Primary, nodal, marginal zone lymphoma of a woman’s left breast imitated fibroadenoma

S. Strashilov, A. Yordanov, V. Nanev, M. Mihailova
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Abstract

Background Primary breast lymphoma is a rare malignant neoplastic disease, accounting for around 0.5 per cent of all malignant diseases of that organ, and also 2.2 per cent of extranodal lymphomas. The most common histopathological types are: diffuse large B-cell lymphoma, extranodal B-cell marginal zone lymphoma and MALT lymphoma. The primary affected group is with median age between 55 and 62 years. The clinical manifestation is usually of a tumour process in the affected breast. Case presentation Here we present an extremely rare case of a 68 years old woman with primary, nodal, B-cell, marginal zone lymphoma of the left breast, presenting itself under the mask of a benign tumour process, found accidentally following a histopathological examination of excisional samples. Conclusions Primary, nodal, marginal zone, B-cell lymphoma of the breast is extremely rare. Its clinical and mammographic presentation completely overlaps with those of fibroadenoma, which makes diagnosing it preoperatively practically impossible. Main treatment method here is not surgical, but radiological and chemotherapeutic.
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女性左乳原发性淋巴结边缘区淋巴瘤,模仿纤维腺瘤
原发性乳腺淋巴瘤是一种罕见的恶性肿瘤疾病,约占该器官所有恶性疾病的0.5%,也占结外淋巴瘤的2.2%。最常见的组织病理类型有:弥漫性大b细胞淋巴瘤、结外b细胞边缘区淋巴瘤和MALT淋巴瘤。主要受影响人群的中位年龄在55岁至62岁之间。临床表现通常是在受影响的乳房肿瘤进程。我们报告一例极为罕见的68岁女性左乳房原发性淋巴结b细胞边缘区淋巴瘤,在良性肿瘤的掩盖下表现出来,在切除样本的组织病理学检查中意外发现。结论乳腺原发性、淋巴结性、边缘带性b细胞淋巴瘤极为罕见。它的临床和乳房x线摄影表现与纤维腺瘤完全重叠,这使得术前诊断几乎不可能。主要的治疗方法不是手术,而是放疗和化疗。
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Australasian Medical Journal
Australasian Medical Journal MEDICINE, GENERAL & INTERNAL-
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