Idiopathic Multicentric Castleman Disease with Strikingly Elevated IgG4 Concentration in the Serum and Abundant IgG4-Positive Cells in the Tissue: A Case Report

Idiopathic multicentric Castleman disease (iMCD) can be challenging to distinguish clinically and histopathologically from Immunoglobulin G4-related disease (IgG4RD). A 73-year-old man was referred to a rheumatologist for suspected autoimmune-related polyclonal hypergammaglobulinemia. The patient ha...

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Principais autores:	Chia-Chun Cheng, Ying-Chu Chen, Yung-Hsiang Hsu, Kuei-Ying Su
Formato:	Artigo
Idioma:	Inglês
Publicado em:	MDPI AG 2022-09-01
coleção:	Diagnostics
Assuntos:	idiopathic multicentric Castleman disease (iMCD) IgG4-related disease (IgG4RD) multiple lymphadenopathies
Acesso em linha:	https://www.mdpi.com/2075-4418/12/9/2261
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