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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Detalles Bibliográficos
Autores principales: Cheng, Chia-Chun, Chen, Ying-Chu, Hsu, Yung-Hsiang, Su, Kuei-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498249/
https://www.ncbi.nlm.nih.gov/pubmed/36140662
http://dx.doi.org/10.3390/diagnostics12092261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498249/
https://www.ncbi.nlm.nih.gov/pubmed/36140662
http://dx.doi.org/10.3390/diagnostics12092261

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