先天性精阜肥大症の1治験例
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概要
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A 9-year-old boy was admitted to the hospital w i th the chief complaint of pollakisuria and nykturia. B i lateral hydronephrosis and dilatation of the bladder were revealed roentgenologically. The hypertrophied verumontanum was observed and resected opera t i vely, but no other congenital abnormalities were found. Histological section showed that it consisted of connective tissue covered by a thin layer of transitional epithelium. The patient i s doing well postoperatively and the results of treatment are satisfactory. Literature of congenital hypertrophy of verumontanum was reviewed.
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