Large skull base involvement of rhino-orbital-cerebral mucormycosis with rapidly progressive onset in immunocompetent patient mimicking a sphenoid meningioma.

Surgical neurology international Pub Date : 2025-08-01 eCollection Date: 2025-01-01 DOI:10.25259/SNI_132_2025
Haifaa Mechergui, Sofiene Bouali, Asma Bouhoula, Nesrine Nessib, Khalil Ghedira, Khansa Abderrahmen
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Abstract

Background: Invasive skull base of rhino-orbital-cerebral mucormycosis is rare, rapidly progressive, and potentially life-threatening disease, and it usually occurs in immunocompromised patients. We are witnessing an unprecedented peak of rhino-cerebral mucormycosis since the second wave of the Coronavirus Disease-2019 pandemic.

Case description: A 31-year-old man experienced a sudden onset of decreased visual acuity associated with right exophthalmos and paroxysmal headache that had been ongoing for 2 months before his presentation. On examination, he presented a frontal syndrome with preserved eye movement, with vision impairment, and with bilateral stage 3 papilledema. In addition, the patient is feverish, and the general examination showed no lesion of the nose or skin. All biological investigations were done and were negative, even a COVID-19 test. Brain magnetic resonance imaging revealed a right extra-axial temporal lesion that was isointense on T1-weighted imaging, hypointense on T2-weighted imaging, and well enhancing with gadolinium. The lesion extended into the orbit, cavernous sinus (involving the optic nerve and internal carotid artery), and the infratemporal fossa, suggestive of a sphenoidal meningioma. The patient underwent subtotal resection. Postoperatively, the patient remained feverish, and his condition was worsening. He died 6 days after the surgery. A brain infection was impossible to diagnose until after his death. The anatomopathological examination confirmed mucormycosis.

Conclusion: The findings from the present case indicate that a large intracranial mass is an uncommon clinical characteristic of cerebral mucormycosis in an immunocompetent patient. It can manifest with the classic symptoms of large temporal spheno-orbital invasive meningiomas. To the best of our knowledge, very few studies are reported depicting the patterns of skull base involvement and associated neurological implications of patients with skull base involvement of rhino-orbital-cerebral mucormycosis along with its clinical, radiological, intraoperative, and post-operative correlates.

模拟蝶骨脑膜瘤的免疫功能正常患者的鼻-眶-脑毛霉菌病伴快速进展性发作的大颅底受损伤。
背景:鼻-眶-脑毛霉菌病侵袭颅底是一种罕见的、进展迅速的、潜在威胁生命的疾病,通常发生在免疫功能低下的患者中。自第二波冠状病毒病-2019大流行以来,我们正在目睹前所未有的鼻-脑毛霉菌病高峰。病例描述:一名31岁男子突然出现与右眼突出和阵发性头痛相关的视力下降,在他就诊前已经持续了2个月。检查时,他表现为额叶综合征,眼球运动保留,视力受损,双侧3期乳头水肿。此外,患者发热,全身检查未见鼻及皮肤病变。所有生物调查均为阴性,即使是COVID-19检测也是如此。脑磁共振示右侧颞轴外病变,t1加权等强,t2加权低,钆增强良好。病变扩展到眼眶、海绵窦(累及视神经和颈内动脉)和颞下窝,提示蝶骨脑膜瘤。病人接受了次全切除术。术后患者持续发热,病情不断恶化。他在手术后6天死亡。脑部感染直到他死后才被诊断出来。解剖病理检查证实为毛霉病。结论:本病例的结果表明,在免疫功能正常的患者中,颅内大肿块是脑毛霉菌病的罕见临床特征。它可以表现为典型的颞部-眶部侵袭性脑膜瘤。据我们所知,很少有研究报道描述鼻-眶-脑毛霉菌病颅底受累模式和颅底受累患者的相关神经学影响及其临床、放射学、术中和术后相关因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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