乳腺弥漫性大b细胞淋巴瘤:一个病例系列。

IF 3 Q2 Medicine
Clinical Medicine Insights-Blood Disorders Pub Date : 2017-08-14 eCollection Date: 2017-01-01 DOI:10.1177/1179545X17725034
Afaf H Al Battah, Einas A Al Kuwari, Zsolt Hascsi, Abdulqadir J Nashwan, Halima Elomari, Hisham Elsabah, Safa Al Azawi, Samah Kohla, Dina Soliman, Mohamed A Yassin
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引用次数: 4

摘要

原发性乳腺淋巴瘤(PBL)是一种罕见的疾病,在以往的研究中很少讨论该病的临床组织病理学特征。它占结外淋巴瘤的2.2%,占乳腺恶性肿瘤的0.04%至0.5%,尽管乳腺淋巴瘤和癌在临床和影像学上有相似之处,但文献报道的预后却各不相同。对于治疗PBL的最佳方法尚无共识。然而,放疗和化疗被单独或联合用于治疗各种PBL病例。我们回顾性研究了2012年至2015年间在卡塔尔某三级癌症中心就诊的3例乳腺PBL患者,试图确定PBL的共同临床特征、治疗方法和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Diffuse Large B-Cell Breast Lymphoma: A Case Series.

Diffuse Large B-Cell Breast Lymphoma: A Case Series.

Diffuse Large B-Cell Breast Lymphoma: A Case Series.

Diffuse Large B-Cell Breast Lymphoma: A Case Series.

Primary breast lymphoma (PBL) is a rare disease, and few clinicohistopathologic features of the disease have been discussed in previous studies. It represents 2.2% of extranodal lymphomas and constitutes 0.04% to 0.5% of malignant breast neoplasms, despite the clinical and radiographic similarities between breast lymphoma and carcinoma, the prognosis, as reported in the literature, varies. No consensus exists on the best way to treat PBL. However, radiotherapy and chemotherapy were used alone or in combination to treat various cases of PBL. We retrospectively studied 3 cases of PBL of the breast seen in patients attending a tertiary cancer center in Qatar, between 2012 and 2015, in an attempt to determine the common clinical features, therapy, and prognosis of PBL.

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来源期刊
CiteScore
3.70
自引率
0.00%
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审稿时长
8 weeks
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