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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. Byakhova
City Clinical Oncological Hospital No. 1
Russian Federation

Mariya M. Byakhova, MD, PhD, Head of the Genetics Laboratory, Center for Pathological Anatomical Diagnostics and Molecular Genetics

Moscow 



A.  B. Semenova
City Clinical Oncological Hospital No. 1
Russian Federation

Anna B. Semenova, MD, PhD, DSc, Head of the Center for Pathological Diagnosis and Molecular Genetics

Moscow



V.  N. Galkin
City Clinical Oncological Hospital No. 1
Russian Federation

Vsevolod N. Galkin, MD, PhD, DSc, Professor, Chief of Medicine

Moscow



C.  V. Homushku
City Clinical Oncological Hospital No. 1
Russian Federation

Chinchi V. Homushku, Laboratory Geneticist, Genetics Laboratory, Center for Pathological Diagnosis and Molecular Genetics

Moscow



A.  E. Zod»binova
City Clinical Oncological Hospital No. 1
Russian Federation

Aisa E. Zod»binova, Laboratory Geneticist, Genetics Laboratory, Center for Pathological Diagnosis and Molecular Genetics

Moscow



M.  V. Makarova
Evogen LLC
Russian Federation

Maria V. Makarova, Geneticist, Oncologist, Head of Oncology Genetics

Moscow



E.  E. Baranova
Evogen LLC; Russian Medical Academy of Continuous Professional Education
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
Evogen LLC
Russian Federation

Olesya V. Sagaydak, MD, PhD, Head of the Scientific and Medical Department

Moscow



D.  K. Chernevskiy
Evogen LLC
Russian Federation

Denis K. Chernevsky, Clinical Sequencing Expert

Moscow



M.  S. Belenikin
Evogen LLC
Russian Federation

Maxim S. Belenikin, MD, PhD сhemistry, Head of the Laboratory and Director for Science and Development

Moscow



A.  A. Krinitsina
Evogen LLC
Russian Federation

Anastasia A. Krinitsyna, MD, PhD biol., Deputy Head of the Laboratory

Moscow



M.  V. Vorontsova
National Medical Research Center for Endocrinology
Russian Federation

Maria V. Vorontsova, MD, PhD, Pediatric Endocrinologist, Leading Researcher, Department of Pediatric Thyroidology, Reproductive and Somatic Development

Moscow 



N.  A. Bodunova
Moscow Clinical Research Center named after A. S. Loginov
Russian Federation

Natalya A. Bodunova, MD, PhD, Gastroenterologist, Head of the Center for Personalized Medicine

Moscow



A.  M. Danishevich
Moscow Clinical Research Center named after A. S. Loginov
Russian Federation

Anastasia M. Danishevich, Geneticist, Center for Personalized Medicine

Moscow



I.  E. Khatkov
Moscow Clinical Research Center named after A. S. Loginov
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
Moscow Clinical Research Center named after A. S. Loginov
Russian Federation

Moscow 



T.  I. Yanova
Moscow Clinical Research Center named after A. S. Loginov
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

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