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[Case report of rare co-occurrence of renal cell carcinoma and crossed renal dystopia (L-shaped kidney)].
Bakov, V N; Los, M S.
Afiliação
  • Bakov VN; Regional Clinical Hospital, Yaroslavl, Russia.
  • Los MS; Regional Clinical Hospital, Yaroslavl, Russia.
Urologiia ; (5): 96-99, 2017 Oct.
Article em Ru | MEDLINE | ID: mdl-29135151
ABSTRACT
L-shaped kidney refers to a rare anomaly of the relative kidney positioning. Due to low prevalence, the literature on the co-occurrence of this anomaly with malignancy is lacking. And, if the diagnosis of a renal anomaly does not present difficulties, if a tumor is detected in such a kidney, even MSCT does not always help differentiate a pelvic tumor from a tumor of the renal parenchyma spreading to the pelvicalyceal system. This has important implications for choosing an appropriate surgical strategy. A feature of the presented clinical observation is the co-occurrence of the rare anomaly of kidney position and locally advanced renal cell carcinoma spreading to the renal pelvis. Due to the massive spread of the tumor, an organ-sparing surgery was not feasible. Due to the suspicion of tumor spread to the renal pelvis, the patient underwent nephrureterectomy of the L-shaped kidney. Introduction to renoprival state with transfer to chronic hemodialysis became the only option to maintain homeostasis and extend the patients life. Histological examination revealed clear cell renal cell carcinoma with invasion of the pelvis and renal capsule, with no clear demarcation between the fused kidneys.
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Rim / Neoplasias Renais / Nefrectomia Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Middle aged Idioma: Ru Ano de publicação: 2017 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Rim / Neoplasias Renais / Nefrectomia Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Middle aged Idioma: Ru Ano de publicação: 2017 Tipo de documento: Article