Wilms' Tumor in the Adult — Report of a Case and Review of the Literature
Autor: | Jacob Briner, Jean-Pierre Droz, Arnaud D. Roth, Ayman Tawil, Sami Remadi, Jeremiah N. Cox |
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Rok vydání: | 1999 |
Předmět: |
Male
medicine.medical_specialty Genes Wilms Tumor Lung Neoplasms Adolescent medicine.medical_treatment Postoperative radiotherapy Wilms Tumor Nephrectomy Pathology and Forensic Medicine Immunoenzyme Techniques Genes Wilms Tumor/genetics Antineoplastic Combined Chemotherapy Protocols Tumor stage Biomarkers Tumor medicine Humans Combined Modality Therapy Grading (tumors) Neoplasm Staging Wilms Tumor/chemistry/genetics/secondary/therapy ddc:616 Chemotherapy Tumor Markers Biological/analysis ddc:617 business.industry Wilms' tumor Cell Biology medicine.disease Kidney Neoplasms Surgery Radiation therapy Karyotyping Kidney Neoplasms/chemistry/genetics/pathology/therapy Lung Neoplasms/secondary/therapy Antineoplastic Combined Chemotherapy Protocols/therapeutic use Radiology Tomography X-Ray Computed business |
Zdroj: | Pathology-Research and Practice, Vol. 195, No 2 (1999) pp. 105-11;discussion113-4 |
ISSN: | 0344-0338 |
Popis: | Wilms' tumor is rare in adults. Its histology, grading and staging are identical to those in children. Investigators agree on a combined modality approach in the treatment of adult Wilms' tumor (AWT), but differ on how aggressive it should be. Some advocate adopting the current pediatric protocols which take into account tumor stage and grade. Others recommend using advanced disease regimens for all stages and grades. We report on an 18 year-old male with stage IV favorable histology Wilms' tumor. The patient underwent radical nephrectomy and received postoperative radiotherapy with intensive four-drug chemotherapy. He had one relapse after 12 months which was successfully treated with chemotherapy and radiotherapy. He remains in remission without relapses 36 months after the initial diagnosis. The genetics of Wilms' tumor has been well studied in children but is practically unknown in adults; karyotype and molecular genetic studies in this case were normal. |
Databáze: | OpenAIRE |
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