Klank David, Hoffmann Martin, Porubsky Stefan, Bergner Raoul
Medizinische Klinik A, Klinikum der Stadt Ludwigshafen gGmbH, Bremserstrasse 79, 67063 Ludwigshafen, Germany.
Institut für Pathologie, Universitätsklinikum Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
Diagnostics (Basel). 2022 Aug 7;12(8):1912. doi: 10.3390/diagnostics12081912.
: The simultaneous occurrence of impaired kidney function and paraproteinemia is common in our constantly aging society. Both can be independent entities; however, renal insufficiency can also be caused by the paraprotein. We assessed all kidney biopsies in patients with monoclonal gammopathy in our clinic over the past 20 years and evaluated the histological results. : Biopsies were systematically performed in nearly all patients with paraproteinemia and impaired kidney function ( = 178). The histological findings were systematically evaluated and correlated with the initial clinical diagnosis. : We found cast nephropathy (CN) in = 66 (37.1%) biopsies, AL amyloidosis in = 31 (17.4%) biopsies, monoclonal immunoglobulin deposition disease (MIDD) in = 7 (3.9%) biopsies and other renal diseases (ORDs) in = 74 (41.6%) biopsies. In the latter group, paraprotein-associated changes were found in 37 of 74 (50%) patients, whereas paraprotein-independent changes were found in the other half. Whereas, in the group of patients with MGUS, the findings were heterogenous, most of the patients with known multiple myeloma (MM) or B-NHL showed malignancy-associated changes in the kidney. The biopsy changed the diagnoses in a significant proportion of the patients: The group of patients with MM grew from 71 to 112 patients, whereas, in the MGUS group, only 31 of 44 patients remained. : Kidney biopsies in patients with paraproteinemia and renal impairment show a wide range of findings that can lead to a change in diagnosis.
在我们这个不断老龄化的社会中,肾功能受损和副蛋白血症同时出现的情况很常见。两者都可能是独立的病症;然而,肾功能不全也可能由副蛋白引起。我们评估了过去20年里在我们诊所进行单克隆丙种球蛋白病患者的所有肾脏活检,并对组织学结果进行了评估。:几乎所有患有副蛋白血症和肾功能受损的患者(n = 178)都进行了系统的活检。对组织学结果进行了系统评估,并与初始临床诊断相关联。:我们在n = 66(37.1%)例活检中发现管型肾病(CN),在n = 31(17.4%)例活检中发现AL淀粉样变性,在n = 7(3.9%)例活检中发现单克隆免疫球蛋白沉积病(MIDD),在n = 74(41.6%)例活检中发现其他肾脏疾病(ORDs)。在后者组中,74例患者中有37例(50%)发现了与副蛋白相关的变化,而另一半患者发现了与副蛋白无关的变化。然而,在意义未明的单克隆丙种球蛋白病(MGUS)患者组中,结果是异质性的,大多数已知多发性骨髓瘤(MM)或B细胞非霍奇金淋巴瘤(B-NHL)的患者在肾脏中显示出与恶性肿瘤相关的变化。活检在相当一部分患者中改变了诊断:MM患者组从71例增加到112例,而在MGUS组中,44例患者中只有31例保持原来诊断。:患有副蛋白血症和肾功能损害的患者的肾脏活检显示出广泛的结果,这些结果可能导致诊断的改变。