학술논문

Early onset, multiple, bilateral fibroadenomas of the breast: a case report
Document Type
article
Source
BMC Women's Health. 21(1)
Subject
Health Services and Systems
Biomedical and Clinical Sciences
Health Sciences
Oncology and Carcinogenesis
Clinical Research
Prevention
Breast Cancer
Genetics
Cancer
Detection
screening and diagnosis
Aetiology
2.1 Biological and endogenous factors
4.1 Discovery and preclinical testing of markers and technologies
Adolescent
Breast
Breast Diseases
Breast Neoplasms
Female
Fibroadenoma
Genetic Testing
Humans
PTEN
Genetic testing
Case report
Nursing
Paediatrics and Reproductive Medicine
Public Health and Health Services
Obstetrics & Reproductive Medicine
Reproductive medicine
Midwifery
Public health
Language
Abstract
BackgroundWhile fibroadenomas are common in the general population, affecting 10-20% of women, they are rarely early-onset, multiple, and bilateral.Case presentationAn 18-year-old woman presented with a 6 year history of multiple, bilateral breast masses without family history of breast disease. Magnetic resonance imaging (MRI, Fig. 1) of the breasts showed innumerable, bilateral breast masses ranging in size from 0.5 to 4 cm. Two needle biopsies showed fibroadenoma. Although the patient's family history did not meet National Comprehensive Cancer Network (NCCN) guidelines for genetic testing, it was performed due to the rarity of her presentation. Genetic testing identified a pathogenic mutation in the phosphatase and tensin homolog (PTEN) gene.ConclusionsA germline mutation in PTEN is associated with an increased risk of breast cancer and often occurs as part of Cowden Syndrome. This case highlights the importance of genetic testing in patients with unusual presentations of early-onset, bilateral, and multiple (greater than four) fibroadenomas.