Multiple primary malignancies and subtle mucocutaneous lesions associated with a novel PTEN gene mutation in a patient with Cowden syndrome: Case report

Autor: Křepelová Anna, Hatlová Jana, Šenkeříková Mária, Vasovčák Peter
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Zdroj: BMC Medical Genetics, Vol 12, Iss 1, p 38 (2011)
Druh dokumentu: article
ISSN: 1471-2350
DOI: 10.1186/1471-2350-12-38
Popis: Abstract Background Cowden syndrome (CS) is a cancer predisposition syndrome associated with increased risk of breast, thyroid, and endometrial cancers, and is characterized by development of benign mucocutaneous lesions. Case presentation Here we report on a 58-year-old woman with multiple primary malignancies and subtle mucocutaneous lesions such as small polyps and wart-like papulas. Over a period of 23 years, she developed various malignant neoplasms including thyroid, ovarian, stomach, and colon carcinomas, and a benign meningioma. Direct sequencing analysis of the PTEN gene revealed a novel germline mutation (c.438delT, p.Leu146X). Conclusion This case demonstrates that Cowden syndrome is a multi-system disease that can result in the development of multiple malignant and benign tumors.
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