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肺黏液表皮样癌:一例病例报告及文献综述

Mucoepidermoid carcinoma of the lung: a case report and literature review.

作者信息

Alsidawi S, Morris J C, Wikenheiser-Brokamp K A, Starnes S L, Karim N A

机构信息

Department of Internal Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.

出版信息

Case Rep Oncol Med. 2013;2013:625243. doi: 10.1155/2013/625243. Epub 2013 Nov 4.

Abstract

Introduction. Mucoepidermoid carcinoma (MEC) of the lung is a rare form of lung cancer that is classified into low grade and high grade based on histological features. Surgical resection is the primary treatment for low-grade MEC with excellent outcomes, while high-grade MEC is a more aggressive form of malignancy. Clinical Case. We report a case of a 46-year-old woman who presented with dyspnea on exertion. Imaging studies revealed a mass involving the right upper lobe bronchus. Bronchoscopy, surgical resection, and pathological examination revealed a low-grade MEC with tumor-free margins. No adjuvant treatment was given. Discussion. Primary pulmonary MEC is a rare type of lung cancer with only few reported cases. This patient illustrates a typical presentation for low-grade MEC wherein surgical resection is considered curative. In contrast, high-grade MEC is a more aggressive malignancy with a poorer outcome. The role of targeted therapy directed against EGFR or a novel CRTC1-MAML2 fusion protein expressed in some high-grade tumors is yet to be determined.

摘要

引言。肺黏液表皮样癌(MEC)是肺癌的一种罕见形式,根据组织学特征分为低级别和高级别。手术切除是低级别MEC的主要治疗方法,预后良好,而高级别MEC是一种侵袭性更强的恶性肿瘤。临床病例。我们报告一例46岁女性,表现为劳力性呼吸困难。影像学检查显示右肺上叶支气管有肿块。支气管镜检查、手术切除及病理检查显示为低级别MEC,切缘无肿瘤。未给予辅助治疗。讨论。原发性肺MEC是一种罕见的肺癌类型,报道病例很少。该患者展示了低级别MEC的典型表现,手术切除被认为可治愈。相比之下,高级别MEC是一种侵袭性更强的恶性肿瘤,预后较差。针对表皮生长因子受体(EGFR)或某些高级别肿瘤中表达的新型CRTC1-MAML2融合蛋白的靶向治疗作用尚未确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aac/3834989/83a5f98b0e72/CRIM.ONCMED2013-625243.001.jpg

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