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单克隆免疫球蛋白沉积病及相关疾病

Monoclonal Immunoglobulin Deposition Disease and Related Diseases.

作者信息

Kanzaki Go, Okabayashi Yusuke, Nagahama Kiyotaka, Ohashi Ryuji, Tsuboi Nobuo, Yokoo Takashi, Shimizu Akira

机构信息

Department of Analytic Human Pathology, Nippon Medical School.

Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine.

出版信息

J Nippon Med Sch. 2019;86(1):2-9. doi: 10.1272/jnms.JNMS.2019_86-1.

Abstract

Abnormal proliferation of plasma cells and some monoclonal B cells frequently cause the secretion of monoclonal immunoglobulins or immunoglobulin fragments into the serum, causing monoclonal gammopathy, which leads to various diseases including renal diseases. Therefore, monoclonal gammopathy is frequently associated with kidney diseases, including glomerular and tubulointerstitial diseases. Glomerular disease, with the deposition of monoclonal immunoglobulins or their components, includes monoclonal immunoglobulin deposition disease (MIDD), AL or AH amyloidosis, type I cryoglobulinemia, proliferative glomerulonephritis with monoclonal IgG deposits (PGNMID), immunotactoid glomerulopathy, and fibrillary glomerulonephritis. In addition, tubulointerstitial diseases with the deposition of monoclonal immunoglobulins or their components are constituted by light chain (myeloma) cast nephropathy, light chain associated Fanconi's syndrome (light chain proximal [crystal] tubulopathy), and crystal-storing histiocytosis. In the present review article, we demonstrate the clinicopathological characteristics of MIDD, which is one of the representative diseases of plasma cell dyscrasias, and discuss various renal diseases with the deposition of monoclonal immunoglobulins or their components in glomeruli and the tubulointerstitium. We recommend that these renal diseases are arranged as one disease category, "renal diseases with deposition of monoclonal immunoglobulins or their components", in order to simplify the understanding of complicated diseases in plasma cell dysplasia.

摘要

浆细胞和一些单克隆B细胞的异常增殖常常导致单克隆免疫球蛋白或免疫球蛋白片段分泌到血清中,引起单克隆丙种球蛋白病,进而导致包括肾脏疾病在内的各种疾病。因此,单克隆丙种球蛋白病常与肾脏疾病相关,包括肾小球疾病和肾小管间质疾病。伴有单克隆免疫球蛋白或其成分沉积的肾小球疾病包括单克隆免疫球蛋白沉积病(MIDD)、AL或AH淀粉样变性、I型冷球蛋白血症、伴单克隆IgG沉积的增殖性肾小球肾炎(PGNMID)、免疫触须样肾小球病和纤维样肾小球肾炎。此外,伴有单克隆免疫球蛋白或其成分沉积的肾小管间质疾病由轻链(骨髓瘤)管型肾病、轻链相关范科尼综合征(轻链近端[晶体]肾小管病)和贮晶组织细胞增多症构成。在本综述文章中,我们阐述了MIDD的临床病理特征,MIDD是浆细胞发育异常的代表性疾病之一,并讨论了伴有单克隆免疫球蛋白或其成分沉积于肾小球和肾小管间质的各种肾脏疾病。我们建议将这些肾脏疾病归为一类疾病,即“伴有单克隆免疫球蛋白或其成分沉积的肾脏疾病”,以便于简化对浆细胞发育异常中复杂疾病的理解。

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