微小肺脑膜样结节的临床病理和基因组特征。

IF 5.1 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Haochen Li , Zhicheng Huang , Yadong Wang , Chao Guo , Xiaoyu Li , Weixun Zhou , Sha Wang , Na Bai , Hanlin Chen , Bowen Li , Daoyun Wang , Zhibo Zheng , Zhongxing Bing , Yang Song , Yuan Xu , Guanghua Huang , Ka Luk Fung , Lan Song , Naixin Liang , Shanqing Li
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引用次数: 0

摘要

肺小脑膜样结节(MPMNs)是一种良性肺病变,其组织学特征与脑膜上皮相似。MPMNs的影像学特征与恶性结节相似,常被误诊。MPMNs的发病机制尚不清楚,目前的研究主要集中在有限数量的基因突变上,缺乏对其突变景观的全面分析。我们收集了近5年来在北京协和医院病理检查的88例患者中134例MPMNs。我们对6例患者的12个mpmn和7个腺癌病变进行了全外显子组测序(WES)。在我们的pump - mpmn队列中,我们提供了mpmn患者的临床、病理、放射学和随访特征。我们的研究证实了三种经典的MPMN诊断标记(EMA、PR和Vimentin)和新的标记物SSTR2的病理诊断价值。提示术前PET-CT的鉴别诊断价值。我们还根据不同的发现方法将MPMNs分为四种类型,并验证了传统和新型免疫组织化学标志物的诊断价值。全外显子组测序(WES)显示,MPMNs中含有丰富的细胞周期和细胞骨架组装途径的突变,而经典的脑膜瘤相关突变,如NF2,未被检测到。这些发现为MPMNs起源于反应性增殖而不是与脑膜瘤有共同起源的假设提供了新的证据,有助于临床医生和病理学家更好地了解MPMNs,减少误诊,改善患者护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinicopathologic and Genomic Characteristics of Minute Pulmonary Meningothelial-like Nodules
Minute pulmonary meningothelial-like nodules (MPMNs) are benign lung lesions with histologic characteristics similar to meningeal epithelium. MPMNs often lead to misdiagnosis for their similar radiologic characteristics to malignant nodules. The pathogenesis of MPMNs remains unclear, and this research primarily focused on mutations in a limited number of genes, lacking a comprehensive analysis of their mutational landscape. We collected 134 MPMNs from 88 patients with pathologic examinations at Peking Union Medical College Hospital in the past 5 years. We performed whole-exome sequencing on 12 MPMNs and 7 adenocarcinoma lesions from 6 patients. In our PUMCH-MPMN cohort, we provided clinical, pathologic, radiologic, and follow-up characteristics of patients with MPMNs. Our study demonstrated the pathologic diagnostic value of 3 classic MPMN diagnostic markers (epithelial membrane antigen, progesterone receptor, and vimentin) and the novel marker somatostatin receptor 2. It also suggested the preoperative differential diagnostic value of positron emission tomography/computed tomography. We also classified MPMNs into 4 types based on different discovery methods and verified the diagnostic value of traditional and novel immunohistochemical markers. We performed whole-exome sequencing and revealed that MPMNs harbor mutations enriched in cell cycle and cytoskeleton assembly pathways. On the other hand, classical meningioma-related mutations, such as NF2 mutations, were not detected. These findings provide new evidence for the hypothesis that MPMNs arise from reactive proliferation rather than share a common origin with meningiomas, contributing to a better understanding of MPMNs among clinicians and pathologists, reducing misdiagnosis, and improving patient care.
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来源期刊
Laboratory Investigation
Laboratory Investigation 医学-病理学
CiteScore
8.30
自引率
0.00%
发文量
125
审稿时长
2 months
期刊介绍: Laboratory Investigation is an international journal owned by the United States and Canadian Academy of Pathology. Laboratory Investigation offers prompt publication of high-quality original research in all biomedical disciplines relating to the understanding of human disease and the application of new methods to the diagnosis of disease. Both human and experimental studies are welcome.
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