| Literature DB >> 24882518 |
Tiziana Cavalli1, Francesco Giudici, Gabriella Nesi, Francesca Marini, Francesca Giusti, Loredana Cavalli, Maria Luisa Brandi, Francesco Tonelli.
Abstract
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.Entities:
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Year: 2014 PMID: 24882518 DOI: 10.1507/endocrj.ej14-0021
Source DB: PubMed Journal: Endocr J ISSN: 0918-8959 Impact factor: 2.349