Primary uterine Ewing sarcoma – A case report
Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdomin...
Ausführliche Beschreibung
Autor*in: |
Yen-Chen Wu [verfasserIn] Yu-Chien Kao [verfasserIn] Ching-Wen Chang [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Übergeordnetes Werk: |
In: Taiwanese Journal of Obstetrics & Gynecology - Elsevier, 2017, 60(2021), 1, Seite 142-144 |
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Übergeordnetes Werk: |
volume:60 ; year:2021 ; number:1 ; pages:142-144 |
Links: |
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DOI / URN: |
10.1016/j.tjog.2020.11.022 |
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10.1016/j.tjog.2020.11.022 doi (DE-627)DOAJ07302404X (DE-599)DOAJa8e0012ab78d444cb19d9919d70ce755 DE-627 ger DE-627 rakwb eng RG1-991 Yen-Chen Wu verfasserin aut Primary uterine Ewing sarcoma – A case report 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdominal hysterectomy, and bilateral salpingo-oophorectomy and following adjuvant chemotherapy with 6 cycles of vincristine, doxorubicin, and cyclophosphamide, achieving complete remission for one year. Conclusion: Complete resection for EFT is the first choice of treatment, regardless of their origins. Adjuvant chemotherapy or radiotherapy is mandatory if needed. Due to rarity of the disease, this report re-emphasizes the accurate diagnosis and appropriate treatment for these unusual tumor types occurred in female genital organs. Ewing family of tumors Peripheral primitive neuroectodermal tumors Primary Ewing sarcoma Uterus Gynecology and obstetrics Yu-Chien Kao verfasserin aut Ching-Wen Chang verfasserin aut In Taiwanese Journal of Obstetrics & Gynecology Elsevier, 2017 60(2021), 1, Seite 142-144 (DE-627)500021422 (DE-600)2202946-1 10284559 nnns volume:60 year:2021 number:1 pages:142-144 https://doi.org/10.1016/j.tjog.2020.11.022 kostenfrei https://doaj.org/article/a8e0012ab78d444cb19d9919d70ce755 kostenfrei http://www.sciencedirect.com/science/article/pii/S1028455920302989 kostenfrei https://doaj.org/toc/1028-4559 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_2014 GBV_ILN_2068 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 60 2021 1 142-144 |
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10.1016/j.tjog.2020.11.022 doi (DE-627)DOAJ07302404X (DE-599)DOAJa8e0012ab78d444cb19d9919d70ce755 DE-627 ger DE-627 rakwb eng RG1-991 Yen-Chen Wu verfasserin aut Primary uterine Ewing sarcoma – A case report 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdominal hysterectomy, and bilateral salpingo-oophorectomy and following adjuvant chemotherapy with 6 cycles of vincristine, doxorubicin, and cyclophosphamide, achieving complete remission for one year. Conclusion: Complete resection for EFT is the first choice of treatment, regardless of their origins. Adjuvant chemotherapy or radiotherapy is mandatory if needed. Due to rarity of the disease, this report re-emphasizes the accurate diagnosis and appropriate treatment for these unusual tumor types occurred in female genital organs. Ewing family of tumors Peripheral primitive neuroectodermal tumors Primary Ewing sarcoma Uterus Gynecology and obstetrics Yu-Chien Kao verfasserin aut Ching-Wen Chang verfasserin aut In Taiwanese Journal of Obstetrics & Gynecology Elsevier, 2017 60(2021), 1, Seite 142-144 (DE-627)500021422 (DE-600)2202946-1 10284559 nnns volume:60 year:2021 number:1 pages:142-144 https://doi.org/10.1016/j.tjog.2020.11.022 kostenfrei https://doaj.org/article/a8e0012ab78d444cb19d9919d70ce755 kostenfrei http://www.sciencedirect.com/science/article/pii/S1028455920302989 kostenfrei https://doaj.org/toc/1028-4559 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_2014 GBV_ILN_2068 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 60 2021 1 142-144 |
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10.1016/j.tjog.2020.11.022 doi (DE-627)DOAJ07302404X (DE-599)DOAJa8e0012ab78d444cb19d9919d70ce755 DE-627 ger DE-627 rakwb eng RG1-991 Yen-Chen Wu verfasserin aut Primary uterine Ewing sarcoma – A case report 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdominal hysterectomy, and bilateral salpingo-oophorectomy and following adjuvant chemotherapy with 6 cycles of vincristine, doxorubicin, and cyclophosphamide, achieving complete remission for one year. Conclusion: Complete resection for EFT is the first choice of treatment, regardless of their origins. Adjuvant chemotherapy or radiotherapy is mandatory if needed. Due to rarity of the disease, this report re-emphasizes the accurate diagnosis and appropriate treatment for these unusual tumor types