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1.
Hepatology ; 68(4): 1534-1548, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-29637581

RESUMO

Progenitor-derived regeneration gives rise to the aberrant expression of biliary markers such as cytokeratin 7 (K7) and epithelial cell adhesion molecule (EpCAM) in hepatocytes. We aimed to describe the expression of these molecules in patients with compensated hepatitis C virus (HCV)-related cirrhosis and to investigate its potential influence on cirrhosis complications. Among patients with Child-Pugh A uncomplicated HCV-related cirrhosis enrolled in the prospective ANRS CO12 CirVir cohort, we selected individuals with a liver biopsy collected within 2 years before inclusion in the study. K7 and EpCAM immunostaining identified intermediate hepatobiliary cells. The influence of biliary marker expres-sion in hepatocytes on decompensation events and the occurrence of hepatocellular carcinoma (HCC) was studied using a multivariate Cox proportional hazards regression model. Among the 337 patients eligible for the study (men, 67%; median age, 52 years), 198 (58.8%) had biopsies with K7-positive hepatocytes including extensive staining in 40 (11.9%) and 203 had EpCAM-positive hepatocytes (60.6%). During follow-up (median, 54.2 months), 47 patients (14%) experienced a decompensation event, and HCC was diagnosed in 37 patients (11%). Extensive K7 staining was independently associated with the occurrence of a decompensation event (hazard ratio [HR], 3.00; 95% confidence interval [CI], 1.30-6.89; P = 0.010). EpCAM expression was independently associated with HCC occurrence (HR, 2.37; 95% CI, 1.07-5.23; P =0.033) along with age and a low prothrombin ratio. CONCLUSION: Progenitor-derived regeneration depicted by K7 and EpCAM immunostaining of hepatocytes in liver biopsies of patients with compensated HCV-related cirrhosis marks a cirrhosis stage more prone to develop complications. (HEPATOLOGY 2018; 68:1534-1548).


Assuntos
Hepacivirus/metabolismo , Hepatite C/complicações , Queratinas/metabolismo , Cirrose Hepática/virologia , Células-Tronco/fisiologia , Adulto , Idoso , Biomarcadores/metabolismo , Biópsia por Agulha , Estudos de Coortes , Molécula de Adesão da Célula Epitelial/metabolismo , Feminino , Hepatite C/mortalidade , Hepatite C/patologia , Humanos , Imuno-Histoquímica , Cirrose Hepática/patologia , Regeneração Hepática/fisiologia , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Prognóstico , Modelos de Riscos Proporcionais , Estudos Prospectivos , Medição de Risco , Taxa de Sobrevida
2.
Ann Pathol ; 29(2): 74-9, 2009 Apr.
Artigo em Francês | MEDLINE | ID: mdl-19364576

RESUMO

AIM: To assess the reliability of systematic and exhaustive cancer Adicap code registration by French pathology laboratories within the Crisap of Paca East network. METHODS: The Adicap code includes tumour site, histology and pathology technique. A quality control programme was applied to malignant and in situ tumours with an Adicap code to assess data quality, correct errors and supply missing data, based on IARC recommendations. RESULTS: In 2005 and 2006, 45,980 pathology examinations were entered in the Crisap of Paca East database. There was at least one Adicap code per examination, patients, surgeons and pathologists were identified and date of diagnosis was completed, as recommended by the HAS-Afaqap 2005 French pathologist professional quality control. Discrepancies between histopathology tissue and tumour site were found in 0.32% of cases (n=147), between age and histopathology in 0.04% of cases (n=19), and between genital tumour and sex in 0.01% of cases (n=3). In 2006, within 9535 subjects, dates of birth and postcodes of residence were missing, respectively, in 0.39% (n=37) and 22.46% (n=2142) of cases. CONCLUSION: Data quality for the Adicap code database may be considered satisfactory. Extended to Paca in 2007, Crisap Paca database can now be exploited for Paca regional cancer control strategy.


