Other formats:
BibTeX
LaTeX
RIS
@article{1454376,
author = {Abla, Oussama and Jacobsen, Eric and Picarsic, Jennifer and Křenová, Zdenka and Jaffe, Ronald and Emile, JeanandFrancois and Durham, Benjamin H. and Braier, Jorge and Charlotte, Frederic and Donadieu, Jean and CohenandAubart, Fleur and RodriguezandGalindo, Carlos and Allen, Carl and Whitlock, James A. and Weitzman, Sheila and McClain, Kenneth L. and Haroche, Julien and Diamond, Eli L.},
article_location = {Washington},
article_number = {26},
doi = {http://dx.doi.org/10.1182/blood-2018-03-839753},
keywords = {Rosai-Dorfman-Destombes disease},
language = {eng},
issn = {0006-4971},
journal = {Blood},
title = {Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease},
volume = {131},
year = {2018}
}
TY - JOUR
ID - 1454376
AU - Abla, Oussama - Jacobsen, Eric - Picarsic, Jennifer - Křenová, Zdenka - Jaffe, Ronald - Emile, Jean-Francois - Durham, Benjamin H. - Braier, Jorge - Charlotte, Frederic - Donadieu, Jean - Cohen-Aubart, Fleur - Rodriguez-Galindo, Carlos - Allen, Carl - Whitlock, James A. - Weitzman, Sheila - McClain, Kenneth L. - Haroche, Julien - Diamond, Eli L.
PY - 2018
TI - Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease
JF - Blood
VL - 131
IS - 26
SP - 2877-2890
EP - 2877-2890
PB - American Society of Hematology
SN - 00064971
KW - Rosai-Dorfman-Destombes disease
N2 - Rosai-Dorfman-Destombes disease (RDD) is a rare non-Langerhans cell histiocytosis characterized by accumulation of activated histiocytes within affected tissues. RDD, which now belongs to the R group of the 2016 revised histiocytosis classification, is a widely heterogeneous entity with a range of clinical phenotypes occurring in isolation or in association with autoimmune or malignant diseases. Recent studies have found NRAS, KRAS, MAP2K1, and ARAF mutations in lesional tissues, raising the possibility of a clonal origin in some forms of RDD. More than 1000 reports have been published in the English literature; however, there is a lack of consensus regarding approach for the clinical management of RDD. Although in most cases RDD can be observed or treated with local therapies, some patients with refractory or multifocal disease experience morbidity and mortality. Here we provide the first consensus multidisciplinary recommendations for the diagnosis and management of RDD. These recommendations were discussed at the 32nd Histiocyte Society Meeting by an international group of academic clinicians and pathologists with expertise in RDD. We include guidelines for clinical, laboratory, pathologic, and radiographic evaluation of patients with RDD together with treatment recommendations based on clinical experience and review of the literature.
ER -
ABLA, Oussama, Eric JACOBSEN, Jennifer PICARSIC, Zdenka KŘENOVÁ, Ronald JAFFE, Jean-Francois EMILE, Benjamin H. DURHAM, Jorge BRAIER, Frederic CHARLOTTE, Jean DONADIEU, Fleur COHEN-AUBART, Carlos RODRIGUEZ-GALINDO, Carl ALLEN, James A. WHITLOCK, Sheila WEITZMAN, Kenneth L. MCCLAIN, Julien HAROCHE and Eli L. DIAMOND. Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease. \textit{Blood}. Washington: American Society of Hematology, 2018, vol.~131, No~26, p.~2877-2890. ISSN~0006-4971. Available from: https://dx.doi.org/10.1182/blood-2018-03-839753.
|
