Cavalli Tiziana, Giudici Francesco, Nesi Gabriella, Marini Francesca, Giusti Francesca, Cavalli Loredana, Brandi Maria Luisa, Tonelli Francesco
Department of Surgery and Translational Medicine, University of Florence, Florence, Italy.
Endocr J. 2014;61(8):781-7. doi: 10.1507/endocrj.ej14-0021. Epub 2014 May 30.
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.