Sarcomatoid carcinoma of the kidney in a MEN1 patient: case report and genetic profile.
Endocr J
; 61(8): 781-7, 2014.
Article
em En
| MEDLINE
| ID: mdl-24882518
Renal tumors are exceedingly rare in Multiple Endocrine Neoplasia type 1 (MEN1), a pleyotropic hereditary cancer disorder affecting the endocrine system. Herein we report a unique case of renal sarcomatoid carcinoma with concomitant ipsilateral non-secreting adrenal adenoma occurring in a young male MEN1 patient, previously operated for hyperparathyroidism and multiple pancreatic neuroendocrine neoplasms. Molecular analysis in the MEN1 locus at 11q13 showed loss of heterozygosity in the adrenal lesion, while kidney cancer was unrelated to MEN1 syndrome.
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Base de dados:
MEDLINE
Assunto principal:
Carcinoma de Células Renais
/
Proteínas Proto-Oncogênicas
/
Neoplasia Endócrina Múltipla Tipo 1
/
Neoplasias Renais
Idioma:
En
Ano de publicação:
2014
Tipo de documento:
Article