📇 Rhumatologue · BESANCON · (25) · Salarié
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Praticien-chercheur
7 articles scientifiques publiés — formation continue solide
Disponibilité géographique
7 lieux d'exercice — choisissez celui qui vous arrange
Délais de RDV courts dans la région
118.3 rhumatos / 100 000 hab. — département bien doté
✨ Génération du profil synthétique IA en cours…
CIMRAD
CLINIQUE SAINT VINCENT CABINET DE RADIOLOGIE 40 CHEMIN DES TILLEROYES, 25000 BESANCON
CIMRAD
CENTRE D'IMAGERIE DU BOWLING 4 ROUTE DE MARCHAUX, 25000 BESANCON
CIMRAD
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
5 ROUTE DE FRANOIS, 25000 BESANCON
CIMRAD
GH HAUTE-SAONE SITE GRAY GCS IMAGERIE MEDICALE GRAY 1 RUE DE L ARSENAL BP 155, 70104 GRAY CEDEX
CIMRAD
CIT 4 CENTRE D'IMAGERIE DES TILLEROYES 4 4 RUE MADELEINE BRES, 25000 BESANCON
CIMRAD
CIT 6 CENTRE D'IMAGERIE DES TILLEROYES 6 6 RUE MADELEINE BRES, 25000 BESANCON
CIMRAD
CABINET DE RADIOLOGIE 22 RUE DES 2 PRINCESSES, 25000 BESANCON
Secteur de conventionnement non disponible (médecin hospitalier ou non présent dans l'Annuaire santé CNAM des libéraux conventionnés).
Lien Doctolib = recherche Google site:doctolib.fr (le 1er résultat est presque toujours le profil correct s'il existe).
AJR. American journal of roentgenology · 2006
The Journal of clinical endocrinology and metabolism · 2014
Background: McCune-Albright syndrome (MAS), which includes polycystic fibrous dysplasia, precocious puberty, and café au lait spots, is a rare disorder caused by somatic activating mutations of the GNAS gene. GNAS mutations have also been implicated in various sporadic tumors, including hepatobiliary and pancreatic neoplasms. Aim: The aim of this study was to assess the prevalence of hepatobiliary and pancreatic neoplasms in patients with McCune-Albright syndrome. Patients and Methods: Nineteen patients diagnosed between 1995 and 2012 with MAS in a tertiary referral center for rare growth disorders were screened with dedicated gadolinium-enhanced magnetic resonance imaging for hepatobiliary and pancreatic neoplasms between June 2011 and December 2012. Results: Six (32%) of the 19 screened patients were found to have hepatic, pancreatic, or biliary lesions, excluding liver hemangiomas, liver cysts, and focal nodular hyperplasia. This includes pancreatic ductal lesions observed in 4 patients, including numerous branch-duct intraductal papillary mucinous neoplasms in 3 patients. Biliary lesions were observed in 1 patient, with a large choledochal cyst also involving the left biliary branch. Finally, multiple inflammatory/telangiectatic hepatic adenomas were observed in 2 patients, including 1 with proven somatic GNAS mutation. Conclusion: We describe the first observation of syndromic intraductal papillary mucinous neoplasms and the new association between MAS and pancreatic neoplasms, namely intraductal papillary mucinous neoplasms of the pancreas but also rare hepatobiliary neoplasms including liver adenomas and choledochal cysts. These findings strongly suggest that somatic activating GNAS mutations, possibly through cAMP pathway disorders, are involved in the tumorigenesis of hepatobiliary and pancreatic tissues originating from the foregut endoderm and have led us to use a routine screening by dedicated magnetic resonance imaging including both pancreatobiliary and liver sequences in patients with MAS.
Liver international : official journal of the International Association for the Study of the Liver · 2007
AbstractAims/Backgrounds: Large spontaneous portal‐systemic shunts can occasionally be the cause of chronic and disabling encephalopathy in cirrhotic patients. Shunt embolization has been proposed, however the clinical relevance of this technique remains uncertain.Methods/Results: We report our results in seven patients treated by shunt embolization. Although the procedure was achieved and technically successful in all patients, the clinical results were poor as long‐term improvement was obtained in only one patient. Three patients died within 3 months after the procedure from cirrhoses' end stage complications.Conclusion: We believe that optimal management of these patients with chronic spontaneous encephalopathy is liver transplantation.
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
The Journal of clinical endocrinology and metabolism · 2014 · Journal Article
Gaujoux S, Salenave S, Ronot M, Rangheard AS, et al.
Liver international : official journal of the International Association for the Study of the Liver · 2007 · Journal Article
Zidi SH, Zanditenas D, Gelu-Siméon M, Rangheard AS, et al.
Gastroenterologie clinique et biologique · 2007 · Case Reports
Le Baleur Y, Dhalluin-Venier V, Thirot-Bidault A, Rangheard AS, et al.
AJR. American journal of roentgenology · 2006 · Comparative Study
Brillet PY, Paradis V, Brancatelli G, Rangheard AS, et al.
Gastroenterologie clinique et biologique · 2005 · Case Reports
Costes L, Thirot-Bidault A, Dhalluin-Venier V, Rangheard AS, et al.
American journal of respiratory and critical care medicine · 2004 · Case Reports
Mal H, Guignabert C, Thabut G, d'Ortho MP, et al.
AJR. American journal of roentgenology · 2002 · Journal Article
Rangheard AS, Vilgrain V, Audet P, O'Toole D, et al.