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Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report
Article de En | WPRIM | ID: wpr-210098
Bibliothèque responsable: WPRO
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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Texte intégral: 1 Indice: WPRIM Sujet Principal: Pedigree / Polykystose rénale autosomique dominante / Radiopharmaceutiques / Succimer de technétium (99mTc) / Abdomen / Rein Limites du sujet: Aged / Female / Humans / Male langue: En Texte intégral: Journal of Korean Medical Science Année: 2003 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pedigree / Polykystose rénale autosomique dominante / Radiopharmaceutiques / Succimer de technétium (99mTc) / Abdomen / Rein Limites du sujet: Aged / Female / Humans / Male langue: En Texte intégral: Journal of Korean Medical Science Année: 2003 Type: Article