低温球蛋白血症的肾脏疾病。

Thomas Menter, Helmut Hopfer
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引用次数: 5

摘要

背景:低温球蛋白血症的肾脏疾病很难掌握和诊断,因为它很罕见,血清学检测具有挑战性,容易出现伪影,并且其形态与其他肾脏疾病相同,导致了一系列的鉴别诊断。有时,甚至在免疫荧光和电子显微镜检查后也不能作出明确的诊断。摘要:基于我们在常规诊断和转诊实践中看到的肾活检,我们讨论并说明了与冷球蛋白相关的肾损伤的各种形态学模式。我们概述了与低温球蛋白血症引起的肾脏疾病相关的关键病理生理和临床方面,并描述了电子显微镜下的形态学变化。我们提出了实用的,基于形态学的诊断决策方法,特别考虑了鉴别诊断和疾病模拟。由于在肾活检之前很少检测冷球蛋白,病理学家和临床医生在解释肾活检和管理患者时必须高度怀疑。关键信息:冷球蛋白血症相关性肾小球肾炎(GN)是一种多因素疾病,在临床实践中认识到这一点很重要。提示冷球蛋白相关GN的形态学特征包括膜增殖性GN,有大量单核细胞和(假)血栓的存在。电子显微镜下,主要的诊断特征是单核细胞/巨噬细胞的浸润,系膜和内皮下沉积物的存在,常伴有弯曲的微管/圆柱形和环状亚结构。
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Renal Disease in Cryoglobulinemia.

Background: Renal disease in cryoglobulinemia is difficult to grasp and diagnose because it is rare, serological testing is challenging and prone to artifacts, and its morphology is shared by other renal diseases resulting in a spectrum of differential diagnoses. On occasion, a definitive diagnosis cannot even be rendered after immunofluorescence and electron microscopic studies.

Summary: Based on kidney biopsies seen in our routine diagnostic and referral practice, we discuss and illustrate various morphological patterns of renal injury associated with cryoglobulins. We outline key pathophysiologic and clinical aspects associated with cryoglobulinemia induced renal disease and describe morphologic changes with a focus on electron microscopy. We present our practical, morphology-based approach to diagnostic decision-making with special consideration of differential diagnoses and disease mimickers. Since cryoglobulins are rarely tested for prior to kidney biopsy, pathologists and clinicians alike must have a high level of suspicion when interpreting renal biopsies and managing patients.

Key messages: Cryoglobulinemia-associated glomerulonephritis (GN) is a multifactorial disease which is important to recognize for clinical practice. Morphological features suggestive of cryoglobulinemia-associated GN include a pattern of membranoproliferative GN with abundance of monocytes and the presence of (pseudo)thrombi. By electron microscopy, the main diagnostic features are a prominent infiltration of monocytes/macrophages and the presence of mesangial and subendothelial deposits with frequently curved microtubular/cylindrical and annular substructures.

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