Breast cancer as part of Cowden syndrome
https://doi.org/10.18027/2224-5057-2022-12-2-36-44
Abstract
Cowden syndrome is a rare disease characterized by multiple hamartomas and increased breast, thyroid, kidney and uterine neoplasm risk. The lifetime breast cancer risk for patients with Cowden syndrome is 85 %, with an average age of diagnosis between 38 and 46 years. The diagnostic criteria for Cowden syndrome have been established by the International Cowden Consortium (ICC) and the National Comprehensive Cancer Network (NCCN), and are regularly revised, but the diagnosis of Cowden syndrome remains difficult due to the variety of phenotypic and clinical features of the disease. At the same time, the genetic variants associated with Cowden syndrome analysis is not a standard for patients with breast cancer.
Objective: To demonstrate the non‑BRCA hereditary breast cancer detection using whole genome sequencing on the Cowden syndrome clinical case example.
Materials and methods: The article describes a clinical case of a 37‑year‑old female patient with breast cancer, normal intelligence and phenotype, structural abnormalities of the thyroid gland (multinodular goiter). Whole genome sequencing was used to identify clinically significant genetic variants associated with hereditary tumor syndromes.
Clinical case: The article presents a brief literature review on the clinical presentation of Cowden syndrome and indications for its molecular diagnosis. Also, the presented clinical case describes patient R., 37 years old female with breast cancer, who underwent treatment in the City Clinical Oncological Hospital № 1 of the Moscow City Health Department in 2021. The patient was fully examined and enrolled in the whole genome sequencing project under the Order № 69 of Moscow Healthcare Department dated February 1, 2021 «Oncogenetic research organization in Moscow». The results revealed a pathogenic variant in the PTEN gene, previously associated with Cowden syndrome.
Conclusion: The use of whole genome sequencing allows to identify hereditary tumor syndromes, the clinical manifestation of which may be breast cancer.
About the Authors
M. M. ByakhovaRussian Federation
Mariya M. Byakhova, MD, PhD, Head of the Genetics Laboratory, Center for Pathological Anatomical Diagnostics and Molecular Genetics
Moscow
A. B. Semenova
Russian Federation
Anna B. Semenova, MD, PhD, DSc, Head of the Center for Pathological Diagnosis and Molecular Genetics
Moscow
V. N. Galkin
Russian Federation
Vsevolod N. Galkin, MD, PhD, DSc, Professor, Chief of Medicine
Moscow
C. V. Homushku
Russian Federation
Chinchi V. Homushku, Laboratory Geneticist, Genetics Laboratory, Center for Pathological Diagnosis and Molecular Genetics
Moscow
A. E. Zod»binova
Russian Federation
Aisa E. Zod»binova, Laboratory Geneticist, Genetics Laboratory, Center for Pathological Diagnosis and Molecular Genetics
Moscow
M. V. Makarova
Russian Federation
Maria V. Makarova, Geneticist, Oncologist, Head of Oncology Genetics
Moscow
E. E. Baranova
Russian Federation
Elena E. Baranova, MD, PhD, Geneticist, Medical Director of Evogen LLC, Associate Professor of the Department of Medical Genetics
Moscow
O. V. Sagaydak
Russian Federation
Olesya V. Sagaydak, MD, PhD, Head of the Scientific and Medical Department
Moscow
D. K. Chernevskiy
Russian Federation
Denis K. Chernevsky, Clinical Sequencing Expert
Moscow
M. S. Belenikin
Russian Federation
Maxim S. Belenikin, MD, PhD сhemistry, Head of the Laboratory and Director for Science and Development
Moscow
A. A. Krinitsina
Russian Federation
Anastasia A. Krinitsyna, MD, PhD biol., Deputy Head of the Laboratory
Moscow
M. V. Vorontsova
Russian Federation
Maria V. Vorontsova, MD, PhD, Pediatric Endocrinologist, Leading Researcher, Department of Pediatric Thyroidology, Reproductive and Somatic Development
Moscow
N. A. Bodunova
Russian Federation
Natalya A. Bodunova, MD, PhD, Gastroenterologist, Head of the Center for Personalized Medicine
Moscow
A. M. Danishevich
Russian Federation
Anastasia M. Danishevich, Geneticist, Center for Personalized Medicine
Moscow
I. E. Khatkov
Russian Federation
Igor E. Khatkov, MD, PhD, DSc, Corresponding Member of the Russian Academy of Sciences, Director; Chief Freelance Specialist‑Oncologist of the Moscow Department of Health, Head of the Department of Faculty Surgery, Medical Faculty of the Moscow State University of Medicine and Dentistry
Moscow
D. A. Degterev
Russian Federation
Moscow
T. I. Yanova
Russian Federation
Tatiana I. Yanova, Geneticist
Moscow
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Review
For citations:
Byakhova M.M., Semenova A.B., Galkin V.N., Homushku C.V., Zod»binova A. ., Makarova M.V., Baranova E.E., Sagaydak O.V., Chernevskiy D.K., Belenikin M.S., Krinitsina A.A., Vorontsova M.V., Bodunova N.A., Danishevich A.M., Khatkov I.E., Degterev D.A., Yanova T.I. Breast cancer as part of Cowden syndrome. Malignant tumours. 2022;12(2):36-44. (In Russ.) https://doi.org/10.18027/2224-5057-2022-12-2-36-44