{"title":"MRI上原发性滑膜肉瘤的病例系列及文献回顾。","authors":"Maya Sedaghat, Sam Sedaghat","doi":"10.5114/pjr.2023.130048","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Simple MRI features are mandatory to facilitate the diagnostics of synovial sarcomas, especially for radiolo-gists outside multidisciplinary sarcoma centres. In this case-series and review, we investigate the main appearance of synovial sarcoma on MRI.</p><p><strong>Material and methods: </strong>Fifteen histologically proven primary synovial sarcomas who underwent MRI at 2 different sarcoma centres were included in this case series. Patients and their primary synovial sarcomas were examined for age, localization, mean tumour size (in mm), histological grade (G - according to the Fédération Nationale des Centres de Lutte Contre Le Cancer [FNCLCC]), configuration, T2 signal intensity, presence/absence of \"triple sign\", heterogeneity/homogeneity, borders (well-defined or infiltrative), and intensity of contrast enhancement on MRI. Additionally, a comprehensive literature review to identify observational studies, reviews, and case-reports assessing MRI features of primary synovial sarcoma was performed.</p><p><strong>Results: </strong>The mean age of the patients was 47.6 years (SD: 17.2). The mean size of primary synovial sarcoma was 59.3 mm (SD: 42). Primary synovial sarcomas were significantly most often multilobulated (<i>n</i> = 12, <i>p</i> < 0.01), heterogeneous (<i>n</i> = 10), and infiltrative (<i>n</i> = 9). Additionally, 3 other primary synovial sarcomas showed the following configurations: ovoid/nodular (<i>n</i> = 2) and fascicular (<i>n</i> = 1). Ovoid/nodular synovial sarcomas were solely depicted as homogeneous with well-defined borders. All tumours showed T2 hyperintense signal and presented with marked contrast enhancement.</p><p><strong>Conclusions: </strong>Primary synovial sarcomas are mainly multilobulated, heterogeneous, and infiltrative tumours. In minor cases, ovoid/nodular or fascicular configurations occur. Knowing the main appearance of synovial sarcoma can help facilitate the diagnostics of primary synovial sarcomas.</p>","PeriodicalId":47128,"journal":{"name":"Polish Journal of Radiology","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f1/62/PJR-88-51147.PMC10415809.pdf","citationCount":"1","resultStr":"{\"title\":\"Primary synovial sarcoma on MRI - a case series and review of the literature.\",\"authors\":\"Maya Sedaghat, Sam Sedaghat\",\"doi\":\"10.5114/pjr.2023.130048\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Simple MRI features are mandatory to facilitate the diagnostics of synovial sarcomas, especially for radiolo-gists outside multidisciplinary sarcoma centres. In this case-series and review, we investigate the main appearance of synovial sarcoma on MRI.</p><p><strong>Material and methods: </strong>Fifteen histologically proven primary synovial sarcomas who underwent MRI at 2 different sarcoma centres were included in this case series. Patients and their primary synovial sarcomas were examined for age, localization, mean tumour size (in mm), histological grade (G - according to the Fédération Nationale des Centres de Lutte Contre Le Cancer [FNCLCC]), configuration, T2 signal intensity, presence/absence of \\\"triple sign\\\", heterogeneity/homogeneity, borders (well-defined or infiltrative), and intensity of contrast enhancement on MRI. Additionally, a comprehensive literature review to identify observational studies, reviews, and case-reports assessing MRI features of primary synovial sarcoma was performed.