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Titlebook: Renal and Adrenal Tumors; Pathology, Radiology Eberhard Löhr,Lutz-Dietrich Leder Book 1987Latest edition Springer-Verlag Berlin Heidelberg

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,Prenatal Wilms’ Tumor,onishing “inborn” tumors was written by W. [50] who gathered 255 observations. Although this important paper touches a very interesting biologic problem, it has not yet received much interest. Influenced by our own six cases of newborns with neuroblastoma and three newborns with Wilms’ tumors, B. tr
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Congenital Neuroblastoma, years of age [9]. Although its appearance is scattered throughout childhood, diagnosis is made within the first 12 months of life in one-third of patients and in the 2nd and 3rd years of life in another one-third (Fig. 1).
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,Nonsurgical Management of Wilms’ Tumor,est cure rates of all malignancies in children. Even with the presence of metastases at the time of diagnosis, or in the case of bilateral Wilms’ tumor, promising therapeutic regimens have been reported [39, 7, 4]. Advances in treatment in the past decade have also improved the survival rate for pat
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Immunologic Aspects of Malignant Renal Disease,ccasional spontaneous regression of metastases, their erratic growth, or their occasional late occurrence following nephrectomy were thought to be strong clinical arguments for this assumption. L. et al. (1959), reporting on a case of histologically proven spontaneous regression of lung metastases,
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,Prenatal Wilms’ Tumor,em, it has not yet received much interest. Influenced by our own six cases of newborns with neuroblastoma and three newborns with Wilms’ tumors, B. tried — utilizing the cases described in the literature — to crystallize the general trend of this disease by analyzing its course in individuals.
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eworked second edition that includes the modern advances in this field. There has been a complete change of diagnostic procedure in the detection of renal tumors, which is now based on sonography, computed tomography, and nuclear magnetic resonance imaging, pushing intravenous urography and angiogra
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