Case of nasopharyngeal metastases presenting with multiple atypical cranial nerve deficits

Priyal Tiwari, P. Renjen, D. Chaudhari
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Abstract

Jugular foramen syndrome is an uncommon condition with a wide range of possible causes. We present a rare case of Villaret syndrome as an example of jugular foramen syndrome and illustrate a clinical-radiological approach for diagnosing jugular foramen syndrome. The morphological similarities between mesenchymal tumors such as rhabdomyosarcoma and phyllodes seen in our patient make immuno-histochemical (IHC) characterization essential for a definitive diagnosis. Jugular foramen syndromes, including Vernet syndrome, Collet Sicard, Villaret, Tapia, Jackson, and Schmidt, can manifest with multiple cranial nerve deficits in contiguous areas. In our case, the patient exhibited palate paralysis, pharyngeal anesthesia, and Horner's syndrome, thereby highlighting the differential diagnoses of Villaret syndrome and Tapia syndrome.
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鼻咽癌转移伴多发性非典型颅神经损伤病例
颈静脉孔综合征是一种不常见的疾病,可能的病因多种多样。我们将一例罕见的 Villaret 综合征病例作为颈静脉孔综合征的例子,并说明了诊断颈静脉孔综合征的临床-放射学方法。我们的患者所见的间叶肿瘤(如横纹肌肉瘤和鳞状细胞瘤)形态相似,因此免疫组织化学(IHC)定性对于明确诊断至关重要。颈静脉孔综合征,包括 Vernet 综合征、Collet Sicard 综合征、Villaret 综合征、Tapia 综合征、Jackson 综合征和 Schmidt 综合征,可表现为多个颅神经连续区域的功能障碍。在我们的病例中,患者表现为上腭麻痹、咽部麻醉和霍纳综合征,从而突出了维拉雷特综合征和塔皮亚综合征的鉴别诊断。
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