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Journal of Korean Medical Science ; : 284-286, 2003.
Artículo en Inglés | WPRIM | ID: wpr-210098

RESUMEN

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases of unilateral ADPKD with agenesis of contralateral kidney have been reported. We present a case of unilateral ADPKD with agenesis of contralateral kidney in a 66-yr-old man. Radiographic images showed the enlarged right kidney with multiple variable-sized cysts and the absence of the left kidney. The diagnosis of ADPKD was confirmed by the family screening. The patient received maintenance hemodialysis for endstage renal disease. We report a case of unilateral ADPKD associated with contralateral renal agenesis in a 66-yr-old male patient with a literature review.


Asunto(s)
Anciano , Femenino , Humanos , Masculino , Abdomen/patología , Riñón/anomalías , Linaje , Riñón Poliquístico Autosómico Dominante/diagnóstico , Riñón Poliquístico Autosómico Dominante/patología , Riñón Poliquístico Autosómico Dominante/fisiopatología , Radiofármacos/metabolismo , Ácido Dimercaptosuccínico de Tecnecio Tc 99m/metabolismo
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