乳腺弥漫性大细胞B型淋巴瘤1例

Lamyae Nouiakh, K. Oualla, Imane Ouafki, S. Berrad, H. Erraichi, Y. Dkhissi, L. Amaadour, Z. Benbrahim, S. Arifi, M. Boubou, H. Fatemi, N. Mellas
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摘要

背景:原发性乳腺淋巴瘤是一种非常罕见的疾病。弥漫性大B细胞亚型是最常见的组织学类型。临床表现无特异性;它可能与乳腺癌中发现的相似。诊断仅保留在明确的组织学分析后。这些淋巴瘤的处理与其他局部没有什么不同。我们报告一例原发性乳腺弥漫性大B细胞淋巴瘤收集在非斯哈桑二医院的内科肿瘤科在一个32岁的病人。通过这项工作,我们将讨论这些肿瘤的流行病学、临床、临床旁、组织学、治疗和预后特征。病例介绍:一名32岁女性因左乳结节发展3个月就诊。临床检查发现左侧乳房无痛性肿块,无炎性征象,同侧腋窝腺病3cm。乳房x光检查和乳腺超声检查发现3个组织病变,最大的为左乳,大小为26mm,并伴有同侧腋窝腺病。进行显微活检。组织学分析显示,乳腺薄壁组织基本游离,呈弥漫性大细胞结构。免疫组化结果显示,肿瘤细胞抗cd20抗体阳性。胸腹计算机断层扫描的扩展评估未显示乳房x光检查和超声检查发现的乳腺病变外的任何继发性定位。决定用R-CHOP化疗,但患者出于家庭原因拒绝接受治疗。结论:通过本工作,我们报告了一例DLBCL,并对文献进行了回顾。总之,DLBCL是乳腺淋巴瘤最常见的组织学亚型。常规化疗后的巩固放疗仍然是治疗DLBCL患者最合理的治疗方式。有必要进行大规模的研究,以确定影响生存的因素,以改善这些淋巴瘤患者的管理。
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 cell type B breast lymphoma: case report
Background: Primary breast lymphoma is a very rare disease. The diffuse large B cell subtype is the most common histological variety. The clinical presentation is non-specific; it can be similar to that found in breast carcinoma. The diagnosis is only retained after a definitive histological analysis. The management of these lymphomas is no different from that of other localizations. We report the case of primary breast diffuse large B cells lymphoma collected at the medical oncology department of the Hassan II Hospital of Fez in a 32-year-old patient. Through this work, we will discuss the epidemiological, clinical, paraclinical, histological, therapeutic, and prognostic characteristics of these tumors. Case presentation: A 32-year-old woman consulted for a left breast nodule evolving for 3 months. Clinical examination objectified a painless mass of the left breast without inflammatory signs and homolateral axillary adenopathy of 3cm. Mammography and breast ultrasound were performed objectifying three tissue lesions measuring 26mm for the largest in the left breast, associated with homolateral axillary adenopathy. A micro biopsy was performed. Histological analysis showed breast parenchyma largely dissociated by cell proliferation of diffuse architecture with large cells. In immunohistochemistry, tumor cells were positive for the anti-CD20 antibody. An extension assessment with thoracoabdominalcomputed tomographydid not show any secondary localization outside the breast lesions found in the mammography and ultrasound. Chemotherapy with R-CHOP was decided, but the patient refused to be treated for family reasons. Conclusion: Through this work, a case of DLBCL was reported with a review of the literature. In summary, the DLBCL histological subtype is the most frequent form of mammary lymphoma. Consolidation radiotherapy after conventional chemotherapy remains the most reasonable therapeutic modality for the treatment of patients with DLBCL. Large studies are necessary to identify the factors that influence survival, to improve the management of patients with these lymphomas.
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