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首页> 外文期刊>Archives of Gynecology and Obstetrics >Primary diffuse large B cell lymphoma of the breast eight years after the diagnosis of gastric MALT lymphoma: report of first case
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Primary diffuse large B cell lymphoma of the breast eight years after the diagnosis of gastric MALT lymphoma: report of first case

机译:胃MALT淋巴瘤确诊八年后乳腺原发性弥漫性大B细胞淋巴瘤:第一例报道

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摘要

Primary breast lymphoma (PBL) is an uncommon type of extranodal non-Hodgkin’s lymphoma (NHL), accounting for approximately 1% of all extranodal NHL. Diffuse large B cell lymphoma (DLBCL) is the most frequent histology. Both primary mucosa-associated lymphoid tissue (MALT) lymphoma of the breast and its relapse have been documented previously. We report on a 63-year-old woman with primary DLBCL of the breast which was diagnosed 8 years after gastric MALT lymphoma. Following chemotherapy, complete response was obtained. We suggest that for women presenting with a breast mass who received cytotoxic treatment for the other lymphoma, PBL should be considered in the differential diagnosis of the breast mass together with primary breast carcinoma.
机译:原发性乳腺淋巴瘤(PBL)是结外型非霍奇金淋巴瘤(NHL)的罕见类型,约占所有结外NHL的1%。弥漫性大B细胞淋巴瘤(DLBCL)是最常见的组织学。乳腺的原发性粘膜相关淋巴样组织(MALT)淋巴瘤及其复发都已被记录。我们报道了一名63岁的女性,原发性乳腺DLBCL,在胃MALT淋巴瘤发生8年后被诊断出。化疗后,获得了完全的反应。我们建议,对于患有乳腺肿块且接受其他淋巴瘤细胞毒性治疗的妇女,在乳腺肿块与原发性乳腺癌的鉴别诊断中应考虑使用PBL。

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