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Titlebook: Bone and Soft Tissue Tumors; Clinical Features, I Mario Campanacci Book 1999Latest edition Springer-Verlag Wien 1999 Carcinom.Staging.Tumor

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發(fā)表于 2025-3-21 16:30:34 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Bone and Soft Tissue Tumors
期刊簡(jiǎn)稱Clinical Features, I
影響因子2023Mario Campanacci
視頻videohttp://file.papertrans.cn/190/189732/189732.mp4
發(fā)行地址First edition sold within 2 years.Concise description of each pathologic entity, based on personal experience and literature.Clinical aspects, imaging, pathology, and treatment are equally balanced.Ne
圖書封面Titlebook: Bone and Soft Tissue Tumors; Clinical Features, I Mario Campanacci Book 1999Latest edition Springer-Verlag Wien 1999 Carcinom.Staging.Tumor
影響因子to the first edition (1990) This is an extraordinary book by an extraordinary author. Mario Campanacci first pub- lished three volumes on musculoskeletal neoplasms and other tumor-like processes in bone and soft parts in Italian in 1981-1985. This book is an update and expansion of that book, published for the first time in English. In this book Dr. Campanacci brings to the readers the vast experience in musculoskeletal oncology of the Rizzoli Orthopaedic Institute in Bologna where he has been head of the Oncology Unit for many years. As such, he has had at his dis- posal the patient records, radiographs and pathologic material dating back to 1905. In fact, a visitor to the Institute will be shown the radiograph made of the first tumor case on record- that of a giant cell tumor of the distal femur. The wealth of clinical material that has been ac- cumulated at the Rizzoli Institute, with exquisite documentation and maintenance is a unique resource and testimonial to not only the author but his predecessors. Under Campanacci‘ s leadership, the Institute has provided care to the majority of patients with neoplasms through- out Italy. Over the past two decades a treatment team with ex
Pindex Book 1999Latest edition
The information of publication is updating

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發(fā)表于 2025-3-21 20:19:53 | 只看該作者
Writers as Progenitors and Offspring as a benign tumor, but has a significant tendency to recur locally and, rarely, may produce pulmonary metastases. These have the same histological features as the primary tumor and are frequently curable. Rarely, a giant cell tumor may transform into a high-grade sarcoma.
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the author but his predecessors. Under Campanacci‘ s leadership, the Institute has provided care to the majority of patients with neoplasms through- out Italy. Over the past two decades a treatment team with ex978-3-7091-3846-5
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發(fā)表于 2025-3-23 00:31:55 | 只看該作者
Giant Cell Tumors and osteoclast-like multi-nucleated giant cells, and having a variable and unpredictable potential for growth.. The giant cell tumor usually behaves as a benign tumor, but has a significant tendency to recur locally and, rarely, may produce pulmonary metastases. These have the same histological fe
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發(fā)表于 2025-3-23 03:09:20 | 只看該作者
Multiple Chondromasy. When the chondromas are more extensively distributed, the term of . is also employed. Multiple chondromas associated with soft tissues hemangiomas are known as . Extensive multiple chondromas cause shortening and deformity of the affected bones, and undergo a frequent transformation into a chondr
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發(fā)表于 2025-3-23 07:57:31 | 只看該作者
https://doi.org/10.1007/978-3-7091-3846-5Carcinom; Staging; Tumor; classification; electron microscopy; orthopaedics; surgery; surgical oncology; Rad
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