Assuntos
Neoplasias/epidemiologia , Sistema de Registros/normas , Adolescente , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Algoritmos , Criança , Feminino , França/epidemiologia , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias/patologia , Controle de Qualidade , Reprodutibilidade dos Testes
3.
J Gastrointestin Liver Dis ; 27(4): 469-471, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30574631

RESUMO

Breast cancer metastases to the gastrointestinal tract are rare, with a median time interval from the diagnosis of the primary tumor to metastasis up to 7 years. The stomach is the most frequent metastatic site and invasive lobular carcinoma is the type with the highest affinity to the digestive system. We report the case of an 84-year-old female patient, with a past medical history 20 years earlier of invasive lobular carcinoma of the breast, who presented for dyspepsia. Upper endoscopy revealed hypertrophic gastric folds compatible with primary linitis plastica. Histology showed proliferation of malignant poorly cohesive cells. Immunohistochemistry stain showed intense positivity of estrogen receptors and anti-GATA-binding protein 3 nuclear antibodies, and absence of the human epidermal growth factor receptor 2. These findings confirmed the diagnosis of a metachronous metastasis of the invasive lobular breast adenocarcinoma. Considering metastases from breast cancer is crucial when patients with any subtle gastric symptom and a past medical history of invasive lobular adenocarcinoma of the breast seek medical advice, even though more than 20 years after primary breast cancer. Immunohistochemistry is the key to final diagnosis as these lesions can endoscopically and histologically mimic primary linitis plastica.


Assuntos
Neoplasias da Mama/patologia , Carcinoma Lobular/secundário , Linite Plástica/patologia , Neoplasias Gástricas/secundário , Idoso de 80 Anos ou mais , Antineoplásicos Hormonais/administração & dosagem , Biomarcadores Tumorais/análise , Biópsia , Neoplasias da Mama/química , Carcinoma Lobular/química , Carcinoma Lobular/tratamento farmacológico , Diagnóstico Diferencial , Feminino , Fulvestranto/administração & dosagem , Fator de Transcrição GATA3/análise , Gastroscopia , Humanos , Imuno-Histoquímica , Linite Plástica/química , Valor Preditivo dos Testes , Neoplasias Gástricas/química , Neoplasias Gástricas/tratamento farmacológico , Fatores de Tempo , Resultado do Tratamento
4.
Gastroenterol Clin Biol ; 31(5): 485-92, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17541338

RESUMO

OBJECTIVES: Certain practices with a potential risk of hepatitis C virus (HCV) transmission begin early, during adolescence. In 2004, primary prevention interventions targeting adolescents aged 13-17 years attending school in the Alpes-Maritimes region of France were conducted by the "Réseau Hépatite C Ville Hôpital Côte d'Azur". The aim of this study was to assess the adolescents' knowledge about HCV and to evaluate the impact of such interventions. METHODS: A random sample of secondary state schools in the Alpes-Maritimes was invited to participate in the study. Before and after presenting a slide show about HCV in the selected classrooms, the investigators asked the students to complete an anonymous self-administered questionnaire designed to assess their knowledge about HCV infection. RESULTS: The intervention concerned a study population of 2,946 students, mean age 14.4 +/- 2.5 years. Before the interventions, 21% had good knowledge of HCV infection and 24% had good know-ledge of disease contagion. These percentages increased significantly after the interventions to 95% and 84% respectively. Knowledge improvement was more significant among high school students and among students whose parents had an employment. CONCLUSIONS: Adolescents are poorly informed about HCV infection. The present intervention enabled significant improvement in their knowledge about the infection and disease contagion, independently of gender, age and geographical area.


