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Article type: Case Report
Authors: Valente, Maria Stella Vasconcelos Salesa; | Mota, Fábio Augusto Xereza | Ricciardi, Bárbara Bezerraa | de Carvalho Borges, Bárbara Matosa | de Lucena Feitosa, Enzo Studarta | de Aquino, Pedro Lucenaa | Valente, Paulla Vasconcelosa; b
Affiliations: [a] Department of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil | [b] Department of Oncology, Oncoclinc, Fortaleza, Ceará, Brazil
Correspondence: [*] Corresponding author: Maria Stella Vasconcelos Sales Valente, University of Fortaleza, Department of Medicine, Washington Soares, 1321 - 60811-905 - Edson Queiroz, Fortaleza, Ceará, Brazil. Tel.: +55 85 34773000; E-mail: [email protected]. ORCID: http://orcid.org/0009-0008-6385-7550
Abstract: INTRODUCTION:Desmoid fibroma (DF) is a disorder characterized by strong clonal proliferation of myofibroblasts and fibroblasts. We describe a case of DF that mimicked a breast tumor, along with a review of the literature on the clinical manifestation, diagnostic process, and course of therapy for this combative disease. CASE REPORT:A 34-year-old female patient with breast lump at the junction of the upper quadrants of the left breast. After the diagnosis of DF, it was decided to perform a sectorectomy of the left breast associated with post-quadrant reconstruction, with immunohistochemistry and findings compatible with DF. DISCUSSION:Clinically manifests as a solid mass that is often painless and occasionally adherent to the chest wall. A treatment strategy should be idealized for each patient. Thus, there is the possibility of performing radical surgery for resection and/or radiotherapy, and surgery may be followed by radiotherapy.
Keywords: Breast, desmoid fibroma, neoplasms
DOI: 10.3233/BD-230028
Journal: Breast Disease, vol. 42, no. 1, pp. 319-323, 2023
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