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Titlebook: Carcinoma of the Kidney and Testis, and Rare Urologic Malignancies; Innovations in Manag Zbigniew Petrovich (Professor of Radiation Oncolog

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發(fā)表于 2025-3-21 17:17:08 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Carcinoma of the Kidney and Testis, and Rare Urologic Malignancies
副標題Innovations in Manag
編輯Zbigniew Petrovich (Professor of Radiation Oncolog
視頻videohttp://file.papertrans.cn/222/221704/221704.mp4
概述the book provides current information on the etiology, diagnosis and treatment - well referenced, comprehensive update on the topics presented - provides good assistance to teaching - numerous illustr
叢書名稱Medical Radiology
圖書封面Titlebook: Carcinoma of the Kidney and Testis, and Rare Urologic Malignancies; Innovations in Manag Zbigniew Petrovich (Professor of Radiation Oncolog
描述In the United States in 1997, 28800 new cases of malignant tumors of the kidney and renal pelvis were diagnosed along with 2100 new cases of malignant tumors of the ureter and other urinary organs, 7200 primary malignant tumors of the testis, and 1300 primary malignant tumors of the penis and other genital organs. In large measure, surgery is the treatment of choice for these tumors, but radiation therapy is in- creasingly recognized as having significant and important curative and palliative bene- fits in each of these tumor sites. Surgery is the standard form of treatment for non- metastatic renal cell carcinomas as well as for malignancies of the renal pelvis and ureter, with radical nephrectomy and radical uretectomy being employed. However, postoperative radiation therapy is of value for those patients who demonstrate evi- dence of residual tumor following surgery, transection of tumor during surgery, or positive regional lymph node drainage. As regards the rare tumors that involve the female urethra, surgical resection is appropriate for those that are limited and local in character and amenable to partial ureterectomy. With tumors that are more advanced in character, however
出版日期Book 1999
關(guān)鍵詞Karzinom; Tumor; cancer; carcinoma; cell; diagnosis; fertility; genetics; imaging; kidney; molecular genetics;
版次1
doihttps://doi.org/10.1007/978-3-642-59839-5
isbn_softcover978-3-642-64144-2
isbn_ebook978-3-642-59839-5Series ISSN 0942-5373 Series E-ISSN 2197-4187
issn_series 0942-5373
copyrightSpringer-Verlag Berlin Heidelberg 1999
The information of publication is updating

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Imaging of Renal Parenchymal Tumorsons. Therefore, optimization of the imaging techniques is a continuous challenge for radiologists. Once a renal mass is detected, the radiologist is faced with two additional tasks: (1) to determine whether it is a simple renal cyst/benign lesion or a malignant tumor, or more simply, whether or not
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Nephron-Sparing Surgerycancer, the mortality from kidney cancer can be estimated to be twice as high as that from bladder and 3 times as high as that from prostate cancer. The clinical picture of renal cell carcinoma has, however, changed completely during the last decade. Most tumors are no longer presenting at a locally
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Palliative Surgical Therapyetastatic disease at presentation. Following nephrectomy for apparently localized disease, 50% of patients will develop progression with the occurrence of distant metastases or locoregional recurrence. Most of these patients die within 1 year and the reported 5-year survival rates vary between 0% an
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Immunotherapy and Chemotherapy for Metastatic Renal Cell Carcinomanosis (. et al. 1997). For these patients the prognosis is poor, with an estimated median survival of less than 1 year and an overall 5-year survival of less than 20% (. et al. 1991). Spontaneous remissions of metastatic lesions have on rare occasions been documented to occur after removal of the pr
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The Role of Radiotherapy in the Management of Patients with Renal Cell Carcinomaf all genitourinary tumors in incidence and 18% in mortality rates (. et al. 1998). Most (>80%) tumors of the kidneys are renal cell carcinomas (RCCs), which show a predilection to occur in males in their fifth and sixth decades of life, although this tumor is known to occur in much younger patients
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