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1.
World J Gastroenterol ; 29(3): 561-578, 2023 Jan 21.
Artículo en Inglés | MEDLINE | ID: mdl-36688020

RESUMEN

BACKGROUND: Angiosarcoma is a highly malignant soft-tissue sarcoma derived from vascular endothelial cells that mainly occurs in the skin and subcutaneous tissues. Small-intestinal angiosarcomas are rare, and the prognosis is poor. CASE SUMMARY: We reported a case of primary multifocal ileal angiosarcoma and analyze previously reported cases to improve our understanding of small intestinal angiosarcoma. Small intestinal angiosarcoma is more common in elderly and male patients. Gastrointestinal bleeding, anemia, abdominal pain, weakness, and weight loss were the common symptoms. CD31, CD34, factor VIII-related antigen, ETS-related gene, friend leukemia integration 1, and von Willebrand factor are valuable immunohistochemical markers for the diagnosis of small-intestinal angiosarcoma. Small-intestinal angiosarcoma most commonly occurs in the jejunum, followed by the ileum and duodenum. Radiation and toxicant exposure are risk factors for angiosarcoma. After a definite diagnosis, the mean and median survival time was 8 mo and 3 mo, respectively. Kaplan-Meier survival analysis showed that age, infiltration depth, chemotherapy, and the number of small intestinal segments invaded by tumor lesions were prognostic factors for small intestinal angiosarcoma. Multivariate Cox regression analysis showed that chemotherapy and surgery significantly improved patient prognosis. CONCLUSION: Angiosarcoma should be considered for unexplained melena and abdominal pain, especially in older men and patients with a history of radiation exposure. Prompt treatment, including surgery and adjuvant chemotherapy, is essential to prolonging patient survival.


Asunto(s)
Hemangiosarcoma , Neoplasias del Yeyuno , Humanos , Masculino , Anciano , Hemangiosarcoma/diagnóstico , Hemangiosarcoma/terapia , Hemangiosarcoma/patología , Células Endoteliales/patología , Intestino Delgado/patología , Neoplasias del Yeyuno/diagnóstico , Neoplasias del Yeyuno/terapia , Neoplasias del Yeyuno/patología , Pronóstico , Factor de von Willebrand
2.
Artículo en Chino | MEDLINE | ID: mdl-23002555

RESUMEN

OBJECTIVE: In order to understand the production mechanism of interferon and provide a scientific basis for preventionand clinical therapy, the expression changes of Toll-like receptor (TLR3) mRNA and the role of TLR3 in human lung epithelial cells (A549 cells) infected with respiratory syncytial virus (RSV) were investigated in this study. METHODS: RSV infected A549 cells were treated with or without specific antibodies of TLR3 and collected at the selected timepoints after RSV infection (4, 8, 12, 16 and 24h). The expressions of TLR3, IFN-alpha, IFN-beta and RSV F mRNA were evaluated by RT-PCR. RESULT: It was found that RSV infection could markedly up-regulate the mRNA expression of TLR3, IFN-alpha, IFN-beta and RSV F protein in a time-dependent manner as the 24h mRNA expressions of them were 4 times, 3 times, 3 times and 0.7 times more than the basic expression, respectively. Treatment of TLR3 specific antibodies, whereas, significantly down-regulated the activation of TLR3. The mRNA expression of IFN-alpha and IFN-1beta also decreased accordingly and that of IFN-beta reduced more obviously than IFN-alpha, but that of RSV F protein rose significantly. CONCLUSION: Above data indicate that RSV infection could induce an apparent increase of antiviral genes of IFN-alpha and IFN-beta by activating TLR3 in human lung epithelial cells and the activated cells mediated Type I interferon is antiviral, which suggesting that TLR3 might play an important role in antiviral activity of RSV-infected human lung epithelial cells.


Asunto(s)
Células Epiteliales/inmunología , Pulmón/inmunología , Virus Sincitiales Respiratorios/inmunología , Receptor Toll-Like 3/fisiología , Células Epiteliales/virología , Humanos , Interferón-alfa/genética , Interferón beta/genética , Pulmón/virología , ARN Mensajero/análisis , Factores de Tiempo , Receptor Toll-Like 3/genética , Proteínas Virales de Fusión/genética
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