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dc.contributor.authorTrinh Le Huy, Tran Dinh Anh-
dc.date.accessioned2023-02-08T09:08:05Z-
dc.date.available2023-02-08T09:08:05Z-
dc.date.issued2021-
dc.identifier.urihttp://thuvienso.thanglong.edu.vn//handle/TLU/5642-
dc.descriptionSố 148 E9 (12): Tr. 102-107vi
dc.description.abstractPrimary breast diffuse large B-cell lymphoma (DLBCL) is a rare non-Hodgkin’s lymphoma with limited data. We here report a case of primary breast diffuse large B-cell lymphoma mimicking breast cancer. A 52-year old woman had a painless mass in her right breast. Fine needle aspiration cytology and core biopsy were performed which suggested malignant features but could not confirm the specific subtype. Excisional biopsy then was conducted revealing non-Hodgkin lymphoma, which was subsequently confirmed with histopathology and diagnosed as diffuse large B-cell lymphoma (DLBCL). A chest computed tomography scan revealed a 3.5cm sized breast mass with skin thickening and modest lymphadenopathy in the ipsilateral axilla. The patient received six courses of R-CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone plus rituximab) chemotherapy, then whole breast radiation (30Gy in 15 fractions). At 12 months of follow-up, the patient survives with no evidence of disease. No morbidities occurred in this patient during the follow-up period. We briefly review the current practice pattern in patients with primary breast diffuse large B-cell lymphomavi
dc.language.isoenvi
dc.publisherJournal of Medical Researchvi
dc.subjectPrimary breast lymphoma (PBL)vi
dc.subjectDLBCLvi
dc.titleA case of primary breast diffuse large B cell lymphomavi
dc.typeArticlevi
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