Gammopathies

0Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Hypergammaglobulinemia results from a pathologically increased production of γ globulins, that can be either mono- or polyclonal. Monoclonal gammopathy is always the consequence of a clonal B lymphocyte/plasma cell expansion with homogeneous monoclonal (M) immunoglobulin production. Diseases associated with this type of clonal proliferation are also referred to as plasma cell dyscrasia or dysproteinemias. In contrast, polyclonal gammopathy consists of a multitude of immunoglobulins produced by various stimulated B lymphocytes. It can occur in the context of lupus erythematosus, rheumatoid arthritis, sarcoidosis, Sjögren's syndrome, or chronic infections such as hepatitis B or C or acrodermatitis chronica atrophicans, as a result of repeated stimulation by an antigen. The clinical manifestations of polyclonal gammopathies are heterogeneous.

Cite

CITATION STYLE

APA

Lipsker, D., & Thomas, P. (2022). Gammopathies. In Braun-Falco’s Dermatology (pp. 1661–1669). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-662-63709-8_91

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free