Suppr超能文献

继发于伴有BCOR基因突变的典型肺类癌的库欣综合征:一例报告

Cushing's syndrome secondary to typical pulmonary carcinoid with mutation in BCOR gene: A case report.

作者信息

Wu Yimin, Yue Lan, Li Jinfan, Yuan Mingjing, Chai Ying

机构信息

Department of Thoracic Surgery, the Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 3D Medicines Corporation, Shanghai, China.

出版信息

Medicine (Baltimore). 2017 Aug;96(34):e7870. doi: 10.1097/MD.0000000000007870.

Abstract

RATIONALE

Typical pulmonary carcinoid is a kind of low-grade malignancy neuroendocrine tumor. Cushing's syndrome is a very rare clinical feature of typical pulmonary carcinoid caused by hypercorticism. Complete tumor resection is the standard curative treatment for primary typical pulmonary carcinoid. However, our knowledge on the gene level of typical pulmonary carcinoid is limited.

PATIENT CONCERNS

A 42-year-old man was admitted to our hospital for progressive weight gain within one year. No other obvious symptoms were obsessed in this patient. He was clinical diagnosed with ectopic adrenocorticotropic hormone syndrome through hormonal tests and imaging exams. Positron emission tomography-computed tomography detected a pulmonary nodule localized in the middle lobe of the lung and it is thought to be the ectopic source.

INTERVENTION

This patient received a pulmonary wedge resection. After the surgery, a genetic sequencing was performed and it reported a mutation (S1240Cfs*21) in the BCOR gene.

DIAGNOSIS

Postoperative pathology confirmed the diagnosis of ACTH-producing typical pulmonary carcinoid.

OUTCOMES

The patient had a smooth postoperative course and no recurrence of the tumor was found for 3 years.

LESSONS

Mutation in BCOR gene is quite common in pulmonary neuroendocrine tumor and it has been proven to play a role in the development of some tumor. We herein first report BCOR gene mutation in Cushing's syndrome secondary to TPC and it may become a promising therapeutic target in the future.

摘要

理论依据

典型肺类癌是一种低级别恶性神经内分泌肿瘤。库欣综合征是典型肺类癌由皮质醇增多症引起的一种非常罕见的临床特征。完整肿瘤切除是原发性典型肺类癌的标准治愈性治疗方法。然而,我们对典型肺类癌基因水平的了解有限。

患者情况

一名42岁男性因一年内体重进行性增加入院。该患者未发现其他明显症状。通过激素检测和影像学检查临床诊断为异位促肾上腺皮质激素综合征。正电子发射断层扫描-计算机断层扫描检测到一个位于肺中叶的肺结节,认为是异位来源。

干预措施

该患者接受了肺楔形切除术。术后进行了基因测序,报告显示BCOR基因存在突变(S1240Cfs*21)。

诊断结果

术后病理证实为分泌促肾上腺皮质激素的典型肺类癌。

治疗结果

患者术后恢复顺利,3年内未发现肿瘤复发。

经验教训

BCOR基因突变在肺神经内分泌肿瘤中相当常见,并且已被证明在某些肿瘤的发生发展中起作用。我们在此首次报告了继发于典型肺类癌的库欣综合征中的BCOR基因突变,它可能在未来成为一个有前景的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8453/5572024/eb8b4f5f083a/medi-96-e7870-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验