30 results match your criteria: "Caen Hospital[Affiliation]"

Review of definition and treatment of upper rectal cancer.

Surg Oncol

December 2024

Department of Digestive, Oncological, Endocrine, Hepatobiliary and Liver Transplant, Trousseau Hospital, University Hospital of Tours, France. Electronic address:

While the treatment of locally advanced lower and middle rectal cancer with total mesorectal excision (TME) after neoadjuvant therapy is now well defined, the treatment of locally advanced upper rectal cancer (LAURC) remains controversial. Although most teams and academic societies recommend upfront surgery (US) with partial mesorectal excision (PME), as this appears to be sufficient for these tumors, the literature remains conflicting regarding the additional use of neoadjuvant therapy and TME. Current recommendations for the treatment of LAURC do not reflect actual clinical practice.

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Nailfold capillaroscopy in acrocyanosis among patients with associated Raynaud's phenomenon.

Ann Dermatol Venereol

September 2024

Department of Dermatology, Vascular Medicine and Allergology, Tenon Hospital, Assistance Publique-Hôpitaux de Paris, 4 rue de la Chine, F-75020 Paris, France.

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Article Synopsis
  • Pathogenic variants in KMT5B, a lysine methyltransferase, are linked to global developmental issues, macrocephaly, autism, and other congenital anomalies, but the disorder is still not fully understood.
  • A study examining 43 patients revealed new significant features like hypotonia and congenital heart defects not previously associated with this condition.
  • Research using patient cell lines and KMT5B knockout mice showed that these variants lead to slow growth and highlighted alterations in pathways related to nervous system development, enhancing our understanding of the disorder's molecular mechanisms.
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RACCE Study: Impact of an enhanced recovery after surgery program (ERAS) in the management of endometrial cancer: A single-center retrospective study.

J Gynecol Obstet Hum Reprod

March 2023

Service de Gynécologie et d'Obstétrique, CHU Caen, 1 avenue de la côte de Nacre, F-14033 Caen, France; Université Caen Normandie, Esplanade de la Paix, CS 14032, F-14032 Caen, France; Unité INSERM ANTICIPE, Centre François Baclesse, 3 Ave du Général Harris, BP 5026, F-14076 Caen, France. Electronic address:

Objective: This study evaluates the implementation of an ERAS program in the gynecological surgery department of Caen University Hospital and its impact on the management of endometrial cancer. The objective was to show its impact on the length of hospitalization of patients before and after its implementation.

Patients And Method: We conducted a retrospective study including all women treated surgically for endometrial cancer at Caen University Hospital between January 1, 2015 and December 31, 2021.

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Towards an evolution in ambulatory surgery for orbital floor repair? Our experience over a period of 11 years.

J Stomatol Oral Maxillofac Surg

November 2022

Department of Maxillofacial and Plastic Surgery, Caen University Hospital 14000 Caen, France; Normandie Univ, Unicaen, Bioconnect, 14000 Caen, France; Medecine Faculty of Caen, University of Caen Basse Normandie, 14032 Caen Cedex 5, France.

Introduction: Orbital floor fracture repair is a complex surgery with intra-orbital hematoma being the most feared complication as it can lead to visual loss if not treated in good time. This is why currently patients are monitored for almost 48 hours as inpatients. The purpose of this study was to find out if orbital floor repair surgery could be safely undertaken as a day case by reviewing the experience of the last 11 years at the Caen University Hospital.

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Influence of early identification and therapy on long-term outcomes in early-onset MTHFR deficiency.

J Inherit Metab Dis

July 2022

Department of Pediatrics, Reference Center for Inborn Error of Metabolism, Necker and Robert-Debré Hospital, APHP, Université Paris Cité, Paris, France.

Article Synopsis
  • MTHFR deficiency is a serious genetic disorder affecting the body’s ability to process homocysteine, leading to severe neurological issues in infants and a lack of long-term outcome data for these patients.
  • This study analyzed clinical data from 72 MTHFR-deficient patients, focusing on those diagnosed before three months of age, to identify factors that predict severe neurodevelopmental problems.
  • Results showed that a significant percentage of early-onset patients had neurological symptoms, and those diagnosed before symptoms exhibited much better long-term outcomes, suggesting the importance of early newborn screening and treatment.
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Objective: To assess the risk of severe maternal outcomes among migrant women, considering both their legal status and birthplace; in Europe, migrant women, especially from sub-Saharan Africa, have higher risks of adverse maternal outcomes compared with non-migrants and legal status, a component of migrant condition, may be an important, and potentially actionable, risk factor.

