原发性颞骨脑膜瘤表现为慢性乳突炎及乙状窦血栓形成1例并文献分析

M. Torrez, E. Fischer, Shweta Agarwal
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引用次数: 0

摘要

耳和颞骨的原发性颅外脑膜瘤极为罕见,占所有脑膜瘤的比例不到1%。在组织学上,它们与颅内对应物无法区分。组织病理学诊断通常具有挑战性,对这种不寻常位置的肿瘤的鉴别诊断相当广泛。我们报告一名64岁男性患者,有癫痫病史,表现为合并乳突炎和乙状窦血栓形成。CT和MRI结果提示慢性炎症过程。手术结果包括从乳突窦向后延伸至乙状窦的肉色肿块。要求进行术中会诊,得到有利于鳞状细胞癌的诊断,并决定结束手术。额外的组织被提交进行永久性评估,活检显示1级脑膜瘤,形态学特征和免疫表型支持。讨论了患者的临床和组织学表现,我们强调了这种罕见实体的挑战性,特别是在术中分析方面。此外,还对英国文学进行了评述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Temporal Bone Meningioma Presenting as Chronic Mastoiditis and Sigmoid Sinus Thrombosis: Report of a Case with Literature Analysis
Primary extra cranial meningioma of the ear and temporal bone are exceedingly rare, making up less than 1% of all meningiomas. Histologically, they are indistinguishable from their intracranial counterpart. The histopathologic diagnosis is often challenging, and the differential diagnosis for neoplasms in this unusual location is quite extensive. We report a 64-year-old male patient with history of seizures who presented with coalescing mastoiditis and sigmoid sinus thrombosis. CT and MRI findings were suggestive of a chronic inflammatory process. Operative findings included a flesh-colored mass extending from the mastoid antrum posteriorly towards the Sigmoid sinus. Intraoperative consultation was requested, yielding a diagnosis favoring squamous cell carcinoma, and the decision was made to end the procedure. Additional tissue was submitted for permanent evaluation, and biopsy demonstrated a grade 1 meningioma, supported by morphologic features and immunophenotype. The clinical and histologic findings of the patient are discussed, and we emphasize the challenging nature of this rare entity, particularly with regards to intraoperative analysis. In addition, English literature is reviewed.
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