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一例耵聍腺瘤中Glut-1、HIF-1α、PI3K和p-Akt的表达

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

作者信息

Shen Wan-Qin, Cheng Ke-Jia, Bao Yang-Yang, Zhou Shui-Hong, Yao Hong-Tian

机构信息

Department of Otolaryngology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, 310003, China.

出版信息

Head Neck Oncol. 2012 May 2;4:18. doi: 10.1186/1758-3284-4-18.

Abstract

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.

摘要

目的

外耳道耵聍腺瘤是一种经组织学诊断的罕见肿瘤类型。然而,这些肿瘤的临床行为仍存在争议。在此,我们报告一例外耳道耵聍腺瘤病例及一种缺氧标志物的表达情况。

病例报告

一名78岁男性,有右耳反复流脓6个月的病史。采用经耳道入路手术,完整切除肿物。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呈阳性。术后27个月的最后一次随访时无复发迹象。

结论

外耳道耵聍腺瘤是一种罕见肿瘤。首选治疗方法是切缘清晰的广泛局部切除。据我们所知,这是外耳道耵聍腺瘤中Glut-1表达及PI3K/Akt通路的首例报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad83/3414790/8d60778da178/1758-3284-4-18-1.jpg

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