EMILIE BEQUIGNON

Dr. EMILIE BEQUIGNON

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2017 in International Journal of Oral and Maxillofacial Surgery
Verified
Journal Article
Closed access
RBRomain Bosc
Romain Bosc
BHB. Hersant
B. Hersant
RCRaphael Carloni
Raphael Carloni
JNJ. Niddam
J. Niddam
JBJ. Bouhassira
J. Bouhassira
JMJ.-P. Meningaud
J.-P. Meningaud

1 August 2016 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
EKElma El Khouri
Elma El Khouri
LTLucie Thomas
Lucie Thomas
LJLudovic Jeanson
Ludovic Jeanson
EBEMILIE BEQUIGNON
EMILIE BEQUIGNON
BVBenoit Vallette
Benoit Vallette
SASerge Amselem
Serge Amselem

10 April 2018 in Orphanet Journal of Rare Diseases
Verified
Journal Article
Open access
PDF file
TDThe French National Reference Center For Toxic Bullous Dermatoses
The French National Reference Center For Toxic Bullous Dermatoses
SISaskia Ingen-Housz-Oro
Saskia Ingen-Housz-Oro
TDTu-Anh Duong
Tu-Anh Duong
BBBenoit Bensaid
Benoit Bensaid
NBNathalia Bellon
Nathalia Bellon
PWPierre Wolkenstein
Pierre Wolkenstein
Epidermal necrolysis (EN) encompasses Stevens-Johnson syndrome (SJS, < 10% of the skin affected), Lyell syndrome (toxic epidermal necrolysis, TEN, with ≥30% of the skin affected) and an overlap syndrome (10 to 29% of the skin affected). These rare diseases are caused, in 85% of cases, by pharmacological treatments, with symptoms occurring 4 to 28 days after treatment initiation. Mortality is 20 to 25% during the acute phase, and almost all patients display disabling sequelae (mostly ocular impairment and psychological distress). The objective of this French national diagnosis and care protocol (protocole national de diagnostic et de soins; PNDS), based on a critical literature review and on a multidisciplinary expert consensus, is to provide health professionals with an explanation of the optimal management and care of patients with EN. This PNDS, written by the French National Reference Center for Toxic Bullous Dermatoses was updated in 2017 ( https://www.has-sante.fr/portail/jcms/c_1012735/fr/necrolyse-epidermique-syndromes-de-stevens-johnson-et-de-lyell ). The cornerstone of the management of these patients during the acute phase is an immediate withdrawal of the responsible drug, patient management in a dermatology department, intensive care or burn units used to dealing with this disease, supportive care and close monitoring, the prevention and treatment of infections, and a multidisciplinary approach to sequelae. Based on published data, it is not currently possible to recommend any specific immunomodulatory treatment. Only the culprit drug and chemically similar molecules must be lifelong contraindicated.

1 July 2018 in Journal of the American Academy of Dermatology
Verified
Journal Article
Closed access
RAReyhan Amode
Reyhan Amode
SISaskia Ingen-Housz-Oro
Saskia Ingen-Housz-Oro
NONicolas Ortonne
Nicolas Ortonne
TBTouda Bounfour
Touda Bounfour
SPSabine Pereyre
Sabine Pereyre
OCOlivier Chosidow
Olivier Chosidow

Verified
Journal Article
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FCFlorent Carsuzaa
Florent Carsuzaa
EBEMILIE BEQUIGNON
EMILIE BEQUIGNON
XDXavier Dufour
Xavier Dufour
GBGuillaume de Bonnecaze
Guillaume de Bonnecaze
JLJean-Claude Lecron
Jean-Claude Lecron
LLLaure Favot Laforge
Laure Favot Laforge
Cytokines are well known to play a central role in chronic rhinosinusitis with nasal polyps (CRSwNP), particularly in maintenance of the inflammatory response and the recruitment of eosinophils. The pathophysiological concepts concerning the involvement of inflammatory cytokines in CRSwNP have gradually evolved. Although the Th2 cytokines environment associated with an eosinophilic infiltration has retained a central role in the genesis of polyps, the role of other cytokine subpopulations has also and more recently been detailed, leading to a specific and complex signature in CRSwNP. The purpose of this review is to summarize the current state of knowledge about the cytokine signature in CRSwNP, the role of cytokines in the pathogenesis of this disease and in the intercellular dialog between epithelial cells, fibroblasts and inflammatory cells. Knowledge of this precise cytokine signature in CRSwNP is fundamental in the perspective of potential targeting biotherapies.

Verified
Journal Article
Open access
PDF file
EBEMILIE BEQUIGNON
EMILIE BEQUIGNON
LDLaurence Dupuy
Laurence Dupuy
FZFrancoise Zerah-Lancner
Francoise Zerah-Lancner
LBLaurence Bassinet
Laurence Bassinet
IHIsabelle Honoré
Isabelle Honoré
JPJean-Francois PAPON
Jean-Francois PAPON
To date, no study precisely described ear, nose and throat (ENT) disease in adults with primary ciliary dyskinesia (PCD) and its relationship with ciliary function/ultrastructure. A retrospective study of standardized ENT data (exam, audiogram, sinus Computed tomography (CT), and bacteriology) was conducted in 64 adults with confirmed PCD who were followed in two ENT reference centers. Rhinorrhoea and hearing loss were the main symptoms. Symptom scores were higher in older patients. Nasal endoscopy was abnormal in all patients except one, showing nasal polyps in one-third of the patients and stagnant nasal mucus secretions in 87.5% of the patients. Sinus CT opacities were mainly incomplete and showed one-third of the patients with sinus hypoplasia and/or agenesis. Middle meatus mainly grew Haemophilus influenzae, Streptoccocus pneumoniae and Pseudomonas aeruginosa. Otitis media with effusion (OME), which is constant in childhood, was diagnosed in less than one-quarter of the patients. In two-thirds of the patients, audiogram showed hearing loss that was sensorineural in half of the patients. ENT disease severity was not correlated with ciliary function and ultrastructure, but the presence of OME was significantly associated with a forced expiratory volume (FEV1) < 70%. Rhinosinusitis is the most common clinical feature of PCD in adults, while OME is less frequent. The presence of active OME in adults with PCD could be a severity marker of lung function and lead to closer monitoring.