Résumé
Twenty-eight cases of transitional cell carcinomas, (19 papillary cell carcinomas, 9 nonpapillary invasive carcinomas) with concomitant mucosal biopses are reported. Multiple biopses were obtained cystoscopically at diagnosis (during ressection or biopsy of the main tumor) or afterwards, during post-operative evaluation. Fifteen patients (53.6%) wre positive for dysplasia, carcinoma "in situ" or micro-invasive carcinoma in the biopsies. These lesions were correlated with the primary neoplasm in regard to: 1) histological grade. Atypical lesions were more frequent the higher the grade (0.01 < p < 0.05); 2) clinical staging. The possibility of finding atypical lesions was higher in cases with more advanced staging (0.01 < < 0.05) and 3) presence of one or more tumors visible cystoscopically. The results were not statistically significant (0.10 < p < 0.50) but there was a trend toward a highr incidence of atypical lesions among patients with more than one tumor at cystoscopy. Performance of multiple mucosal biopsies is the only means of diagnosing for atypical lesions of the bladder because, due to their plane configuration, they are not detected cystoscopically. The presence of these lesions is very important because they influence the prognosis and the therapeutic measures
Sujets)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Tumeurs de la vessie urinaire/anatomopathologie , Carcinome transitionnel/anatomopathologie , Biopsie , Études rétrospectives , Cystoscopie , Stadification tumoraleRésumé
Os autores relatam caso de um paciente que apresentou síndrome nefrótica quatro anos após o diagnóstico de leucemia mielóide crônica. A biópsia renal revelou lesöes características da glomerulopatia membranosa. Acreditamos que este represente o primeiro caso relatado na literatura da associaçäo entre leucemia mielóide crônica e glomerulopatia membranosa
Sujets)
Humains , Adulte d'âge moyen , Mâle , Glomérulonéphrite extra-membraneuse/complications , Leucémie myéloïde chronique BCR-ABL positive/complications , Syndrome néphrotique/étiologie , Busulfan/usage thérapeutique , Glomérulonéphrite extra-membraneuse/traitement médicamenteux , Glomérulonéphrite extra-membraneuse/anatomopathologie , Leucémie myéloïde chronique BCR-ABL positive/diagnostic , Leucémie myéloïde chronique BCR-ABL positive/anatomopathologie , Leucémie myéloïde chronique BCR-ABL positive/traitement médicamenteux , Syndrome néphrotique/diagnostic , Syndrome néphrotique/anatomopathologie , Syndrome néphrotique/traitement médicamenteuxRésumé
Os autores relatam um caso de granulomatose de Wegener com insuficiência renal rapidamente progressiva que evoluiu para óbito. Os achados histopatológicos evidenciaram glomerulonefrite granulomatosa e necrose papilar renal, achados estes pouco freqüentes na moléstia. Discutem-se os diagnósticos diferenciais da granulomatose de Wegener