Multifocal Renal Cell Carcinoma of Different Histological Subtypes in Autosomal Dominant Polycystic Kidney Disease
Korean Journal of Pathology
; : 382-386, 2012.
Article
de En
| WPRIM
| ID: wpr-32984
Bibliothèque responsable:
WPRO
ABSTRACT
Renal cell carcinoma (RCC) in autosomal dominant polycystic kidney (ADPKD) is rare. To date, 54 cases of RCC in ADPKD have been reported. Among these, only 2 cases have different histologic types of RCC. Here we describe a 45-year-old man who received radical nephrectomy for multifocal RCC with synchronous papillary and clear cell histology in ADPKD and chronic renal failure under regular hemodialysis. The case reported herein is another example of the rare pathological finding of RCC arising in a patient with ADPKD.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Néphrocarcinome
/
Dialyse rénale
/
Polykystose rénale autosomique dominante
/
Défaillance rénale chronique
/
Néphrectomie
Limites du sujet:
Humans
langue:
En
Texte intégral:
Korean Journal of Pathology
Année:
2012
Type:
Article