Pierre Goudet
University of Burgundy
EndocrinologySurgeryMultiple endocrine neoplasiaGeneral surgeryMedicine
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Publications 74
#1Louis de Mestier (University of Paris)H-Index: 14
#2Côme Lepage (University of Burgundy)H-Index: 31
Last. Rodica GinculH-Index: 11
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INTRODUCTION: This document is a summary of the French Intergroup guidelines regarding the management of digestive neuroendocrine neoplasms (NEN) published in February 2020 ( METHODS: All French medical societies involved in the management of NEN took part in this work. Recommendations were graded into four categories (A, B, C or D), according to the level of evidence found in the literature until May 2019. RESULTS: The management of NEN is challenging because of their heterogeneit...
#2Christine Do CaoH-Index: 13
Last. Thomas WalterH-Index: 32
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Objective:The primary endpoint was to analyze the predictive factors of lymph node involvement (LN+).Background:Indications for additional right hemicolectomy (RHC) with lymph node (LN) resection after appendectomy for appendix neuroendocrine tumor (A-NET) remain controversial, especially for tumors
4 CitationsSource
#1Pauline RomanetH-Index: 2
#2Sophie GiraudH-Index: 41
Last. Anne BarlierH-Index: 39
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#1Nathalie Chereau (University of Paris)H-Index: 8
#2Tristan GreilsamerH-Index: 4
Last. Fabrice Menegaux (University of Paris)H-Index: 27
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Abstract Background Encapsulated follicular variant of papillary thyroid carcinoma has recently been reclassified as noninvasive follicular thyroid neoplasm with papillary-like nuclear features on the basis of its highly indolent behavior, as proposed by an international group of experienced thyroid pathologists. Methods All patients from 9 high-volume endocrine surgery departments who underwent surgery between 2005 and 2015 and whose final surgical pathology revealed noninvasive follicular thyr...
2 CitationsSource
#1Pauline RomanetH-Index: 2
#2Pierre GoudetH-Index: 18
Last. Anne BarlierH-Index: 39
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#2Christine Binquet (University of Burgundy)H-Index: 34
Last. Pierre GoudetH-Index: 18
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Objective To evaluate the natural history of MEN1-related bronchial endocrine tumors (br-NETs) and to determine their histological characteristics, survival and causes of death.
4 CitationsSource
#1Samira M. SadowskiH-Index: 20
#2Guillaume CadiotH-Index: 42
Last. Frédéric TriponezH-Index: 23
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Multiple endocrine neoplasia type 1 (MEN1) is a hereditary autosomal dominant disorder associated with numerous neuroendocrine tumors (NETs). Recent advances in the management of MEN1 have led to a decrease in mortality due to excess hormones; however, they have also led to an increase in mortality from malignancy, particularly NETs. The main challenges are to localize these tumors, to select those that need therapy because of the risk of aggressive behavior, and to select the appropriate therap...
3 CitationsSource
#1Frédéric TriponezH-Index: 23
#2Samira M. SadowskiH-Index: 20
Last. Pierre GoudetH-Index: 18
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Objective:To report long-term follow-up of patients with multiple endocrine neoplasia type 1 (MEN1) and nonfunctioning pancreatic neuroendocrine tumors (NF-PET).Background:Pancreaticoduodenal tumors occur in almost all patients with MEN1 and are a major cause of death. The natural history and clinic
18 CitationsSource
#1Nathalie Chereau (UPMC: Pierre-and-Marie-Curie University)H-Index: 8
#2Xavier Giudicelli (UPMC: Pierre-and-Marie-Curie University)H-Index: 1
Last. Fabrice Menegaux (UPMC: Pierre-and-Marie-Curie University)H-Index: 27
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Context: Diffuse sclerosing variant (DSV) is a rare and aggressive subtype of papillary thyroid carcinoma (PTC). Objective: The objective of the study was to investigate the clinicopathological features and prognosis of DSV patients and compare these findings with all other PTCs and high-risk PTCs. Design and Setting: The data of patients who underwent surgery for DSV and PTC between 2003 and 2014 in seven surgical departments specialized in endocrine surgery were reviewed. Patients: Fifty-six D...
5 CitationsSource
#1Julien ThevenonH-Index: 25
#2Abderrahmane Bourredjem (French Institute of Health and Medical Research)H-Index: 6
Last. Pierre GoudetH-Index: 18
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MEN1, which is secondary to the mutation of the MEN1 gene, is a rare autosomal-dominant disease that predisposes mutation carriers to endocrine tumors. Most studies demonstrated the absence of direct genotype-phenotype correlations. The existence of a higher risk of death in the Groupe d'etude des Tumeurs Endocrines-cohort associated with a mutation in the JunD interacting domain suggests heterogeneity across families in disease expressivity. This study aims to assess the existence of modifying ...
17 CitationsSource