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A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management

机译:少见的内淋巴囊肿瘤病例:临床病理研究和外科治疗

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Objective. Endolymphatic sac tumor (ELST) is a rare neoplasm arising from the intrapetrous portion of the endolymphatic sac, either isolated or in association with the von Hippel-Lindau disease. We report a sporadic case of ELST with an overview of the literature and a discussion of clinic-radiological, histopathologic, and surgical findings.Case Report. A young woman presented with a progressive hearing loss in the left ear. Otoscopy showed a reddish, bleeding hypotympanic mass. CT demonstrated an expansile lytic mastoid lesion extending to the middle ear, with bone erosion. MRI confirmed a lesion of increased signal on T1-weighted sequences. The patient underwent a canal wall-down tympanoplasty with complete removal of the tumor. Histopathology was consistent with a papillary ELST. Immunohistochemistry was positive for cytokeratin and chromogranin A.Conclusion. This paper highlights the rarity of ELST, the need for an accurate neuroradiological and immunohistochemical study at the early stages, and the timeliness of surgical treatment.
机译:目的。内淋巴囊肿瘤(ELST)是一种罕见的肿瘤,由内淋巴囊的石内部分衍生而来,既可以分离也可以与von Hippel-Lindau病相关。我们报道了散发性ELST病例,其中包括文献综述以及对临床放射学,组织病理学和手术结果的讨论。一名年轻女子的左耳听力逐渐下降。耳镜检查发现鼓室出血呈红色,出血。 CT表现为扩张性溶解性乳突状病变,延伸至中耳,伴有骨侵蚀。 MRI证实了T1加权序列上信号增加的病变。患者进行了根管下腔鼓膜成形术,并完全切除了肿瘤。组织病理学与乳头状ELST一致。细胞角蛋白和嗜铬粒蛋白A的免疫组织化学阳性。本文强调了ELST的稀缺性,在早期阶段需要进行准确的神经放射学和免疫组织化学研究的必要性以及手术治疗的及时性。

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