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Successful treatment of biphasic metaplastic sarcomatoid carcinoma of the breast by evaluation of immunohistochemical markers
Hematology, Oncology and Stem Cell Therapy. 2010; 3 (2): 89-93
Dans Anglais | IMEMR | ID: emr-98067
ABSTRACT
Biphasic metaplastic sarcomatoid carcinoma [MSC] of the breast is rare and aggressive. Patients with metaplastic breast carcinomas tend to have poor outcomes with a high risk of recurrence following primary surgery. Most reports have shown that systemic therapy appears to be less effective. We report a case of a 42-year-old female who presented with a large [14 cm] cauliflower breast mass. Biopsy revealed a poorly differentiated sarcoma. Initially, neo-adjuvant concurrent chemoradiotherapy with a sarcoma regimen was prescribed, and the tumor regressed to a large ulcer. Subsequent biopsy showed invasive ductal carcinoma [estrogen receptor, progesterone receptor stained weakly, 5%, Her22+] and disappearance of the sarcomatous component. Second-line neoadjuvant therapy was designed according to the histologic features of infiltrating ductal carcinoma, which led to nearly a complete response. A modified radical mastectomy of the right breast and axillary dissection was performed followed by monoclonal antibody [trastuzumab] therapy for 6 months due to the surgical specimen showing Her23+. The treatment course went smoothly with a good response. The patient had no evidence of disease at 18 months
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Indice: Méditerranée orientale Sujet Principal: Tumeurs du sein / Immunohistochimie / Marqueurs biologiques tumoraux / Résultat thérapeutique Type d'étude: Enquête cas-témoins / Études cas/témoins Limites du sujet: Adulte / Femelle / Humains langue: Anglais Texte intégral: Hematol. Oncol. Stem Cell Ther. Année: 2010

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Recherche sur Google
Indice: Méditerranée orientale Sujet Principal: Tumeurs du sein / Immunohistochimie / Marqueurs biologiques tumoraux / Résultat thérapeutique Type d'étude: Enquête cas-témoins / Études cas/témoins Limites du sujet: Adulte / Femelle / Humains langue: Anglais Texte intégral: Hematol. Oncol. Stem Cell Ther. Année: 2010