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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Podrobná bibliografie
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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Popis
Shrnutí:	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 fibrosis, and sclerotic bone lesions. The histopathologic diagnosis of ECD is often challenging due to nonspecific inflammatory and fibrotic findings on histopathologic review of tissue specimens. Additionally, the association of ECD with unusual tissue tropism and an insidious onset often results in diagnostic errors and delays. Most patients with ECD require treatment, except for a minority of patients with minimally symptomatic single-organ disease. The first ECD consensus guidelines were published in 2014 on behalf of the physicians and researchers within the Erdheim-Chester Disease Global Alliance. With the recent molecular discoveries and the approval of the first targeted therapy (vemurafenib) for BRAF-V600-mutant ECD, there is a need for updated clinical practice guidelines to optimize the diagnosis and treatment of this disease. This document presents consensus recommendations that resulted from the International Medical Symposia on ECD in 2017 and 2019. Herein, we include the guidelines for the clinical, laboratory, histologic, and radiographic evaluation of ECD patients along with treatment recommendations based on our clinical experience and review of literature in the molecular era.
Bibliografie:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23
ISSN:	1528-0020 1528-0020
DOI:	10.1182/blood.2019003507