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
{"title":"微小肺脑膜样结节的临床病理和基因组特征。","authors":"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","doi":"10.1016/j.labinv.2025.104188","DOIUrl":null,"url":null,"abstract":"<div><div>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 <em>NF2</em> 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.</div></div>","PeriodicalId":17930,"journal":{"name":"Laboratory Investigation","volume":"105 9","pages":"Article 104188"},"PeriodicalIF":5.1000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinicopathologic and Genomic Characteristics of Minute Pulmonary Meningothelial-like Nodules\",\"authors\":\"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\",\"doi\":\"10.1016/j.labinv.2025.104188\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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 <em>NF2</em> 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.</div></div>\",\"PeriodicalId\":17930,\"journal\":{\"name\":\"Laboratory Investigation\",\"volume\":\"105 9\",\"pages\":\"Article 104188\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2025-04-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laboratory Investigation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0023683725000984\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laboratory Investigation","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0023683725000984","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
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.
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.