| Literature DB >> 33870121 |
Wei Lin Ng1, Sze Yong Teoh1, Mee Hoong See2, Kartini Rahmat1, Pailoor Jayalakshmi3, Marlina Tanty Ramli4, Mei Sze Teh2, Anushya Vijayananthan1.
Abstract
Desmoid type fibromatosis of the breast is a rare stromal tumor that accounts for <0.2% of all breast tumors. Bilateral and multicentric lesions are extremely rare, with only less than ten cases reported in the literature. Although benign, it is locally aggressive with frequent recurrence in up to almost one-third of the cases. We experienced our first case of bilateral multicentric breast fibromatosis in a 19-year-old woman, with a paternal aunt diagnosed with breast cancer at age 30, who presented to our institution with the chief complaint of retracted nipples for 1 year. The patient denied any history of trauma to her chest. Sonography showed suspicious bilateral hypoechoic masses. Magnetic resonance imaging (MRI) was performed for further evaluation because of the extensive involvement of both the breasts. This report aimed to illustrate the main clinical, radiological, and histopathological characteristics of this rare disease to increase awareness of this entity and discuss the role of MRI. ©Copyright 2021 by Turkish Federation of Breast Diseases Associations.Entities:
Keywords: Desmoid type fibromatosis; breast tumor; fibromatosis; magnetic resonance imaging; ultrasound
Year: 2021 PMID: 33870121 PMCID: PMC8025715 DOI: 10.4274/ejbh.galenos.2020.5482
Source DB: PubMed Journal: Eur J Breast Health