谷氨酸-1、HIF-1α、PI3K和p-Akt在耵聍腺瘤中的表达。

Wan-Qin Shen, Ke-Jia Cheng, Yang-Yang Bao, Shui-Hong Zhou, Hong-Tian Yao
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引用次数: 16

摘要

目的:外耳道耵聍腺瘤是一种罕见的经组织学诊断的肿瘤。然而,这些肿瘤的临床表现仍然存在争议。在此,我们报告一例EAC的耵聍腺瘤和缺氧标志物的表达。病例报告:78岁男性,右耳复发性耳漏6个月。手术通过经气管入路完全切除肿块。组织病理学显示为耵聍腺瘤。肿瘤细胞CK、S-100蛋白、Glut-1、HIF-1α、PI3K和p-Akt均呈阳性。术后27个月随访无复发迹象。结论:EAC的耵聍腺瘤是一种罕见的肿瘤。治疗的选择是广泛的局部切除与明确的边界。据我们所知,这是关于Glut-1表达和PI3K/Akt通路在EAC耵聍腺瘤中的首次报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Expression of Glut-1, HIF-1α, PI3K and p-Akt in a case of ceruminous adenoma.

Expression of Glut-1, HIF-1α, PI3K and p-Akt in a case of ceruminous adenoma.

Expression of Glut-1, HIF-1α, PI3K and p-Akt in a case of ceruminous adenoma.

Objectives: Ceruminous adenoma of the external auditory canal (EAC) is a rare type of tumour that is diagnosed histologically. However, the clinical behaviour of these tumours remains controversial. Here, we report a case of ceruminous adenoma of the EAC and expression of a hypoxia marker.

Case report: A 78-year-old man presented with a 6-month history of recurrent otorrhoea in the right ear. Surgery was performed by the transmeatal approach with total removal of the mass. Histopathology revealed a ceruminous adenoma. Tumour cells were positive for CK, S-100 protein, Glut-1, HIF-1α, PI3K and p-Akt. There was no evidence of recurrence at last follow-up 27 months after the operation.

Conclusions: Ceruminous adenoma of the EAC is a rare tumour. The treatment of choice is wide local excision with clear margins. To our knowledge, this is the first report of Glut-1 expression and the PI3K/Akt pathway in ceruminous adenoma of the EAC.

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