TEMPI Syndrome: Update on Clinical Features, Management, and Pathogenesis

TEMPI Syndrome: Update on Clinical Features, Management, and Pathogenesis

TEMPI (telangiectasias, elevated erythropoietin level and erythrocytosis, monoclonal gammopathy, perinephric fluid collections, and intrapulmonary shunting) syndrome is a rare and newly defined multisystemic disease, which belongs to “monoclonal gammopathy of clinical significances”. Due to its rari...

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Bibliographic Details
Main Authors: Jian Xu, Wenqi Liu, Fengjuan Fan, Bo Zhang, Fei Zhao, Yu Hu, Chunyan Sun
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-05-01
Series:Frontiers in Endocrinology
Subjects:
TEMPI syndrome
monoclonal gammopathy of clinical significance
clinical manifestations
plasma cell-directed treatment
pathogenesis
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.886961/full

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https://www.frontiersin.org/articles/10.3389/fendo.2022.886961/full

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