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      An exploratory study of CT-guided percutaneous radiofrequency ablation for stage I thymoma

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          Abstract

          Background

          Thymoma is a rare tumor that originates from thymic epithelial cells and is usually associated with myasthenia gravis. Radiofrequency ablation (RFA) is a minimally invasive and curative treatment for other tumors, but RFA has not been used for the early treatment of thymoma.

          Methods

          The current study included 13 patients with stage I thymoma who were not candidates for surgical resection or video-assisted thoracoscopic surgery (VATS). All patients underwent first-line CT-guided percutaneous RFA. The feasibility and therapeutic effects of the intervention were thoroughly documented.

          Results

          All tumors were completely ablated (13 / 13, 100%). During follow-up (median 80.5 months, range, 64.6–116.9 months), only 1 of the 13 patients had recurrence of thymoma (1 / 13, 7.7%) at 35.5 months after the initial ablation. There were no surgery-related deaths after RFA treatment. The most common complications were fever (13 / 13, 100%) and pain (13 / 13, 100%). There was only one patient who occurred severe puncture-related bleeding during the procedure that needed blood transfusion and intravascular embolization of the punctured-injured vessel.

          Conclusion

          CT-guided percutaneous RFA for treatment of stage I thymoma is associated with minor trauma, few complications and good treatment outcomes.

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          Most cited references18

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          Malignant thymoma in the United States: demographic patterns in incidence and associations with subsequent malignancies.

          The cause of thymoma is unknown. No population-based study has described demographic patterns of thymoma incidence. Previous reports have linked thymoma with diverse subsequent malignancies, but these associations are uncertain. We used Surveillance, Epidemiology and End Results (SEER) data to study the incidence of malignant thymoma by sex, age and race in the United States (1973-1998). Incidence was modeled with joinpoint regression (for age) and Poisson regression. We also used SEER data to compare malignancies following thymoma diagnosis with those expected from general population rates, calculating the standardized incidence ratio (SIR, observed/expected cases) to measure risk. The overall incidence of malignant thymoma was 0.15 per 100000 person-years (849 cases). Thymoma incidence increased into the 8th decade of age and then decreased. Incidence was higher in males than females (p=0.007) and was highest among Asians/Pacific Islanders (0.49 per 100000 person-years). Following thymoma, there were 66 malignancies (SIR 1.5, 95%CI 1.2-1.9). The most notable excess risk for subsequent malignancy was for non-Hodgkin's lymphoma (B immunophenotype) where the SIR was 4.7 (95%CI 1.9-9.6, 7 cases). There were also excess digestive system cancers (SIR 1.8, 95%CI 1.1-2.9) and soft tissue sarcomas (SIR 11.1, 1.3-40.1). No other cancers were increased after thymoma. In conclusion, malignant thymoma is extremely rare. The peak in late adulthood deserves further study. Variation in incidence by race suggests a role for genetic factors. Our study did not demonstrate broadly increased risk for malignancies following thymoma. Copyright 2003 Wiley-Liss, Inc.
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            Follow-up study of thymomas with special reference to their clinical stages

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              Thymoma and thymic carcinomas.

              Thymomas (Ts) and thymic carcinomas (TCs) are rare tumours of the mediastinum with an incidence rate of 1.7/million per year in Europe. Histological classification is based on rate of non-malignant-appearing thymic epithelial cells and proportions of lymphocytes (A, AB, B1, B2, B3, and C), while staging system concerns localisation of the involved areas. Surgery is the mainstay of treatment with a 10-year survival of 80%, 78%, 75%, and 42% for stages I, II, III and IV, respectively, with an R0 resection. Radiotherapy has a role in selected cases (stage III patients or R1-2 residual) and platinum-based chemotherapy remains the standard of care for patients with advanced disease. A multimodality approach would be advisable when surgery is not recommended. Since molecular aberrations are poorly understood and few responses are reported, targeted therapies are yet being studied. In this review, we describe key aspects of clinical management for Ts and TCs.
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                Author and article information

                Contributors
                dongjun1@sysucc.org.cn
                qingzhoude1@hotmail.com
                changby3@mail.sysu.edu.cn
                huangjinsh@sysucc.org.cn
                654266759@qq.com
                caixiy@sysucc.org.cn
                hupl@sysucc.org.cn
                zhangb@sysucc.org.cn
                xialp@sysucc.org.cn
                862087343272 , wuph@sysucc.org.cn
                Journal
                Cancer Imaging
                Cancer Imaging
                Cancer Imaging
                BioMed Central (London )
                1740-5025
                1470-7330
                2 December 2019
                2 December 2019
                2019
                : 19
                : 80
                Affiliations
                [1 ]ISNI 0000 0004 1803 6191, GRID grid.488530.2, Department of Integrated Therapy in Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, , Sun Yat-sen University Cancer Center, ; Guangzhou, 510060 People’s Republic of China
                [2 ]GRID grid.452885.6, Department of Oncology, , The Third Affiliated Hospital of Wenzhou Medical University, ; Wansong Road, Ruian, 108 China
                [3 ]ISNI 0000 0004 1762 1794, GRID grid.412558.f, Department of Vascular Interventional Radiology, , the Third Affiliated Hospital of Sun Yat-sen University, ; Guangzhou, 510630 People’s Republic of China
                [4 ]GRID grid.452859.7, Department of Geriatric Medicine, , the Fifth Affiliated Hospital of Sun Yat-sen University, ; Guangzhou, 510630 People’s Republic of China
                [5 ]ISNI 0000 0004 1803 6191, GRID grid.488530.2, Department of Medical Imaging & Image Guided Therapy, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, , Sun Yat-sen University Cancer Center, ; Guangzhou, 510060 People’s Republic of China
                Article
                267
                10.1186/s40644-019-0267-8
                6889348
                31791411
                394283b3-db37-4fbc-9d07-03fc35124d06
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 7 January 2019
                : 22 November 2019
                Funding
                Funded by: National Natural Science Foundation of China Young Scientists Fund (CN)
                Award ID: 81601581
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 81600606
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                ct-guided,percutaneous radiofrequency ablation,early stage,thymoma

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