherapy, followed by tomotherapy with concurrent nivolumab, the lesion was dynamically reduced, and efficacy was assessed as a complete response (CR). Therapy significantly improved her symptoms, with the holocranial headache resolving, intelligible speech restored, and facial sensation recovered. CONCLUSIONS This case highlights the importance of routinely integrating nasopharyngeal MRI and biopsy when evaluating patients with atypical cranial neuropathies. Furthermore, multidisciplinary team (MDT) collaboration is essential to avoid delayed diagnosis in NPC cases with extensive skull base invasion.

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鼻咽癌模拟颅内病变:1例报告及文献复习。
背景鼻咽癌晚期患者可经颅底孔直接侵及颅腔。由于侵犯鼻咽基底的多发性颅神经损伤和邻近垂体,在早期将这种情况与颅内占位性病变(如脑膜瘤和垂体腺瘤)区分是具有挑战性的。本报告报告一位37岁女性,双侧鼻塞、复视、听力丧失和头痛,诊断为大面积鼻咽癌侵犯小脑、脑桥、延髓和颈脊髓。病例报告:一名37岁鼻咽癌(NPC)女性患者表现出广泛的颅内侵犯,累及中脑、小脑、脑桥、延髓和颈脊髓,在一些著名的神经外科中心被诊断为颅内占位性病变(脑膜瘤/垂体瘤)。她是坐轮椅来我院的,表现为发音不清,双侧听力下降,头痛,面部麻木,复视,喝水时咳嗽。通过鼻咽活检确诊非角化癌后,我们迅速进行治疗。在接受6个周期的抗pd -1免疫治疗化疗后,同时进行纳武单抗的断层治疗,病变动态缩小,疗效评估为完全缓解(CR)。治疗显著改善了她的症状,颅头痛消退,语言恢复,面部感觉恢复。结论:本病例强调了在评估非典型颅神经病变患者时,常规整合鼻咽MRI和活检的重要性。此外,多学科团队(MDT)合作是必要的,以避免延误诊断的鼻咽癌病例广泛颅底侵犯。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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