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Gaceta medica de Mexico, 1971 Some of the next articles are maybe not open access.
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Scottish Medical Journal, 1971
The results of treatment of 45 patients with nephroblastoma in the period 1953–1968 are presented. The overall three year survival rate is 27% while for those given radiotherapy and repeated courses of Actinomycin D following operation the three year survival rate is 40%. The results reported from other centres are discussed.
G F, Milligan, D G, Young
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The results of treatment of 45 patients with nephroblastoma in the period 1953–1968 are presented. The overall three year survival rate is 27% while for those given radiotherapy and repeated courses of Actinomycin D following operation the three year survival rate is 40%. The results reported from other centres are discussed.
G F, Milligan, D G, Young
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Journal of Urology, 1984
Nephroblastoma, or Wilms tumor, is the most common renal neoplasm in children and accounts for approximately a fifth of all malignant growths in this age group. However, the incidence of Wilms tumor in adults is much less common, with less than 200 cases having been reported in the literature.
D R, Roth +3 more
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Nephroblastoma, or Wilms tumor, is the most common renal neoplasm in children and accounts for approximately a fifth of all malignant growths in this age group. However, the incidence of Wilms tumor in adults is much less common, with less than 200 cases having been reported in the literature.
D R, Roth +3 more
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British Journal of Urology, 1964
SUMMARY A case of unattached nephroblastoma in a boy of 2 years of age is presented with comments. We wish to express our grateful thanks to Mr Kamalanathan, Mrs Sunila Bhajekar, and the Norman Institute of Pathology for their help.
A B, BHAJEKAR, M, JOSEPH, H S, BHAT
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SUMMARY A case of unattached nephroblastoma in a boy of 2 years of age is presented with comments. We wish to express our grateful thanks to Mr Kamalanathan, Mrs Sunila Bhajekar, and the Norman Institute of Pathology for their help.
A B, BHAJEKAR, M, JOSEPH, H S, BHAT
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Virchows Archiv Fur Pathologische Anatomie Und Physiologie Und Fur Klinische Medizin, 1984
A case of an extrarenal nephroblastoma is reported which was located in the inguinal region. In the surrounding fat tissue normal ectopic glomerular and tubular structures and two more nephroblastomas were found. Therefore and because of negative clinical investigations in regarding of a renal malignant tumour the inguinal mass was thought to be the ...
H, Lüchtrath +3 more
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A case of an extrarenal nephroblastoma is reported which was located in the inguinal region. In the surrounding fat tissue normal ectopic glomerular and tubular structures and two more nephroblastomas were found. Therefore and because of negative clinical investigations in regarding of a renal malignant tumour the inguinal mass was thought to be the ...
H, Lüchtrath +3 more
exaly +3 more sources
Scandinavian Journal of Urology and Nephrology, 1977
A case of adult nephroblastoma in a 51-year-old woman is reported. A percutaneous aspiration biopsy did not lead to the right diagnosis presumably because the histologic structure of the tumour consisted exclusively of more or less differentiated epithelial-like elements, while mesenchymal tumour components were not demonstrated.
D, Francis, N J, Olsen
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A case of adult nephroblastoma in a 51-year-old woman is reported. A percutaneous aspiration biopsy did not lead to the right diagnosis presumably because the histologic structure of the tumour consisted exclusively of more or less differentiated epithelial-like elements, while mesenchymal tumour components were not demonstrated.
D, Francis, N J, Olsen
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Ryoikibetsu shokogun shirizu, 1997
Effective diagnosis, staging, and multimodality therapies dramatically decreased the morbidity and mortality of children with Wilms Tumor. Increasing awareness of the disease, biology, genetics, and epidemiology improved assessment of clinical syndromes and led to more risk-based treatment.
G M, Haase, M L, Ritchey
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Effective diagnosis, staging, and multimodality therapies dramatically decreased the morbidity and mortality of children with Wilms Tumor. Increasing awareness of the disease, biology, genetics, and epidemiology improved assessment of clinical syndromes and led to more risk-based treatment.
G M, Haase, M L, Ritchey
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Journal of Cancer Research and Clinical Oncology, 1989
The cases of extrarenal nephroblastoma published in the world literature have been tabulated and reviewed, and are discussed from a historical point of view.
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The cases of extrarenal nephroblastoma published in the world literature have been tabulated and reviewed, and are discussed from a historical point of view.
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