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膜增生性肾小球肾炎与结直肠癌的相关性-一例报告。

Association Between Membranoproliferative Glomerulonephritis and Colorectal Cancer - A Case Report.

机构信息

1University Clinic of Nephrology, Faculty of Medicine, "Ss. Cyril and Methodius", University in Skopje, RN Macedonia.

2Department of Abdominal Surgery, University Surgery Hospital "St. Naum Ohridski", 1000 Skopje, RN Macedonia.

出版信息

Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2024 Jul 15;45(2):31-36. doi: 10.2478/prilozi-2024-0013. Print 2024 Jun 1.

Abstract

Membranoproliferative glomerulonephritis (MPGN) is a rare glomerular disease characterized by mesangial hypercellularity and thickening of the glomerular basement membrane (GBM). MPGN can be idiopathic or associated with malignancy, systemic immune complex disorders and chronic infections. It has rarely been associated with solid organ tumors, such as lung, gastric, breast or prostate cancer. We report a patient with MPGN and coexisting colorectal carcinoma. A 48-year-old man presented with anemia, loss of weight, hypertension, and nephrotic syndrome. The renal biopsy findings were compatible with type 1 MPGN. The antineutrophilic cytoplasmic antibodies, antinuclear antibodies, anti-GBM, serologic markers of hepatitis B and hepatitis C and tumor markers were negative. After ruling out the secondary causes of MPGN, the patient was treated with pulse doses of methylprednisolone and a single dose of cyclophosphamide. However, due to the worsening anemia and rectal bleeding, a colonoscopy was performed, which established a diagnosis of adenocarcinoma of the descending colon. The patient was treated with left hemicolectomy and oral corticosteroids. Within a year after the cancer treatment, the patient experienced a complete resolution of the proteinuria and improvement of the kidney function. Although rare, MPGN can be associated with hematologic malignancies and solid organ tumors. The most common causes of secondary MPGN should be ruled out before starting specific treatment. In our patient, cancer treatment has led to a subsequent remission of the nephrotic syndrome, which indicated that this association was not coincidental but rather causal. In patients with a tumor and concomitant glomerulopathy which is suspected to be paraneoplastic in etiology, the treatment of the underlying malignancy should be prioritized.

摘要

膜增生性肾小球肾炎(MPGN)是一种罕见的肾小球疾病,其特征为系膜细胞增生和肾小球基底膜(GBM)增厚。MPGN 可为特发性或与恶性肿瘤、系统性免疫复合物疾病和慢性感染相关。它很少与实体器官肿瘤相关,如肺癌、胃癌、乳腺癌或前列腺癌。我们报告一例 MPGN 合并结直肠癌患者。一名 48 岁男性因贫血、体重减轻、高血压和肾病综合征就诊。肾活检结果符合 1 型 MPGN。抗中性粒细胞胞质抗体、抗核抗体、抗 GBM、乙型肝炎和丙型肝炎血清标志物及肿瘤标志物均为阴性。在排除 MPGN 的继发性病因后,患者接受了甲基强的松龙脉冲治疗和环磷酰胺单剂量治疗。然而,由于贫血恶化和直肠出血,进行了结肠镜检查,确立了降结肠癌腺癌的诊断。患者接受了左半结肠切除术和口服皮质类固醇治疗。在癌症治疗后 1 年内,患者蛋白尿完全缓解,肾功能改善。尽管罕见,但 MPGN 可与血液系统恶性肿瘤和实体器官肿瘤相关。在开始特定治疗之前,应排除继发性 MPGN 的常见病因。在我们的患者中,癌症治疗导致随后肾病综合征缓解,这表明这种关联并非巧合,而是因果关系。对于肿瘤合并疑似副肿瘤病因的肾小球病患者,应优先治疗基础恶性肿瘤。

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