Rechtina I G, Golitsina E P, Varlamova E Iu, Varshvskiĭ V A, Kireeva A A, Biriukova L S, Savchenko V G
Ter Arkh. 2013;85(3):80-5.
To study the pathomorphology of kidneys in patients with multiple myeloma (MM) and severe renal failure (RF) and to compare the results of morphological, immunohistochemical, and electron microscopic examinations of nephrobiopsy specimens with the pattern of monoclonal secretion and the type of proteinuria and paraproteinuria.
A study group comprised 25 patients with MM and severe RF; 22 of them underwent programmed hemodialysis. Immunochemical study of serum and urine proteins, renal puncture biopsy with light, immunofluorescence and electron microscopy examination of its specimens were performed in all the patients.
Cast nephropathy (CN) is the most common type of renal impairment in patients with MM and severe RF. CN concurrent with monoclonal immunoglobulin deposition disease was identified in 32% of cases. In the mixed lesion, it is CN that is a determinant in the development of acute and chronic RF. Rare variants of nephropathies as fibrillary glomerulonephritis, immunotactoid nephropathy, and crystalline histiocytosis were found in 16% of cases. In most cases, severe RF in MM develops in case of low monoclonal secretion. However, there are a larger number of secreted and excreted monoclonal light chains in CN than in other variants of kidney lesion. Urinary paraprotein G excretion suggests that the glomerular filter is damaged. Degenerative changes in the podocytes and a reduction in their small processes were detected in the majority of cases. In glomerular or mixed proteinuria, there were also unorganized and organized deposits in the glomerular basement membrane.
The pattern of nephropathy does not determine a renal response after chemotherapy. The reversibility of CN in MM depends on the magnitude of interstitial fibrosis and podocyte changes. The pronounced changes in the podocytes as a reduction in their small processes serves as a poor sign in achieving renal responses following chemotherapy.
研究多发性骨髓瘤(MM)合并严重肾衰竭(RF)患者的肾脏病理形态学,并将肾活检标本的形态学、免疫组织化学和电子显微镜检查结果与单克隆分泌模式、蛋白尿和副蛋白尿类型进行比较。
研究组包括25例MM合并严重RF患者;其中22例行计划性血液透析。对所有患者进行血清和尿液蛋白质的免疫化学研究、肾穿刺活检及其标本的光镜、免疫荧光和电子显微镜检查。
管型肾病(CN)是MM合并严重RF患者最常见的肾损害类型。32%的病例中发现CN合并单克隆免疫球蛋白沉积病。在混合性病变中,CN是急性和慢性RF发生发展的决定因素。16%的病例中发现了罕见的肾病类型,如纤维性肾小球肾炎、免疫触须样肾病和结晶性组织细胞增多症。在大多数情况下,MM患者的严重RF发生于单克隆分泌水平较低时。然而,与其他肾脏病变类型相比,CN中分泌和排泄的单克隆轻链数量更多。尿中副蛋白G的排泄提示肾小球滤过膜受损。大多数病例中检测到足细胞的退行性改变及其小突起减少。在肾小球性或混合性蛋白尿中,肾小球基底膜也存在无定形和有组织的沉积物。
肾病类型不能决定化疗后的肾脏反应。MM中CN的可逆性取决于间质纤维化程度和足细胞变化。足细胞的明显变化,如小突起减少,是化疗后肾脏反应不佳的标志。