Primary malignant lymphoma of the kidney: case report and literature review.

General & diagnostic pathology Pub Date : 1998-04-01
M J Fernandez-Aceñero, M Galindo, O Bengoechea, P Borrega, J J Reina, R Carapeto
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Abstract

We report on a 65-year-old white woman who was hospitalized because of symptoms of an acute adrenocortical insufficiency. A CT scan revealed the presence of a large mass in the left kidney that infiltrated the adrenal gland. Fine needle aspiration cytology of the mass under imaging control failed to achieve a correct diagnosis, and nephrectomy was undertaken with a preoperative diagnosis of renal cell carcinoma. However, the frozen section reveals a neoplasm of large lymphoid cells with a diffuse growth pattern. Immunohistochemistry confirms the B-cell nature of the neoplasm (CD20+). The final diagnosis was non-Hodgkin B-cell high grade centroblastic lymphoma (KIEL classification). Postoperative studies failed to show lymph node or bone marrow infiltration by neoplastic cells. We found reports on only 60 malignant lymphomas, considered to be primary to the kidney. They usually affect middle-aged people, can be diagnosed with imaging techniques, and seem to show a better prognosis than other types of lymphoma.

原发性肾恶性淋巴瘤:病例报告及文献复习。
我们报告一位65岁的白人妇女因急性肾上腺皮质功能不全而住院。CT扫描显示左肾有一个大肿块浸润到肾上腺。肿块在影像学控制下的细针穿刺细胞学未能得到正确诊断,术前诊断为肾细胞癌,行肾切除术。然而,冰冻切片显示一个弥漫生长模式的大淋巴样细胞肿瘤。免疫组织化学证实肿瘤的b细胞性质(CD20+)。最终诊断为非霍奇金b细胞高级别中心母细胞淋巴瘤(KIEL分类)。术后研究未发现肿瘤细胞浸润淋巴结或骨髓。我们发现只有60例恶性淋巴瘤的报告,被认为是原发于肾脏。它们通常影响中年人,可以通过影像学技术诊断,似乎比其他类型的淋巴瘤预后更好。
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