Desmoid tumor in the male breast refractory to systemic treatment: case report

Desmoid-type fibromatosis, an intermediate soft tissue tumor known for its local infiltrative behavior and high recurrence rate, is uncommon in the male breast. The report outlines the clinical journey of a 44-year-old male presenting with a rapidly growing breast mass, initially managed with a watchful waiting approach and subsequent systemic therapies including celecoxib, sorafenib, and a combination of methotrexate and vinblastine, all of which proved ineffective. Genetic testing revealed a catenin beta 1 (CTNNB1) mutation, indicative of a sporadic tumor. Despite various treatment attempts, significant tumor progression was observed, necessitating surgical intervention followed by radiotherapy. This case underscores the challenges in managing desmoid tumors, emphasizing the importance of multidisciplinary approaches and the potential need for surgical resection when conventional therapies fail.

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Publication Details

Journal
Mastology
Published
2025-02-27
DOI
https://doi.org/10.29289/2594539420240024
Primary Topic
Soft tissue tumor case studies
Type
article
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0.00
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article

Desmoid tumor in the male breast refractory to systemic treatment: case report

Juliana Alves de Souza, Almir Galvão Vieira Bitencourt, Cândida Maria Alves Soares, Camila Souza Guatelli et al.
Mastology
Soft tissue tumor case studies
article

Desmoid tumor in the male breast refractory to systemic treatment: case report

Juliana Alves de Souza, Almir Galvão Vieira Bitencourt, Cândida Maria Alves Soares, Camila Souza Guatelli, Luciana Graziano, Bianca Miranda Lago, Soraia Quaranta Damião, Clifton Rodrigues
article en

Abstract

Desmoid-type fibromatosis, an intermediate soft tissue tumor known for its local infiltrative behavior and high recurrence rate, is uncommon in the male breast. The report outlines the clinical journey of a 44-year-old male presenting with a rapidly growing breast mass, initially managed with a watchful waiting approach and subsequent systemic therapies including celecoxib, sorafenib, and a combination of methotrexate and vinblastine, all of which proved ineffective. Genetic testing revealed a catenin beta 1 (CTNNB1) mutation, indicative of a sporadic tumor. Despite various treatment attempts, significant tumor progression was observed, necessitating surgical intervention followed by radiotherapy. This case underscores the challenges in managing desmoid tumors, emphasizing the importance of multidisciplinary approaches and the potential need for surgical resection when conventional therapies fail.

MastologyVol. 34
AC Camargo Hospital (BR)
Openalex Percentile: Top 94%
Soft tissue tumor case studies
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