Concomitant Nephrotic Syndrome and Cryoglobulinemia in a Case of Malignant Mesothelioma.

Case Reports in Nephrology Pub Date : 2022-09-28 eCollection Date: 2022-01-01 DOI:10.1155/2022/8677293
Kei Nagai, Hiroaki Tachi, Kohei Inoue, Atsushi Ueda
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引用次数: 1

Abstract

Malignant pleural mesothelioma is rarely associated with nephrotic syndrome. Cryoglobulinemia is found in various pathological statuses, such as hepatitis C virus infection but rarely in malignant neoplasms. We recently encountered a patient with malignant mesothelioma coincident with nephrotic syndrome and cryoglobulinemia in the course of chemotherapy. A 60-year-old man employed as a building painter was diagnosed with malignant mesothelioma by lung biopsy two years earlier and was started on chemotherapy. Nivolumab seemed effective in controlling mesothelioma, but skin immune-related adverse events occurred during the course of treatment. After discontinuation of nivolumab and administration of gemcitabine as an alternative therapy, the patient was referred to a nephrologist because of the subsequent development of edema, renal injury, and proteinuria. Following the investigation, he was diagnosed with nephrotic syndrome and cryoglobulinemia with C4-dominant cold activation. However, a percutaneous renal biopsy could not be performed due to persistent severe cough induced by pleural involvement. The patient died a little over three years after the pathological diagnosis of pleural mesothelioma. Our case had three key features nephrotic syndrome was possibly associated with malignant mesothelioma; cryoglobulinemia occurred in malignant mesothelioma; and concomitant nephrotic syndrome and cryoglobulinemia occurred after chemotherapy. Unfortunately, our rare case lacks a basis in renal pathology or evidence of links between the pathogenesis of malignant mesothelioma, cryoglobulinemia, and nephrotic syndrome. This case does not provide a causal mechanism, but may be worth adding to the case list as one of the rare renal involvement in a patient with malignant mesothelioma.

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恶性间皮瘤并发肾病综合征和冷球蛋白血症1例。
恶性胸膜间皮瘤很少与肾病综合征相关。冷球蛋白血症见于各种病理状态,如丙型肝炎病毒感染,但很少见于恶性肿瘤。我们最近遇到一个恶性间皮瘤患者在化疗过程中同时伴有肾病综合征和冷球蛋白血症。一名60岁的建筑油漆工两年前通过肺活检诊断为恶性间皮瘤,并开始化疗。尼武单抗在控制间皮瘤方面似乎有效,但在治疗过程中发生了与皮肤免疫相关的不良事件。在停用纳武单抗并给予吉西他滨作为替代治疗后,由于随后出现水肿、肾损伤和蛋白尿,患者被转介到肾病科。经过调查,他被诊断为肾病综合征和低温球蛋白血症,伴有c4显性冷活化。然而,由于胸膜受累引起的持续严重咳嗽,无法进行经皮肾活检。病人在病理诊断为胸膜间皮瘤后三年多一点死亡。本病例有三个主要特征:肾病综合征可能与恶性间皮瘤有关;恶性间皮瘤发生冷球蛋白血症;化疗后并发肾病综合征和冷球蛋白血症。不幸的是,我们罕见的病例缺乏肾脏病理学基础或恶性间皮瘤、冷球蛋白血症和肾病综合征发病机制之间联系的证据。该病例没有提供病因机制,但作为恶性间皮瘤患者罕见的肾脏累及病例之一,可能值得添加到病例列表中。
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来源期刊
Case Reports in Nephrology
Case Reports in Nephrology Medicine-Nephrology
CiteScore
1.70
自引率
0.00%
发文量
32
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