</p><p><strong>Results: </strong>The mean age of the patients was 47.6 years (SD: 17.2). The mean size of primary synovial sarcoma was 59.3 mm (SD: 42). Primary synovial sarcomas were significantly most often multilobulated (<i>n</i> = 12, <i>p</i> < 0.01), heterogeneous (<i>n</i> = 10), and infiltrative (<i>n</i> = 9). Additionally, 3 other primary synovial sarcomas showed the following configurations: ovoid/nodular (<i>n</i> = 2) and fascicular (<i>n</i> = 1). Ovoid/nodular synovial sarcomas were solely depicted as homogeneous with well-defined borders. All tumours showed T2 hyperintense signal and presented with marked contrast enhancement.</p><p><strong>Conclusions: </strong>Primary synovial sarcomas are mainly multilobulated, heterogeneous, and infiltrative tumours. In minor cases, ovoid/nodular or fascicular configurations occur. Knowing the main appearance of synovial sarcoma can help facilitate the diagnostics of primary synovial sarcomas.</p>\",\"PeriodicalId\":47128,\"journal\":{\"name\":\"Polish Journal of Radiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f1/62/PJR-88-51147.PMC10415809.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polish Journal of Radiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5114/pjr.2023.130048\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polish Journal of Radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5114/pjr.2023.130048","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 1
摘要
目的:简单的MRI特征是必要的,以促进滑膜肉瘤的诊断,特别是对于多学科肉瘤中心以外的放射科医生。在这个病例系列和回顾中,我们探讨滑膜肉瘤在MRI上的主要表现。材料和方法:15例组织学证实的原发性滑膜肉瘤患者在2个不同的肉瘤中心接受了MRI检查。检查患者及其原发滑膜肉瘤的年龄、定位、平均肿瘤大小(毫米)、组织学分级(根据FNCLCC标准G -)、形态、T2信号强度、是否存在“三重征象”、异质性/均匀性、边界(明确或浸润)以及MRI对比增强强度。此外,我们还进行了全面的文献综述,以确定观察性研究、综述和评估原发性滑膜肉瘤MRI特征的病例报告。结果:患者平均年龄47.6岁(SD: 17.2)。原发滑膜肉瘤的平均大小为59.3 mm (SD: 42)。原发性滑膜肉瘤最常见的是多分叶状(n = 12, p < 0.01)、异质性(n = 10)和浸润性(n = 9)。此外,其他3例原发性滑膜肉瘤表现出以下形态:卵状/结节状(n = 2)和束状(n = 1)。卵状/结节状滑膜肉瘤仅表现为均匀性,边界明确。所有肿瘤均呈T2高信号,并有明显的对比增强。结论:原发性滑膜肉瘤以多分叶性、异质性和浸润性肿瘤为主。在少数情况下,出现卵球形/结节状或束状构型。了解滑膜肉瘤的主要表现有助于原发性滑膜肉瘤的诊断。
Primary synovial sarcoma on MRI - a case series and review of the literature.
Purpose: Simple MRI features are mandatory to facilitate the diagnostics of synovial sarcomas, especially for radiolo-gists outside multidisciplinary sarcoma centres. In this case-series and review, we investigate the main appearance of synovial sarcoma on MRI.
Material and methods: Fifteen histologically proven primary synovial sarcomas who underwent MRI at 2 different sarcoma centres were included in this case series. Patients and their primary synovial sarcomas were examined for age, localization, mean tumour size (in mm), histological grade (G - according to the Fédération Nationale des Centres de Lutte Contre Le Cancer [FNCLCC]), configuration, T2 signal intensity, presence/absence of "triple sign", heterogeneity/homogeneity, borders (well-defined or infiltrative), and intensity of contrast enhancement on MRI. Additionally, a comprehensive literature review to identify observational studies, reviews, and case-reports assessing MRI features of primary synovial sarcoma was performed.
Results: The mean age of the patients was 47.6 years (SD: 17.2). The mean size of primary synovial sarcoma was 59.3 mm (SD: 42). Primary synovial sarcomas were significantly most often multilobulated (n = 12, p < 0.01), heterogeneous (n = 10), and infiltrative (n = 9). Additionally, 3 other primary synovial sarcomas showed the following configurations: ovoid/nodular (n = 2) and fascicular (n = 1). Ovoid/nodular synovial sarcomas were solely depicted as homogeneous with well-defined borders. All tumours showed T2 hyperintense signal and presented with marked contrast enhancement.
Conclusions: Primary synovial sarcomas are mainly multilobulated, heterogeneous, and infiltrative tumours. In minor cases, ovoid/nodular or fascicular configurations occur. Knowing the main appearance of synovial sarcoma can help facilitate the diagnostics of primary synovial sarcomas.