Design: Prospective cohort study.

Setting: Four maternity units around Paris in 2010-12.

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Management of Immune Checkpoint Inhibitor-Induced Myocarditis: The French Working Group's Plea for a Pragmatic Approach.

JACC CardioOncol

March 2021

French Institute of Health and Medical Research 1263, National Institute of Agricultural Research, Centre for CardioVascular and Nutrition Research, Unit of Heart Failure and Valvular Heart Diseases, Department of Cardiology, University Mediterranean Centre of Cardio-Oncology, Nord Hospital, Assistance Publique-Hôpitaux de Marseille, Aix-Marseille University, Marseille, France.

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Thymic tumors are epithelial tumors arising from the anterior mediastinum and constitute 0.2-1.5% of all adult malignancies but are exceptional in pediatric population.

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The considerable progress made in the field of cancer treatment has led to a dramatic improvement in the prognosis of patients with cancer. However, toxicities resulting from these treatments represent a cost that can be harmful to short- and long-term outcomes. Adverse events affecting the cardiovascular system are one of the greatest challenges in the overall management of patients with cancer, as they can compromise the success of the optimal treatment against the tumor.

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Introduction: Microfat grafting is a well-known technique that is underutilized in dermatology. Instead of removing sclerotic tissue, microfat grafting preserves the tissue and uses stem cells for remodeling its structure into normal tissue. We performed a retrospective study of patients treated with microfat grafting for sclerotic and atrophic skin lesions and scars.

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Background: An increased risk of severe maternal morbidity and mortality has been described in migrant women, particularly in those born in sub-Saharan Africa. The mechanisms in question are poorly identified and rarely studied specifically.

Objective: To compare changes in maternal and perinatal morbidity inequalities among migrant and native women over time, between 2008 and 2014.

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Malignant transformation of presacral mass in Currarino syndrome.

Pediatr Blood Cancer

June 2019

Department of Pediatric Surgery, Paris Descartes University, Hôpital Necker Enfants-Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.

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Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome.

Eur J Med Genet

December 2018

Université Paris Descartes - Sorbonne Paris Cités, France; Institut Imagine-INSERM UMR-1163, Embryology and genetics of congenital malformations, France; Pediatric Neurology, Necker Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France. Electronic address:

Objectives: Periventricular nodular heterotopia (PNH) is a malformation of cortical development which presents with heterogeneous imaging, neurological phenotype and outcome. There is a paucity of comprehensive description detailing the prenatal diagnosis of PNH. The aim of this study is to report neuroimaging features and correlated outcomes in order to delineate the spectrum of prenatally diagnosed PNH.

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Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations.

Brain Dev

October 2018

Centre de Référence Déficience Intellectuelle de Causes Rares, Paris, France; APHP, Service de Neurologie Pédiatrique, Hôpital Armand Trousseau, Paris, France; APHP, Centre de Référence des Mouvements Anormaux de l'Enfant, Hôpital Armand Trousseau, Paris, France; Sorbonne Université, GRC n°19, Pathologies Congénitales du Cervelet-LeucoDystrophies, AP-HP, Hôpital Armand Trousseau, F-75012 Paris, France. Electronic address:

Objective: Heterozygous mutations in the ATP1A3 gene are responsible for various neurological disorders, ranging from early-onset alternating hemiplegia of childhood to adult-onset dystonia-parkinsonism. Next generation sequencing allowed the description of other phenotypes, including early-onset epileptic encephalopathy in two patients. We report on three more patients carrying ATP1A3 mutations with a close phenotype and discuss the relationship of this phenotype to alternating hemiplegia of childhood.

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Efficacy and safety of golimumab in Crohn's disease: a French national retrospective study.

Aliment Pharmacol Ther

December 2017

Saint Antoine Hospital, Assistance Publique des Hôpitaux de Paris (APHP), CHU, Paris, France.

Background: Anti-tumour necrosis factor (TNF) agents have improved the care of Crohn's disease (CD). After the first anti-TNF discontinuation, it is possible to switch to another anti-TNF. Three anti-TNF agents are available for ulcerative colitis (infliximab, adalimumab and golimumab), but only the first 2 have been approved for CD because golimumab has not been studied for this indication.

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Background: Phosphomannomutase 2-congenital disorder of glycosylation (PMM2-CDG) is a multisystem inborn error of metabolism.

Objectives: To better characterise the natural history of PMM2-CDG.

Methods: Medical charts of 96 patients with PMM2-CDG (86 families, 41 males, 55 females) were retrospectively reviewed.

