Erdheim-Chester disease: consensus recommendations for evaluation, diagnosis, and treatment in the molecular era

Erdheim-Chester disease (ECD) is a rare histiocytosis that was recently recognized as a neoplastic disorder owing to the discovery of recurrent activating MAPK (RAS-RAF-MEK-ERK) pathway mutations. Typical findings of ECD include central diabetes insipidus, restrictive pericarditis, perinephric fibro...

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Vydáno v:	Blood Ročník 135; číslo 22; s. 1929
Hlavní autoři:	Goyal, Gaurav, Heaney, Mark L, Collin, Matthew, Cohen-Aubart, Fleur, Vaglio, Augusto, Durham, Benjamin H, Hershkovitz-Rokah, Oshrat, Girschikofsky, Michael, Jacobsen, Eric D, Toyama, Kazuhiro, Goodman, Aaron M, Hendrie, Paul, Cao, Xin-Xin, Estrada-Veras, Juvianee I, Shpilberg, Ofer, Abdo, André, Kurokawa, Mineo, Dagna, Lorenzo, McClain, Kenneth L, Mazor, Roei D, Picarsic, Jennifer, Janku, Filip, Go, Ronald S, Haroche, Julien, Diamond, Eli L
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	United States 28.05.2020
Témata:	Clinical Trials as Topic Erdheim-Chester Disease - diagnosis Erdheim-Chester Disease - genetics Erdheim-Chester Disease - therapy Female Histiocytosis, Langerhans-Cell - diagnosis Histiocytosis, Langerhans-Cell - genetics Histiocytosis, Langerhans-Cell - therapy Humans Male MAP Kinase Signaling System - drug effects MAP Kinase Signaling System - genetics Molecular Targeted Therapy Mutation Prognosis Proto-Oncogene Proteins B-raf - antagonists & inhibitors Proto-Oncogene Proteins B-raf - genetics
ISSN:	1528-0020, 1528-0020
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