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Volume 195, Issue 1, Pages 75-79 (November 2009)


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Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast–ovarian cancer syndromes: a case report

Laura Papia, Domenico Pallib, Laura Masic, Anna Laura Putignanoa, Caterina Congregatia, Ines Zannab, Francesca Marinic, Francesca Giustic, Ettore Luzic, Francesco Tonellid, Maurizio Genuardia, Maria Luisa BrandiceCorresponding Author Informationemail address, Alberto Falchettic

Received 4 May 2009; received in revised form 17 June 2009; accepted 20 June 2009.

Abstract 

The simultaneous occurrence of mutations in two different tumor suppressor genes in the same individual is a very rare event. Here we report the case of a woman in whom germline mutations in both MEN1 and BRCA1 were identified. The severity of MEN1-related biochemical and clinical findings did not significantly differ from that for other affected family members lacking the BRCA1 mutation, except for the development of an extremely large visceral lipoma; the proband has not developed any BRCA1-related malignancies. We explore genetic and molecular rationales for an association between these neoplastic processes.

a Medical Genetics Unit, Department of Clinical Pathophysiology, University of Florence, Florence, Italy

b Molecular and Nutritional Epidemiology Unit, Cancer Research and Prevention Institute (ISPO), Florence, Italy

c Regional Centre for Hereditary Endocrine Tumors, Unit of Metabolic Bone Diseases, Department of Internal Medicine, University of Florence, Viale Morgagni, 85, 50135 Florence, Italy

d Unit of Surgery, Department of Clinical Pathophysiology, University of Florence, Florence, Italy

e Spin-off DeGene, Florence, Italy

Corresponding Author InformationCorresponding author. Tel.: +39-055-4296586; fax: +39-055-4296585.

PII: S0165-4608(09)00335-5

doi:10.1016/j.cancergencyto.2009.06.019


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