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Titlebook: Atlas of Musculoskeletal Tumors and Tumorlike Lesions; The Rizzoli Case Arc Piero Picci,Marco Manfrini,Daniel Vanel Book 20141st edition Sp

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发表于 2025-3-21 17:46:27 | 显示全部楼层 |阅读模式
期刊全称Atlas of Musculoskeletal Tumors and Tumorlike Lesions
期刊简称The Rizzoli Case Arc
影响因子2023Piero Picci,Marco Manfrini,Daniel Vanel
视频videohttp://file.papertrans.cn/165/164355/164355.mp4
发行地址Covers a wide range of lesions from a multidisciplinary perspective, highlighting clinical, radiological, and histological correlations.Reports treatment for each entity.Analyzes biomolecular findings
图书封面Titlebook: Atlas of Musculoskeletal Tumors and Tumorlike Lesions; The Rizzoli Case Arc Piero Picci,Marco Manfrini,Daniel Vanel Book 20141st edition Sp
影响因子This book reflects the experience of the Rizzoli Orthopedic Institute during more than 100 years of treatment of musculoskeletal tumor and tumorlike lesions. It presents a wide range of lesions from a multidisciplinary perspective, highlighting pertinent clinical, radiological, and histological correlations. Treatment is briefly reported for each entity. In addition, the more recent biomolecular findings of use for diagnosis, prognosis, and treatment are carefully analyzed. The Rizzoli case archive spans more than a century, the first treated case dating back to 28 September 1900, and contains the original material – clinical charts, imaging, paraffin blocks, and histological slides – of more than 40,000 cases, including about 29,000 bone lesions and 11,000 soft tissue lesions. This book reports the most relevant entities and reflects the improvements in knowledge of musculoskeletal tumors as presented during the yearly international course held at the Rizzoli Institute.​  
Pindex Book 20141st edition
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Classification of Primary Bone Tumorsin general to a growing mass and is also used by clinicians for lesions of nonneoplastic nature, such as histiocytic fibroma and osteochondroma, because their basic tissue expresses a recognizable differentiation, such as fibrohistiocytic and cartilaginous. Other growing lesions are usually defined
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Multiple Chondromas (Chondromatosis, Ollier’s Disease) Associated Condition: Maffucci’s Syndromeeir distribution and spectrum of presentation is variable. Only few chondromas are limited to the hands or one limb with minimal if any symptoms or, in other cases, diffusion is hemisomic, or extended to the entire body with hemisomic prevalence and overall features of diffuse chondrodysplasia, know
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Multiple Exostosesr as compared to solitary osteochondroma. Heredity is present in 2/3 of cases. Transmission is autosomal dominant. Basic research has identified several genetic abnormalities determining the disease. Most common mutations involve gene EXT1 on chromosome 8 and gene EXT2 on chromosome 11; a third gene
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Piero Picci,Marco Manfrini,Daniel VanelCovers a wide range of lesions from a multidisciplinary perspective, highlighting clinical, radiological, and histological correlations.Reports treatment for each entity.Analyzes biomolecular findings
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