肾脏原发性MALT淋巴瘤。

M Colović, J Hadzi-Djokić, V Cemerikić, R Colović, G Janković, M Dacić
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引用次数: 26

摘要

本文报道一例50岁男性原发性粘膜相关淋巴组织肿瘤(MALT),他患有顽固性高血压超过15年。常规检查时发现右肾肿块(6x5x3 cm),经CT扫描和核磁共振证实。患者接受肾切除术。发现一肿块累及肾脏、肾盂及输尿管上部。组织学表现为MALT型低级别非霍奇金b细胞淋巴瘤。肿瘤细胞单克隆抗体CD20、cd79 α、表面和细胞质及IgM免疫球蛋白阳性,呈轻链限制性反应(kappa+)。在获得组织学资料后,进行仔细的分期。这种疾病在其他地方没有发现。结论:该患者属于原发性肾MALT淋巴瘤IE期。胃镜检查显示慢性浅表性胃炎。尿素酶试验阳性,检出抗幽门螺杆菌IgG抗体,滴度421。除幽门螺杆菌外,未给予其他治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary MALT lymphoma of the kidney.

A primary mucosa associated lymphoid tissue tumor (MALT) of the kidney in a 50-year-old man who suffered from on therapy resistant high blood pressure over 15 years period is presented. A mass in the right kidney (6x5x3 cm) during routine check up was discovered on ultrasonography and confirmed on CT scan and NMR. The patient was submitted to nephrectomy. A mass involving kidney, pyelon and upper part of the ureter was found. Histology showed low grade non-Hodgkin B-cell lymphoma of MALT type. The neoplastic cells were positive for monoclonal antibodies CD20, CD79alpha, surface and cytoplasmic and IgM immunoglobulins and showed light chain restriction (kappa+). After histology was available, a careful staging was performed. The disease was not found anywhere else. It was concluded that the patient belonged to the stage IE of primary kidney MALT lymphoma. Gastroscopy showed signs of chronic superficial gastritis. Urease test was positive and IgG antibodies against Helicobacter pylori in titer 421 were found as well. Except for Helicobacter pylori no additional therapy was given.

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