54 research outputs found

    Comparison of accuracy of fibrosis degree classifications by liver biopsy and non-invasive tests in chronic hepatitis C

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    <p>Abstract</p> <p>Background</p> <p>Non-invasive tests have been constructed and evaluated mainly for binary diagnoses such as significant fibrosis. Recently, detailed fibrosis classifications for several non-invasive tests have been developed, but their accuracy has not been thoroughly evaluated in comparison to liver biopsy, especially in clinical practice and for Fibroscan. Therefore, the main aim of the present study was to evaluate the accuracy of detailed fibrosis classifications available for non-invasive tests and liver biopsy. The secondary aim was to validate these accuracies in independent populations.</p> <p>Methods</p> <p>Four HCV populations provided 2,068 patients with liver biopsy, four different pathologist skill-levels and non-invasive tests. Results were expressed as percentages of correctly classified patients.</p> <p>Results</p> <p>In population #1 including 205 patients and comparing liver biopsy (reference: consensus reading by two experts) and blood tests, Metavir fibrosis (F<sub>M</sub>) stage accuracy was 64.4% in local pathologists vs. 82.2% (p < 10<sup>-3</sup>) in single expert pathologist. Significant discrepancy (≥ 2F<sub>M </sub>vs reference histological result) rates were: Fibrotest: 17.2%, FibroMeter<sup>2G</sup>: 5.6%, local pathologists: 4.9%, FibroMeter<sup>3G</sup>: 0.5%, expert pathologist: 0% (p < 10<sup>-3</sup>). In population #2 including 1,056 patients and comparing blood tests, the discrepancy scores, taking into account the error magnitude, of detailed fibrosis classification were significantly different between FibroMeter<sup>2G </sup>(0.30 ± 0.55) and FibroMeter<sup>3G </sup>(0.14 ± 0.37, p < 10<sup>-3</sup>) or Fibrotest (0.84 ± 0.80, p < 10<sup>-3</sup>). In population #3 (and #4) including 458 (359) patients and comparing blood tests and Fibroscan, accuracies of detailed fibrosis classification were, respectively: Fibrotest: 42.5% (33.5%), Fibroscan: 64.9% (50.7%), FibroMeter<sup>2G</sup>: 68.7% (68.2%), FibroMeter<sup>3G</sup>: 77.1% (83.4%), p < 10<sup>-3 </sup>(p < 10<sup>-3</sup>). Significant discrepancy (≥ 2 F<sub>M</sub>) rates were, respectively: Fibrotest: 21.3% (22.2%), Fibroscan: 12.9% (12.3%), FibroMeter<sup>2G</sup>: 5.7% (6.0%), FibroMeter<sup>3G</sup>: 0.9% (0.9%), p < 10<sup>-3 </sup>(p < 10<sup>-3</sup>).</p> <p>Conclusions</p> <p>The accuracy in detailed fibrosis classification of the best-performing blood test outperforms liver biopsy read by a local pathologist, i.e., in clinical practice; however, the classification precision is apparently lesser. This detailed classification accuracy is much lower than that of significant fibrosis with Fibroscan and even Fibrotest but higher with FibroMeter<sup>3G</sup>. FibroMeter classification accuracy was significantly higher than those of other non-invasive tests. Finally, for hepatitis C evaluation in clinical practice, fibrosis degree can be evaluated using an accurate blood test.</p

    Hepatic Stem-like Phenotype and Interplay of Wnt/β-Catenin and Myc Signaling in Aggressive Childhood Liver Cancer

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    SummaryHepatoblastoma, the most common pediatric liver cancer, is tightly linked to excessive Wnt/β-catenin signaling. Here, we used microarray analysis to identify two tumor subclasses resembling distinct phases of liver development and a discriminating 16-gene signature. β-catenin activated different transcriptional programs in the two tumor types, with distinctive expression of hepatic stem/progenitor markers in immature tumors. This highly proliferating subclass was typified by gains of chromosomes 8q and 2p and upregulated Myc signaling. Myc-induced hepatoblastoma-like tumors in mice strikingly resembled the human immature subtype, and Myc downregulation in hepatoblastoma cells impaired tumorigenesis in vivo. Remarkably, the 16-gene signature discriminated invasive and metastatic hepatoblastomas and predicted prognosis with high accuracy

    Les tumeurs primitives neurectodermiques [i.e. neuroectodermiques] cérébrales supratentorielles (étude anatomo-clinique de 18 patients )

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    ANGERS-BU Médecine-Pharmacie (490072105) / SudocPARIS-BIUM (751062103) / SudocSudocFranceF

    Etude anatomo-clinique de 127 thrombocytémies essentielles

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    ANGERS-BU Médecine-Pharmacie (490072105) / SudocPARIS-BIUM (751062103) / SudocSudocFranceF

    Lymphome intravasculaire : à propos de deux observations autopsiques et revue de la littérature

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    International audienceIntravacular large B-cell lymphoma (LIV) is a rare entity individualized in the WHO classification since 2001&nbsp;as a subtype of extranodal diffuse large B-cell lymphoma. We report two autopsic cases of LIV: a 77-year-old woman presenting with fever, dyspnea, antehypophyseal failure and a 54-year-old man presenting with fever, weight-loss, night-sweats and encephalopathy. They died respectively 10&nbsp;and 7&nbsp;months after the beginning of symptoms, without diagnosis. Neither infectious disease nor lymphomatous proliferation had been identified. From these two cases and our literature review, we insist on the importance of histopathological diagnosis on biopsy for this rare pathology which clinical diagnosis remains difficult.Les lymphomes intravasculaires à grandes cellules B (LIV) sont rares et individualisés dans la classification de l’OMS depuis 2001&nbsp;comme un sous-type de lymphome B diffus à grandes cellules extraganglionnairea. Nous rapportons deux cas de LIV de diagnostic autopsique. Il s’agissait d’une femme de 77&nbsp;ans ayant présenté fièvre, dyspnée, insuffisance antéhypophysaire et d’un homme de 54&nbsp;ans ayant présenté fièvre, amaigrissement, sueurs nocturnes et encéphalopathie. Ils sont décédés respectivement dix et sept mois après le début des symptômes, sans diagnostic. Les bilans infectieux étaient négatifs. Aucune prolifération lymphomateuse n’avait été mise en évidence. Évoquer et diagnostiquer cliniquement un LIV est difficile car il s’agit d’une pathologie rare dont les symptômes peuvent être très variables. À partir de ces deux observations et de la revue de la littérature, nous présentons l’intérêt des différentes biopsies dans la mise en évidence de la prolifération lymphomateuse.</p

    Superficial femoral artery transposition repair for isolated superior mesenteric artery dissection

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    Isolated dissection of the superior mesenteric artery is an uncommon event, but many new cases have been reported recently, reflecting the progress of imaging and suggesting that this pathology is not as rare as previously thought. Here we report a case of superior mesenteric artery dissection where we performed, after failure of conservative medical management, an original surgical technique for mesenteric revascularization using a superficial femoral artery transposition. To the best of our knowledge, this is the first report of the use of this technique for complex mesenteric revascularization
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