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Leiomyosarcoma of the male breast: Case report

INTRODUCTION: Primary sarcoma in man is very rare and knowledge about this tumor is limited with very few cases published in the literature. CASE REPORT: A 65-year-old man operated on 20 years ago for a left breast tumor with a skin graft at the tumor site (no documentation or pathology report). He...

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Detalles Bibliográficos
Autores principales: Ely Cheikh, Telmoudi, Hamza, Kiram, Hicham, Benaguida, Fatiha, El Miski, Hajar, El Omri, Mustapha, Benhessou, Mohamed, Ennachit, Mohamed, Elkarroumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209182/
https://www.ncbi.nlm.nih.gov/pubmed/34168877
http://dx.doi.org/10.1016/j.amsu.2021.102495
Descripción
Sumario:INTRODUCTION: Primary sarcoma in man is very rare and knowledge about this tumor is limited with very few cases published in the literature. CASE REPORT: A 65-year-old man operated on 20 years ago for a left breast tumor with a skin graft at the tumor site (no documentation or pathology report). He consulted for a mass in the left breast, bleeding on contact, associated with nodules in the right breast that looked suspicious. On breast ultrasound, a tissue formation in the lower medial quadrant of the left breast with irregular contours, measuring 42 × 53mm with the presence of several suspicious tissue formations in the right breast, the largest measuring 2 × 2cm. Surgical removal of the left mass with a right mastectomy with pathology report of breast leiomyosarcoma with healthy surgical borders followed by radiotherapy for local control. DISCUSSION: Leiomyosarcoma is an extremely rare tumor in the breast and usually originates from the blood vessels, myoepithelium, or nipple musculature, as in our case. Breast sarcomas represent less than 1% of all malignant neoplasms of the breast. Their incidence in women is much higher than in men. CONCLUSION: Primary breast sarcomas are rare tumors that originate from the mesenchymal tissue of the breast and represent less than 1% of all malignant neoplasms of the breast. Their diagnosis is confirmed by biopsy with immunohistochemical and only surgery can guarantee cure. Radiotherapy is recommended for local control after surgery.