occurred in female genital organs. Ewing family of tumors Peripheral primitive neuroectodermal tumors Primary Ewing sarcoma Uterus Gynecology and obstetrics Yu-Chien Kao verfasserin aut Ching-Wen Chang verfasserin aut In Taiwanese Journal of Obstetrics & Gynecology Elsevier, 2017 60(2021), 1, Seite 142-144 (DE-627)500021422 (DE-600)2202946-1 10284559 nnns volume:60 year:2021 number:1 pages:142-144 https://doi.org/10.1016/j.tjog.2020.11.022 kostenfrei https://doaj.org/article/a8e0012ab78d444cb19d9919d70ce755 kostenfrei http://www.sciencedirect.com/science/article/pii/S1028455920302989 kostenfrei https://doaj.org/toc/1028-4559 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_2014 GBV_ILN_2068 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 60 2021 1 142-144 |
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10.1016/j.tjog.2020.11.022 doi (DE-627)DOAJ07302404X (DE-599)DOAJa8e0012ab78d444cb19d9919d70ce755 DE-627 ger DE-627 rakwb eng RG1-991 Yen-Chen Wu verfasserin aut Primary uterine Ewing sarcoma – A case report 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdominal hysterectomy, and bilateral salpingo-oophorectomy and following adjuvant chemotherapy with 6 cycles of vincristine, doxorubicin, and cyclophosphamide, achieving complete remission for one year. Conclusion: Complete resection for EFT is the first choice of treatment, regardless of their origins. Adjuvant chemotherapy or radiotherapy is mandatory if needed. Due to rarity of the disease, this report re-emphasizes the accurate diagnosis and appropriate treatment for these unusual tumor types occurred in female genital organs. Ewing family of tumors Peripheral primitive neuroectodermal tumors Primary Ewing sarcoma Uterus Gynecology and obstetrics Yu-Chien Kao verfasserin aut Ching-Wen Chang verfasserin aut In Taiwanese Journal of Obstetrics & Gynecology Elsevier, 2017 60(2021), 1, Seite 142-144 (DE-627)500021422 (DE-600)2202946-1 10284559 nnns volume:60 year:2021 number:1 pages:142-144 https://doi.org/10.1016/j.tjog.2020.11.022 kostenfrei https://doaj.org/article/a8e0012ab78d444cb19d9919d70ce755 kostenfrei http://www.sciencedirect.com/science/article/pii/S1028455920302989 kostenfrei https://doaj.org/toc/1028-4559 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_2014 GBV_ILN_2068 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 60 2021 1 142-144 |
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Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdominal hysterectomy, and bilateral salpingo-oophorectomy and following adjuvant chemotherapy with 6 cycles of vincristine, doxorubicin, and cyclophosphamide, achieving complete remission for one year. Conclusion: Complete resection for EFT is the first choice of treatment, regardless of their origins. Adjuvant chemotherapy or radiotherapy is mandatory if needed. Due to rarity of the disease, this report re-emphasizes the accurate diagnosis and appropriate treatment for these unusual tumor types occurred in female genital organs. |
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Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdominal hysterectomy, and bilateral salpingo-oophorectomy and following adjuvant chemotherapy with 6 cycles of vincristine, doxorubicin, and cyclophosphamide, achieving complete remission for one year. Conclusion: Complete resection for EFT is the first choice of treatment, regardless of their origins. Adjuvant chemotherapy or radiotherapy is mandatory if needed. Due to rarity of the disease, this report re-emphasizes the accurate diagnosis and appropriate treatment for these unusual tumor types occurred in female genital organs. |
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Objective: Ewing sarcoma is a type of neuroectodermal tumors (Ewing family of tumors-EFT) that mostly affect the bone or soft tissue. Primary uterine Ewing sarcoma is extremely rare. Case report: We report a case of a primary uterine Ewing sarcoma in a 46-year-old patient, treated with total abdominal hysterectomy, and bilateral salpingo-oophorectomy and following adjuvant chemotherapy with 6 cycles of vincristine, doxorubicin, and cyclophosphamide, achieving complete remission for one year. Conclusion: Complete resection for EFT is the first choice of treatment, regardless of their origins. Adjuvant chemotherapy or radiotherapy is mandatory if needed. Due to rarity of the disease, this report re-emphasizes the accurate diagnosis and appropriate treatment for these unusual tumor types occurred in female genital organs. |
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|
score |
7.401454 |