Successful treatment with tocilizumab for refractory anemia and slowly progressive renal glomerulosclerosis in multicentric Castleman disease: A case report

RATIONALE: Multicentric Castleman disease (MCD) is a rare lymphoproliferative disorder accompanied by systemic symptoms characterized by polyclonal hypergammaglobulinemia and chronic inflammation due to overexpression of interleukin-6. Histological heterogeneity of renal involvement in MCD has been...

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Detalles Bibliográficos
Autores principales: Sugawara, Eri, Sato, Taiki, Amasaki, Yoshiharu, Katsumata, Kazuaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
6900
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878775/
https://www.ncbi.nlm.nih.gov/pubmed/35212301
http://dx.doi.org/10.1097/MD.0000000000028941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878775/
https://www.ncbi.nlm.nih.gov/pubmed/35212301
http://dx.doi.org/10.1097/MD.0000000000028941

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