234 research outputs found

    L'hyperémésis gravidarum : portrait psychodynamique de trois femmes atteintes de ce trouble rare de la grossesse

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    La prĂ©sente recherche explore l'expĂ©rience des femmes enceintes atteintes d'un trouble rare de la grossesse du nom d'hyperĂ©mĂ©sis gravidarum dont les principaux symptĂŽmes sont des nausĂ©es et des vomissements sĂ©vĂšres que la mĂ©decine parvient difficilement Ă  contrĂŽler et Ă  traiter efficacement. Cette recherche s'inscrit dans une visĂ©e exploratoire et pour cette raison utilise un devis de recherche qualitative dont la thĂ©orie de base est la thĂ©orie psychodynamique. Cette recherche a Ă©tĂ© entreprise suite au constat du peu d'intĂ©rĂȘt portĂ© aux aspects psychologiques dans le dĂ©veloppement de cette affection, les principaux Ă©crits Ă©tant de nature mĂ©dicale et par consĂ©quent s'intĂ©ressant davantage aux diffĂ©rents aspects physiologiques de ce trouble. Une question s'est alors imposĂ©e : que peut-on comprendre de cette affection de la grossesse sur le plan psychologique? Au plan thĂ©orique, la recherche s'est principalement inspirĂ©e des Ă©crits de Monique Bydlowski sur la grossesse comme crise maturative et les transformations psychiques rĂ©sultantes. D'autres auteurs dont S. Freud, F. Ferraro et A. Nunziante-Cesaro, C. Revault d'Allonnes, L. Roegiers, J-M. Delassus et C. Lechartier-Atlan ont Ă©galement enrichi le contexte thĂ©orique sur les diffĂ©rents enjeux, Ă  la fois conscients et inconscients, entourant cet Ă©vĂ©nement que reprĂ©sente la grossesse. Deux recherches portant spĂ©cifiquement sur ce trouble, soient celle de Cohen et al (2007) et de Karpel et de Gmeline (2004) ont, par ailleurs, servi de rĂ©fĂ©rence Ă  cette Ă©tude. Des entrevues individuelles semi-dirigĂ©es ont Ă©tĂ© menĂ©es Ă  deux reprises auprĂšs de trois femmes enceintes souffrant d'hyperĂ©mĂ©sis gravidarum et un inventaire de personnalitĂ©, le MMPI-II a Ă©galement Ă©tĂ© utilisĂ© afin de diversifier le matĂ©riel recueilli. L'analyse des donnĂ©es a Ă©tĂ© effectuĂ©e Ă  partir du discours de ces femmes. Celle-ci s'est inspirĂ©e de la mĂ©thode d'analyse thĂ©matique de PaillĂ©e et Mucchielli (2003). Cette analyse a donnĂ© naissance Ă  un arbre thĂ©matique composĂ© de quatorze thĂšmes descriptifs et cinq rubriques : l'univers relationnel, la maladie, la grossesse, les reprĂ©sentations des rĂŽles parentaux et la culpabilitĂ©. À chacune de ses rubriques sont rattachĂ©s les thĂšmes descriptifs. Par la suite une analyse dynamique des thĂšmes a permis d'ouvrir sur la discussion clinique et sur l'essai d'interprĂ©tation clinique, celle-ci Ă©tant inspirĂ©e des diffĂ©rents concepts psychanalytiques Ă©voquĂ©s dans la section thĂ©orique. La discussion a permis de mettre en lumiĂšre diffĂ©rentes hypothĂšses, dont celles d'Ă©ventuels manques au niveau du holding de ces femmes par leurs mĂšres, ainsi que la possibilitĂ© de recourir Ă  la grossesse marquĂ©e de l'hyperĂ©mĂ©sis gravidarum comme une tentative de recrĂ©er ce lien pourtant dĂ©cevant avec la mĂšre. \ud ______________________________________________________________________________ \ud MOTS-CLÉS DE L’AUTEUR : hyperĂ©mĂ©sis gravidarum, grossesse, conflit psychique, relation Ă  la mĂšre, ambivalence

    Hepatobiliary Cystadenoma Revealed by a Jaundice: A Case Report

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    Introduction. Hepatobiliary cystadenomas are rare benign cystic tumors and have a potential for recurrence and malignant transformation. The diagnosis may be very difficult because of absence of typical imaging feature in some cases. Case Presentation. In this paper, the authors discuss a 57-year-old woman who presented a jaundice related to hepatobiliary cystadenoma. Biological and radiological examinations have led to surgery, and the diagnosis is made after a histological examination of surgical specimens. Conclusion. This observation illustrates a hepatobiliary cystadenoma revealed by jaundice. Histology examination contributed to diagnosis. The authors discussed the mechanisms of biliary obstruction and differential diagnoses through a review of the literature

