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Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report
Journal of Korean Medical Science ; : 284-286, 2003.
Artículo en Inglés | WPRIM | ID: wpr-210098
ABSTRACT
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.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Linaje / Riñón Poliquístico Autosómico Dominante / Radiofármacos / Ácido Dimercaptosuccínico de Tecnecio Tc 99m / Abdomen / Riñón Límite: Anciano / Femenino / Humanos / Masculino Idioma: Inglés Revista: Journal of Korean Medical Science Año: 2003 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Linaje / Riñón Poliquístico Autosómico Dominante / Radiofármacos / Ácido Dimercaptosuccínico de Tecnecio Tc 99m / Abdomen / Riñón Límite: Anciano / Femenino / Humanos / Masculino Idioma: Inglés Revista: Journal of Korean Medical Science Año: 2003 Tipo del documento: Artículo