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1.
BMC Gastroenterol ; 12: 101, 2012 Aug 06.
Artículo en Inglés | MEDLINE | ID: mdl-22866875

RESUMEN

BACKGROUND: A retrospective study was performed to assess the causes, diagnostic methods for, and clinical features of, jejunoileal hemorrhage in Shandong province, China and to derive recommendations for management of this condition from these data. METHODS: We performed a retrospective systematic collection of data from between January 1999 and December 2008 in seven cities in Shandong province, China, identified 72 patients with jejunoileal hemorrhage and analyzed the relevant clinical data. RESULTS: Overall, tumors were the most common cause of jejunoileal hemorrhage (42 patients, 58.3%). The causes of this condition were significantly different (P < 0.05) in male and female patients. In male patients, the commonest factors were tumor (52.2%), enteritis (17.4%) and angiopathy (15.2%). However, in female patients, tumors accounted for a greater proportion of cases (18/26, 69.2%). In 38 cases (52.8%) the diagnosis was made by intraoperative enteroscopy or laparotomy, in 14 by capsule endoscopy and in the remainder by radiological methods. The most frequent presentation was melena (62.7%), followed by maroon stools (26.9%) and hematochezia (9.0%). Of the 72 patients,laparotomy is the main treatment method. CONCLUSION: Tumor, enteritis and angiopathy and diverticular disease are the most common causes of jejunoileal hemorrhage in Shandong province, China. The main clinical manifestations are bloody stools, most commonly in the form of melena, with or without abdominal pain. We recommend that female patients over the age of 40 with jejunoileal hemorrhage accompanied by abdominal pain should undergo urgent further assessment because of the strong probability of jejunoileal tumor.


Asunto(s)
Hemorragia Gastrointestinal/diagnóstico , Enfermedades del Íleon/diagnóstico , Enfermedades del Yeyuno/diagnóstico , Dolor Abdominal/diagnóstico , Dolor Abdominal/diagnóstico por imagen , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , China , Divertículo/complicaciones , Divertículo/diagnóstico , Divertículo/diagnóstico por imagen , Endoscopía/métodos , Enteritis/complicaciones , Enteritis/diagnóstico , Enteritis/diagnóstico por imagen , Femenino , Hemorragia Gastrointestinal/diagnóstico por imagen , Hemorragia Gastrointestinal/etiología , Humanos , Enfermedades del Íleon/complicaciones , Enfermedades del Íleon/diagnóstico por imagen , Enfermedades del Yeyuno/complicaciones , Enfermedades del Yeyuno/diagnóstico por imagen , Masculino , Melena/diagnóstico , Melena/diagnóstico por imagen , Persona de Mediana Edad , Neoplasias/complicaciones , Neoplasias/diagnóstico , Neoplasias/diagnóstico por imagen , Enfermedades Vasculares Periféricas/complicaciones , Enfermedades Vasculares Periféricas/diagnóstico , Enfermedades Vasculares Periféricas/diagnóstico por imagen , Radiografía , Estudios Retrospectivos , Adulto Joven
2.
Kaohsiung J Med Sci ; 34(9): 479-486, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-30173777

RESUMEN

MicroRNAs are important regulators during human growth and development. Emerging evidence indicates that microRNAs play important roles in colorectal cancer. The aim of this study is to reveal the biological function and direct target gene of miR-483 in colorectal cancer. The biological function of miR-483 on the proliferation and migration of colon cancer cells was then examined by Edu assay and transwell assay, respectively. Our findings revealed that miR-483 mimic could significantly inhibit cell proliferation and migration. The target gene of miR-483 was predicted by target scan software and identified by a dual fluorescence reporter system which showed that TRAF1 was a direct target gene of miR-483 in SW480 cell line. These data suggest that miR-483 is a colorectal cancer suppressor which could inhibit cell proliferation and migration, possibly via targeting TRAF1. The miR-483 could be a potential treatment target for colorectal cancer.


Asunto(s)
Neoplasias del Colon/metabolismo , MicroARNs/metabolismo , Factor 1 Asociado a Receptor de TNF/metabolismo , Línea Celular Tumoral , Movimiento Celular/genética , Movimiento Celular/fisiología , Proliferación Celular/genética , Proliferación Celular/fisiología , Neoplasias del Colon/genética , Regulación Neoplásica de la Expresión Génica/genética , Humanos , MicroARNs/antagonistas & inhibidores , MicroARNs/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Factor 1 Asociado a Receptor de TNF/genética
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