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Child dermoid cyst mimicking a craniopharyngioma: the benefit of MRI T2-weighted diffusion sequence.

Childs Nerv Syst

February 2018

Department of Pediatric Neurosurgery, Necker Hospital, Université René Descartes, Paris Cité Sorbonne, Paris, France.

Background: Brain dermoid cysts are very rare lesions. Although benign, these cysts may be associated with devastating complications due to mass effect or meningitis. The discovery of completely asymptomatic dermoid cysts in the pediatric population is exceedingly rare.

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Low-Cost Training Simulator for Open Dismembered Pyeloplasty: Development and Face Validation.

J Surg Educ

November 2018

Department of Pediatric Surgery, Hôpital Necker-Enfants Malades, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, France; INSERM U1151, Institut Necker Enfants Malades, Hôpital Necker-Enfants Malades, Paris, France.

Purpose: Surgical simulation has benefited from a surge in interest over the last decade because of the increasing need for a change in the traditional apprenticeship model of teaching surgery. Open surgery for ureteropelvic junction (UPJ) poses unique training challenges owing to smaller workspaces, and finer sutures used that require increased surgical dexterity when compared with adult analogues. We describe the development and face validation of a low-cost training simulator for open dismembered pyeloplasty.

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The Fisher Technique for Correction of Penile Torsion in Children: Who Are the Candidates?

Urology

June 2017

Department of Pediatric Surgery, University of Caen Hospital, France; Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.

Objective: To report our experience in the treatment of penile torsion with a special reference to the Fisher technique.

Patients And Methods: We reviewed 30 cases of congenital penile torsion treated from 2009 to 2015 in a single center. Sixteen patients presented a moderate rotation of 45°-90° and 14 had a severe rotation with an angle greater than 90°.

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Management of gastric varices: a French national survey.

Eur J Gastroenterol Hepatol

May 2016

aDepartment of Hepatology, University Hospital of Besançon, Besançon bDepartment of Hepato-Gastroenterology, Purpan Hospital, Toulouse cDepartment of Hepato-Gastroenterology, La Pitié-Salpêtrière Hospital dDepartment of Hepato-Gastroenterology, Saint-Antoine Hospital, Paris eDepartment of Hepatology, Inserm U-773, Beaujon Hospital, Clichy fDepartment of Hepato-Gastroenterology, Inserm U-1075, Caen Hospital, Caen gDepartment of Hepato-Gastroenterology, Gonesse Hospital, Gonesse hDepartment of Hepatology, Saint-Joseph Hospital, Marseille iDepartment of Hepato-Gastroenterology, Angers Hospital, Angers, France.

Background And Aims: Bleeding from gastric varices is more severe than that from esophageal varices, but its management remains debated. We aimed to determine how French hepatogastroenterologists manage cirrhotic patients with gastric varices.

Methods: Hepatogastroenterologists (n=1163) working in general or university hospitals received a self-administered questionnaire.

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Hemodiafiltration Versus Hemodialysis and Survival in Patients With ESRD: The French Renal Epidemiology and Information Network (REIN) Registry.

Am J Kidney Dis

August 2016

INSERM UMRS-1018, CESP Team 5 (Renal and Cardiovascular Epidemiology), Villejuif, France; Paris Sud University, Kremlin-Bicêtre, France; Versailles Saint-Quentin University, Versailles, France.

Background: Recent randomized trials report that mortality is lower with high-convection-volume hemodiafiltration (HDF) than with hemodialysis (HD).

Study Design: We used data from the French national Renal Epidemiology and Information Network (REIN) registry to investigate trends in HDF use and its relationship with mortality in the total population of incident dialysis patients.

Setting & Participants: The study included those who initiated HD therapy from January 1, 2008, through December 31, 2011, and were dialyzed for more than 3 months; follow-up extended to the end of 2012.

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Adrenocortical tumor is a rare childhood tumor with a median age at onset of 3.2 years. Virilization is the most common sign.

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Background: Thymomas and thymic carcinomas belong to a group of thymic epithelial tumours arising from the anterior mediastinum and, are extremely rare in children in which no therapeutic guidelines have been established. The aim is to describe paediatric characteristics of these tumours and give some therapeutic indications.

Methods: Retrospective analysis of clinical data and therapeutic characteristics of paediatric patients less than 18years with thymic tumours treated between 2000 and 2012 registered in the European Cooperative Study Group for Pediatric Rare Tumors (EXPeRT) database of the cooperating national rare paediatric tumour working groups from France, Italy, Germany and Poland.

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