    Differentiation of hepatocellular adenoma by subtype and hepatocellular carcinoma in non-cirrhotic liver by fractal analysis of perfusion MRI

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    Background: To investigate whether fractal analysis of perfusion differentiates hepatocellular adenoma (HCA) subtypes and hepatocellular carcinoma (HCC) in non-cirrhotic liver by quantifying perfusion chaos using four-dimensional dynamic contrast-enhanced magnetic resonance imaging (4D-DCE-MRI). Results: A retrospective population of 63 patients (47 female) with histopathologically characterized HCA and HCC in non-cirrhotic livers was investigated. Our population consisted of 13 hepatocyte nuclear factor (HNF)-1 alpha-inactivated (H-HCAs), 7 beta-catenin-exon-3-mutated (b(ex3)-HCAs), 27 inflammatory HCAs (I-HCAs), and 16 HCCs. Four-dimensional fractal analysis was applied to arterial, portal venous, and delayed phases of 4D-DCE-MRI and was performed in lesions as well as remote liver tissue. Diagnostic accuracy of fractal analysis was compared to qualitative MRI features alone and their combination using multi-class diagnostic accuracy testing including kappa-statistics and area under the receiver operating characteristic curve (AUC). Fractal analysis allowed quantification of perfusion chaos, which was significantly different between lesion subtypes (multi-class AUC = 0.90, p < 0.001), except between I-HCA and HCC. Qualitative MRI features alone did not allow reliable differentiation between HCA subtypes and HCC (kappa = 0.35). However, combining qualitative MRI features and fractal analysis reliably predicted the histopathological diagnosis (kappa = 0.89) and improved differentiation of high-risk lesions (i.e., HCCs, b(ex3)-HCAs) and low-risk lesions (H-HCAs, I-HCAs) from sensitivity and specificity of 43% (95% confidence interval [CI] 23-66%) and 47% (CI 32-64%) for qualitative MRI features to 96% (CI 78-100%) and 68% (CI 51-81%), respectively, when adding fractal analysis. Conclusions: Combining qualitative MRI features with fractal analysis allows identification of HCA subtypes and HCCs in patients with non-cirrhotic livers and improves differentiation of lesions with high and low risk for malignant transformation

    EASL-ERN position paper on liver involvement in patients with Fontan-type circulation

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    Fontan-type surgery is the final step in the sequential palliative surgical treatment of infants born with a univentricular heart. The resulting long-term haemodynamic changes promote liver damage, leading to Fontan-associated liver disease (FALD), in virtually all patients with Fontan circulation. Owing to the lack of a uniform definition of FALD and the competitive risk of other complications developed by Fontan patients, the impact of FALD on the prognosis of these patients is currently debatable. However, based on the increasing number of adult Fontan patients and recent research interest, the European Association for The Study of the Liver and the European Reference Network on Rare Liver Diseases thought a position paper timely. The aims of the current paper are: (1) to provide a clear definition and description of FALD, including clinical, analytical, radiological, haemodynamic, and histological features; (2) to facilitate guidance for staging the liver disease; and (3) to provide evidence- and experience-based recommendations for the management of different clinical scenarios.</p

    EASL-ERN position paper on liver involvement in patients with Fontan-type circulation

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    Fontan-type surgery is the final step in the sequential palliative surgical treatment of infants born with a univentricular heart. The resulting long-term haemodynamic changes promote liver damage, leading to Fontan-associated liver disease (FALD), in virtually all patients with Fontan circulation. Owing to the lack of a uniform definition of FALD and the competitive risk of other complications developed by Fontan patients, the impact of FALD on the prognosis of these patients is currently debatable. However, based on the increasing number of adult Fontan patients and recent research interest, the European Association for The Study of the Liver and the European Reference Network on Rare Liver Diseases thought a position paper timely. The aims of the current paper are: (1) to provide a clear definition and description of FALD, including clinical, analytical, radiological, haemodynamic, and histological features; (2) to facilitate guidance for staging the liver disease; and (3) to provide evidence- and experience-based recommendations for the management of different clinical scenarios.</p

    Monoacylglycerol lipase reprograms hepatocytes and macrophages to promote liver regeneration

