Monoclonal Immunoglobulin Deposition Disease and Related Diseases.

glomerular deposition disease light chain deposition disease (LCDD) monoclonal gammopathy of renal significance (MGRS) monoclonal gammopathy of undetermined significance (MGUS) monoclonal immunoglobulin deposition disease (MIDD)

Journal

Journal of Nippon Medical School = Nippon Ika Daigaku zasshi
ISSN: 1347-3409
Titre abrégé: J Nippon Med Sch
Pays: Japan
ID NLM: 100935589

Informations de publication

Date de publication:
2019
Historique:
entrez: 29 3 2019
pubmed: 29 3 2019
medline: 25 4 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 30918151
doi: 10.1272/jnms.JNMS.2019_86-1
doi:

Substances chimiques

Antibodies, Monoclonal 0
Immunoglobulin G 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2-9

Auteurs

Go Kanzaki (G)

Department of Analytic Human Pathology, Nippon Medical School.
Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine.

Yusuke Okabayashi (Y)

Department of Analytic Human Pathology, Nippon Medical School.
Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine.

Kiyotaka Nagahama (K)

Department of Pathology, Kyorin University School of Medicine.

Ryuji Ohashi (R)

Department of Diagnostic Pathology, Nippon Medical School Hospital.

Nobuo Tsuboi (N)

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

Takashi Yokoo (T)

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

Akira Shimizu (A)

Department of Analytic Human Pathology, Nippon Medical School.

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Classifications MeSH