10 results match your criteria: "Centre pluridisciplinaire de diagnostic prénatal de Rennes[Affiliation]"

Management of adipose tumors in the limbs.

Orthop Traumatol Surg Res

February 2022

Service de chirurgie orthopédique et traumatologique, CHU Pontchaillou, université de Rennes 1, rue Henri-Le-Guillou, 35033 Rennes, France; Réseau HUGORTHO : réseau des services de chirurgie orthopédique et traumatologique adulte et enfant des hôpitaux universitaires du Grand Ouest, France.

Adipose tumors of the limbs are the most common soft tissue lesions and are essentially benign (lipomas). However, in some cases, they can be considered as tumors with intermediate malignancy (atypical lipomatous tumor [ALT]) or sarcoma lineage (liposarcoma [LS]). The essential work-up for a potential adipose tumor consists of a clinical examination and initial ultrasound imaging to determine the size (more or less than 5 cm), the location (over or under the fascia) and any potential atypical vascularization.

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Reassessment of the risk of birth defects due to Zika virus in Guadeloupe, 2016.

PLoS Negl Trop Dis

March 2021

Emerging Disease Epidemiology Unit, Institut Pasteur, Paris, France.

Background: In the French Territories in the Americas (FTA), the risk of birth defects possibly associated with Zika virus (ZIKV) infection was 7.0% (95%CI: 5.0 to 9.

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Myorelaxants in ARDS patients.

Intensive Care Med

December 2020

Assistance Publique - Hôpitaux de Marseille, Hôpital Nord, Médecine Intensive Réanimation, 13015, Marseille, France.

Neuromuscular blocking agents (NMBAs) inhibit patient-initiated active breath and the risk of high tidal volumes and consequent high transpulmonary pressure swings, and minimize patient/ ventilator asynchrony in acute respiratory distress syndrome (ARDS). Minimization of volutrauma and ventilator-induced lung injury (VILI) results in a lower incidence of barotrauma, improved oxygenation and a decrease in circulating proinflammatory markers. Recent randomized clinical trials did not reveal harmful muscular effects during a short course of NMBAs.

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Article Synopsis
  • Osteoarthritis (OA) is a common joint disease, and this study focuses on early-onset OA, which affects people younger than the typical age range; it examines the genetic causes specifically in individuals with nonsyndromic early-onset OA.
  • The study involved 45 patients with specific criteria, and researchers used genetic sequencing to identify variants in some patients, notably the COL2A1 gene, which was found in the majority of those with a genetic cause for their condition.
  • The findings suggest that COL2A1 is the primary genetic factor for nonsyndromic early-onset OA, and highlight the need for genetic testing in patients needing joint replacements before age 45, along with lifestyle recommendations for prevention.
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Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.

Ultrasound Obstet Gynecol

December 2018

Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France.

Objective: To determine the frequency and nature of copy number variants (CNVs) identified by chromosomal microarray analysis (CMA) in a large cohort of fetuses with isolated increased nuchal translucency thickness (NT) ≥ 3.5 mm.

Methods: This was a retrospective, multicenter study, including 11 French hospitals, of data from the period between April 2012 and December 2015.

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[Screening for pulmonary arterial hypertension in patients with systemic sclerosis: Comparison of DETECT algorithm to decisions of a multidisciplinary team, in a competence centre].

Rev Med Interne

August 2017

Service de médecine interne, hôpital Sud, CHU de Rennes, BP 90347, 16, boulevard de Bulgarie, 35203 Rennes cedex 2, France; UMR Inserm U1085, institut de recherche sur la santé, l'environnement et le travail (IRSET), université de Rennes 1, 35203 Rennes, France.

Introduction: Pulmonary arterial hypertension (PAH) is a severe complication of systemic sclerosis and detecting PAH efficiently remains challenging. The DETECT study has offered in 2013 a composite screening tool for PAH. The objective of our study was to compare the indication of right heart catheterisation (RHC) as suggested by the DETECT algorithm with the decisions of a multidisciplinary team.

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Objectives: To study the pregnancies followed at Rennes University Hospital from 2006 to 2012, after prenatal diagnosis of lethal fetal condition and prenatal project of palliative care at birth consisting of comfort care emphasizing parent-child encounters and bonding.

Material And Methods: Retrospective study of 20 pregnancies with diagnosis of lethal fetal condition where parents accepted antenatally the proposal or sought for palliative care at birth.

Results: Diagnosis was made at a median age of 20 weeks gestation (12-33).

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[Termination of pregnancy without feticide: A French national survey].

J Gynecol Obstet Biol Reprod (Paris)

June 2016

Département de gynécologie obstétrique, centre pluridisciplinaire de diagnostic prénatal, CHU de Rennes, 16, boulevard de Bulgarie, 35000 Rennes, France.

Purpose: Termination of pregnancy without feticide (TOPWF) is poorly known in France and far less practiced than palliative care after term birth of a child having a lethal pathology. Few teams consider it and its practice remains confidential. This survey tries to describe it.

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[Antenatal metastatic neuroblastoma: prognostic criteria. A case report].

J Gynecol Obstet Biol Reprod (Paris)

December 2003

Département de Gynécologie Obstétrique et Biologie de la Reproduction, CHU de Rennes, Centre Pluridisciplinaire de Diagnostique Prénatal, 2, rue de l'Hôtel-Dieu, 35000 Rennes.

Neuroblastoma, the most common malignant tumor in the neonatal period is metastatic in 25 to 50% of cases. While the prognosis of antenatal neuroblastoma is often considered as favorable, included in the most common metastatic stage (Stage IV S), it can lead to fetal or neonatal death. We report a case of a fetus with a stage IV neuroblastoma who died in utero.

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Objectives: To assess the prognosis of prenatally diagnosed congenital diaphragmatic hernia (CDH) during the years 1995-2000 in order to improve prenatal counselling.

Methods: Retrospective study of all 31 cases of women with prenatally diagnosed CDH.

Results: Nine pregnancies (29%) were terminated and two fetuses (6%) were stillborn.

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