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    Background &amp; Aims: Liver regeneration is a repair process in which metabolic reprogramming of parenchymal and inflammatory cells plays a major role. Monoacylglycerol lipase (MAGL) is an ubiquitous enzyme at the crossroad between lipid metabolism and inflammation. It converts monoacylglycerols into free fatty acids and metabolises 2-arachidonoylglycerol into arachidonic acid, being thus the major source of pro-inflammatory prostaglandins in the liver. In this study, we investigated the role of MAGL in liver regeneration. Methods: Hepatocyte proliferation was studied in vitro in hepatoma cell lines and ex vivo in precision-cut human liver slices. Liver regeneration was investigated in mice treated with a pharmacological MAGL inhibitor, MJN110, as well as in animals globally invalidated for MAGL (MAGL-/-) and specifically invalidated in hepatocytes (MAGLHep-/-) or myeloid cells (MAGLMye-/-). Two models of liver regeneration were used: acute toxic carbon tetrachloride injection and two-thirds partial hepatectomy. MAGLMye-/- liver macrophages profiling was analysed by RNA sequencing. A rescue experiment was performed by in vivo administration of interferon receptor antibody in MAGLMye-/- mice. Results: Precision-cut human liver slices from patients with chronic liver disease and human hepatocyte cell lines exposed to MJN110 showed reduced hepatocyte proliferation. Mice with global invalidation or mice treated with MJN110 showed blunted liver regeneration. Moreover, mice with specific deletion of MAGL in either hepatocytes or myeloid cells displayed delayed liver regeneration. Mechanistically, MAGLHep-/- mice showed reduced liver eicosanoid production, in particular prostaglandin E2 that negatively impacts on hepatocyte proliferation. MAGL inhibition in macrophages resulted in the induction of the type I interferon pathway. Importantly, neutralising the type I interferon pathway restored liver regeneration of MAGLMye-/- mice. Conclusions: Our data demonstrate that MAGL promotes liver regeneration by hepatocyte and macrophage reprogramming. Impact and Implications: By using human liver samples and mouse models of global or specific cell type invalidation, we show that the monoacylglycerol pathway plays an essential role in liver regeneration. We unveil the mechanisms by which MAGL expressed in both hepatocytes and macrophages impacts the liver regeneration process, via eicosanoid production by hepatocytes and the modulation of the macrophage interferon pathway profile that restrains hepatocyte proliferation.The authors thank V. Fauveau, Institut Cochin, for help in surgery experiments; Olivier Thibaudeau of the Plateau de Morphologie Facility (INSERM UMR 1152, France) and Nicolas Sorhaindo of the Plateforme de Biochimie (CRI, INSERM UMR1149) for their help in the histology and liver function tests; and K. Bailly from the cytometry platform of Cochin Institute and H. Fohrer-Ting from the Centre de Recherche des Cordeliers, Paris University, for cell sorting analyses.Scopu

    Verbal and Visual Memory Impairments Among Young Offspring and Healthy Adult Relatives of Patients With Schizophrenia and Bipolar Disorder: Selective Generational Patterns Indicate Different Developmental Trajectories

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    Objective: Memory deficits have been shown in patients affected by schizophrenia (SZ) and bipolar (BP)/mood disorder. We recently reported that young high-risk offspring of an affected parent were impaired in both verbal episodic memory (VEM) and visual episodic memory (VisEM). Understanding better the trajectory of memory impairments from childhood to adult clinical status in risk populations is crucial for early detection and prevention. In multigenerational families densely affected by SZ or BP, our aim was to compare the memory impairments observed in young nonaffected offspring with memory functioning in nonaffected adult relatives and patients. Methods: For 20 years, we followed up numerous kindreds in the Eastern Québec population. After having characterized the Diagnostic and Statistical Manual of Mental Disorders phenotypes, we assessed cognition (N = 381) in 3 subsamples in these kindreds and in controls: 60 young offspring of a parent affected by SZ or BP, and in the adult generations, 92 nonaffected adult relatives and 40 patients affected by SZ or BP. VEM was assessed with the California Verbal Learning Test and VisEM with the Rey figures. Results: The VEM deficits observed in the offspring were also found in adult relatives and patients. In contrast, the VisEM impairments observed in the young offspring were present only in patients, not in the adult relatives. Conclusion: Implications for prevention and genetic mechanisms can be drawn from the observation that VEM and VisEM would show distinct generational trajectories and that the trajectory associated with VisEM may offer a better potential than VEM to predict future risk of developing the disease
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