RESUMEN
Anaplastic sarcoma of kidney (ASK) is a rare neoplasm recently associated with DICER1 mutations. We report a child with germline DICER1 mutation who developed ASK in preexisting septated renal cysts, which were likely cystic nephroma. From age 2.5 to 6 years, sonographic imaging illustrated changes in the size and number of renal cysts, followed at age 8.8 years by a mass, pathologically an ASK. Lung cysts resected in infancy were diagnosed retrospectively as pleuropulmonary blastoma. Both tumors had acquired somatic DICER1 mutations. Ultrasonographic evolution of renal cysts to ASK has not previously been documented. Children with both pulmonary and renal cysts are candidates for DICER1 mutation testing.
Asunto(s)
Quistes , ARN Helicasas DEAD-box/genética , Enfermedades Genéticas Congénitas , Neoplasias Renales , Blastoma Pulmonar , Ribonucleasa III/genética , Sarcoma , Niño , Preescolar , Quistes/genética , Quistes/patología , Quistes/cirugía , Femenino , Enfermedades Genéticas Congénitas/genética , Enfermedades Genéticas Congénitas/patología , Enfermedades Genéticas Congénitas/cirugía , Humanos , Lactante , Neoplasias Renales/genética , Neoplasias Renales/patología , Neoplasias Renales/cirugía , Blastoma Pulmonar/genética , Blastoma Pulmonar/patología , Blastoma Pulmonar/cirugía , Sarcoma/genética , Sarcoma/patología , Sarcoma/cirugía , SíndromeRESUMEN
This is an 11-year survey of molecular analysis of APC germline mutations for the province of Quebec done at the Molecular Pathology Unit of the Jewish General Hospital which offers genetic testing for hereditary forms of colorectal cancer for the whole of Quebec province. We report on 47 unique mutations seen in 66 families affected with familial adenomatous polyposis. Of these unique mutations, 60% are short indels, 28% are point mutations, and 6% are whole exon deletions. The absence of founder mutations and the variety of mutations encountered reinforce the value of RNA-based testing and the need for gene dosage techniques such as multiplex ligation-dependent probe amplification.