{"title":"炎性横纹肌母细胞瘤:综述与最新进展","authors":"Andrew L. Folpe","doi":"10.1016/j.semdp.2025.150917","DOIUrl":null,"url":null,"abstract":"<div><div>Inflammatory rhabdomyoblastic tumors (IRMT), clinicopathologically and genetically distinct skeletal muscle tumors of borderline malignancy. These rare tumors were originally believed to represent “inflammatory leiomyosarcomas” and have also been reported as “histiocyte-rich rhabdomyoblastic tumor” and “low-grade inflammatory myogenic tumor”. In addition to representing the only skeletal muscle tumor of borderline malignancy, IRMT may also rarely progress to fully malignant rhabdomyosarcoma. The clinicopathologic, immunohistochemical and molecular genetic features of IRMT and rhabdomyosarcomas arising from IRMT are reviewed.</div></div>","PeriodicalId":49548,"journal":{"name":"Seminars in Diagnostic Pathology","volume":"42 4","pages":"Article 150917"},"PeriodicalIF":2.9000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Inflammatory rhabdomyoblastic tumor: A review and update\",\"authors\":\"Andrew L. Folpe\",\"doi\":\"10.1016/j.semdp.2025.150917\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Inflammatory rhabdomyoblastic tumors (IRMT), clinicopathologically and genetically distinct skeletal muscle tumors of borderline malignancy. These rare tumors were originally believed to represent “inflammatory leiomyosarcomas” and have also been reported as “histiocyte-rich rhabdomyoblastic tumor” and “low-grade inflammatory myogenic tumor”. In addition to representing the only skeletal muscle tumor of borderline malignancy, IRMT may also rarely progress to fully malignant rhabdomyosarcoma. The clinicopathologic, immunohistochemical and molecular genetic features of IRMT and rhabdomyosarcomas arising from IRMT are reviewed.</div></div>\",\"PeriodicalId\":49548,\"journal\":{\"name\":\"Seminars in Diagnostic Pathology\",\"volume\":\"42 4\",\"pages\":\"Article 150917\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Seminars in Diagnostic Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S074025702500053X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seminars in Diagnostic Pathology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S074025702500053X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
Inflammatory rhabdomyoblastic tumor: A review and update
Inflammatory rhabdomyoblastic tumors (IRMT), clinicopathologically and genetically distinct skeletal muscle tumors of borderline malignancy. These rare tumors were originally believed to represent “inflammatory leiomyosarcomas” and have also been reported as “histiocyte-rich rhabdomyoblastic tumor” and “low-grade inflammatory myogenic tumor”. In addition to representing the only skeletal muscle tumor of borderline malignancy, IRMT may also rarely progress to fully malignant rhabdomyosarcoma. The clinicopathologic, immunohistochemical and molecular genetic features of IRMT and rhabdomyosarcomas arising from IRMT are reviewed.
期刊介绍:
Each issue of Seminars in Diagnostic Pathology offers current, authoritative reviews of topics in diagnostic anatomic pathology. The Seminars is of interest to pathologists, clinical investigators and physicians in practice.