TAFRO Syndrome with Renal Thrombotic Microangiopathy: Insights into the Molecular Mechanism and Treatment Opportunities

TAFRO Syndrome with Renal Thrombotic Microangiopathy: Insights into the Molecular Mechanism and Treatment Opportunities

TAFRO syndrome is an extremely rare form of idiopathic MCD, characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis on bone marrow biopsy, and organomegaly. Like idiopathic MCD, renal involvement is also a common presentation in patients with TAFRO syndrome. Furthermore, membranoproli...

Full description

Bibliographic Details
Main Authors: Kun-Hua Tu, Pei-Yi Fan, Tai-Di Chen, Wen-Yu Chuang, Chao-Yi Wu, Cheng-Lung Ku, Ya-Chung Tian, Chih-Wei Yang, Ji-Tseng Fang, Huang-Yu Yang
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:International Journal of Molecular Sciences
Subjects:
TAFRO syndrome
idiopathic multicentric Castleman disease (MCD)
IL-6
VEGF
renal thrombotic microangiopathy
Online Access:https://www.mdpi.com/1422-0067/22/12/6286

Internet

https://www.mdpi.com/1422-0067/22/12/6286

Similar Items