Assuntos
Educação em Saúde , Hepatite C , Adolescente , Comportamento do Adolescente , Fatores Etários , Atitude Frente a Saúde , Piercing Corporal , França , Conhecimentos, Atitudes e Prática em Saúde , Hepatite C/prevenção & controle , Hepatite C/transmissão , Humanos , Assunção de Riscos , Fatores Sexuais , Classe Social , Tatuagem , Vacinas contra Hepatite Viral
5.
AIDS ; 18(16): 2163-70, 2004 Nov 05.
Artigo em Inglês | MEDLINE | ID: mdl-15577649

RESUMO

BACKGROUND: The impact of immune reconstitution on liver fibrosis in HIV/hepatitis C virus (HCV) patients is unknown. In this case-control study, we investigated the impact of HIV infection on the severity of liver fibrosis and identified related factors. METHODS: We studied 116 HIV/HCV patients and 235 HCV only patients all untreated for HCV. Each co-infected patient was matched with two singly-infected patients according to gender, age at contamination and duration of infection. Liver biopsy was analysed using the METAVIR score. RESULTS: Alcohol consumption and route of contamination differed between HCV-infected and HCV/HIV co-infected patients. Among co-infected patients, a F3-F4 Metavir score was significantly more frequent than in mono-infected patients. Co-infected patients with severe fibrosis (F3-F4) had higher transaminase, ferritin levels and lower CD4 T-cell count than patients with none to moderate fibrosis (F0-F2). Although median duration of treatment with nucleoside analogues, non-nucleoside analogues and protease inhibitors were comparable in both groups, the delay between the presumed date of contamination and treatment initiation with highly active antiretroviral therapy (HAART) was significantly longer for patients with severe fibrosis than those with none to moderate fibrosis. Finally, the mean rate of fibrosis progression was significantly slower among patients exposed to HAART. CONCLUSION: Early antiretroviral therapy in co-infected HIV-HCV patients may slow liver fibrosis progression.


Assuntos
Fármacos Anti-HIV/uso terapêutico , Infecções por HIV/virologia , Hepatite C/virologia , Cirrose Hepática/virologia , Adolescente , Adulto , Terapia Antirretroviral de Alta Atividade , Estudos de Casos e Controles , Progressão da Doença , Feminino , Infecções por HIV/patologia , Hepatite C/patologia , Humanos , Fígado/patologia , Fígado/virologia , Cirrose Hepática/patologia , Masculino , Análise de Regressão
6.
Gastroenterol Clin Biol ; 26(1): 57-61, 2002 Jan.
Artigo em Francês | MEDLINE | ID: mdl-11938041

RESUMO

OBJECTIVE: To perform a descriptive analysis of patients with chronic hepatitis C based on a local registry of liver biopsies. PATIENTS AND METHOD: Collection of clinical, biological and histological data from all HCV-infected patients who underwent liver biopsy between January 1997 and December 1998 in the Alpes-Maritimes (France). RESULTS: One thousand and fifty six patients including 924 who lived in the Alpes-Maritimes (515 male, 409 female, mean age: 44.9 years old) were included. Intravenous drug use (30.1%) was the major suspected source of infection before blood transfusion (28.2%). Among intravenous drug users, 38% of patients were infected with genotype 1a and 37.4% with genotype 3. The METAVIR fibrosis severity score was distributed as follows: F0: 10.8%, F1: 53.7%, F2: 15.9%, F3: 14.7%, and F4: 4.9%. In a multivariate analysis adjusted for the duration of infection, independent risk factors associated with the severity of fibrosis were age at contamination >=30 years, genotype other than 1a and alcohol intake >=50 g/day. Determination of HCV antibody and liver biopsy were performed an average of 12.5 and 14 years after presumed date of contamination, respectively. CONCLUSIONS: These data provide a clearer view of the impact of this condition in this area and could help to define a comprehensive policy for patient management.


Assuntos
Biópsia por Agulha , Hepatite C Crônica/patologia , Fígado/patologia , Sistema de Registros , Adulto , Feminino , França , Genótipo , Hepacivirus/genética , Anticorpos Anti-Hepatite C/sangue , Hepatite C Crônica/etiologia , Hepatite C Crônica/virologia , Humanos , Cirrose Hepática/patologia , Cirrose Hepática/virologia , Masculino , Abuso de Substâncias por Via Intravenosa , Reação Transfusional
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