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Titlebook: Rare Sarcomas; Christine Chevreau,Antoine Italiano Book 2020 Springer Nature Switzerland AG 2020 chemotherapy.rare tumors.radiotherapy.sur

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發(fā)表于 2025-3-21 18:11:07 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Rare Sarcomas
編輯Christine Chevreau,Antoine Italiano
視頻videohttp://file.papertrans.cn/822/821272/821272.mp4
概述Examines rare sarcomas from oncologist‘s and pathologist‘s perspective.Discusses the management of rare sarcomas by medical teams.Written by experts in sarcoma specialist centres
圖書(shū)封面Titlebook: Rare Sarcomas;  Christine Chevreau,Antoine Italiano Book 2020 Springer Nature Switzerland AG 2020 chemotherapy.rare tumors.radiotherapy.sur
描述.This is a unique book focusing on the management of rare sarcomas, which pose an important challenge in Europe and in the US, as they represent nearly one quarter of all new diagnoses of cancer and have lower survival rates than common cancer. Discussing a range of tumors from clear cell and epithelioid sarcoma to solitary fibrous tumor and myxoid fibrosarcoma, this book provides invaluable expertise according to evidence-based guidelines and uses a patient-centered?multi-disciplinary approach..Each of the chapters discusses the forms of rare sarcomas both from an oncological and a pathological perspective. This book aims to help the sarcoma expert in improving the management, quality of care and outcome for patients with rare tumors, which have now been recognised as a public health priority..The authors are experts from specialist sarcoma centers focusing on the capacity to develop clinical guidelines, and to foster clinical, translational and epidemiologicalresearch for rare cancers..
出版日期Book 2020
關(guān)鍵詞chemotherapy; rare tumors; radiotherapy; surgery; fibrous tumor; clear cell sarcoma; solid tissue sarcoma
版次1
doihttps://doi.org/10.1007/978-3-030-24697-6
isbn_softcover978-3-030-24699-0
isbn_ebook978-3-030-24697-6
copyrightSpringer Nature Switzerland AG 2020
The information of publication is updating

書(shū)目名稱(chēng)Rare Sarcomas影響因子(影響力)




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沙發(fā)
發(fā)表于 2025-3-21 23:22:09 | 只看該作者
https://doi.org/10.1007/978-3-030-24697-6chemotherapy; rare tumors; radiotherapy; surgery; fibrous tumor; clear cell sarcoma; solid tissue sarcoma
板凳
發(fā)表于 2025-3-22 01:10:28 | 只看該作者
地板
發(fā)表于 2025-3-22 06:52:08 | 只看該作者
5#
發(fā)表于 2025-3-22 12:25:00 | 只看該作者
Christine Chevreau,Antoine ItalianoExamines rare sarcomas from oncologist‘s and pathologist‘s perspective.Discusses the management of rare sarcomas by medical teams.Written by experts in sarcoma specialist centres
6#
發(fā)表于 2025-3-22 16:14:14 | 只看該作者
Clear Cell Sarcoma,ndons and aponeuroses of distal extremities of relatively young individuals. This sarcoma is characterized by multiple local recurrences with late metastases, frequent lymph node involvement and a poor prognosis. CCS is also referred as a malignant melanoma of soft parts because of its melanocytic f
7#
發(fā)表于 2025-3-22 19:00:29 | 只看該作者
Epithelioid Sarcoma,btypes of ES have been delineated, proximal and distal types, correlating with distinct clinical presentations. ES display diffuse keratin expression, an unusual feature in mesenchymal tumor and have a loss of SMARCB1 protein expression. Clinically, ES appears as a firm nodule, often accompanied by
8#
發(fā)表于 2025-3-22 23:47:24 | 只看該作者
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發(fā)表于 2025-3-23 01:59:08 | 只看該作者
Desmoplastic Small Round Cell Tumors,ales characterized by a specific translocation t(11:22)(p13;q12), which fuses the ESWR1 gene to the WT1 gene. The estimated incidence ranges between 0.2 and 0.7 cases per million per year. DSRCT has an extremely aggressive clinical course, most patients having distant metastases at diagnosis, either
10#
發(fā)表于 2025-3-23 06:41:31 | 只看該作者
Solitary Fibrous Tumours,y occur in middle-aged adult aged 20–70?years. Most tumours are well-delineated slow growing mass while some malignant tumours are more infiltrative. On microscopy, typical SFT show a patternless architecture with a combination of hypocellular and hypercellular areas. The hypercellular areas contain
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