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1.
The Korean Journal of Gastroenterology ; : 359-362, 2017.
Artigo em Inglês | WPRIM | ID: wpr-165095

RESUMO

In patients with inflammatory bowel disease (IBD), cytomegalovirus (CMV) infections could aggravate the course of IBD but it is difficult to distinguish CMV infection from IBD exacerbation endoscopically. Usually, CMV tends to localize to the colon and other organic involvements were reported very rare in the IBD patients. Herein, we report a case that CMV gastric ulcer complicated with pyloric obstruction in a patient with ulcerative colitis during ganciclovir therapy, which was resolved by surgical gastrojejunostomy with review of literature.


Assuntos
Humanos , Colite Ulcerativa , Colo , Citomegalovirus , Ganciclovir , Derivação Gástrica , Obstrução da Saída Gástrica , Doenças Inflamatórias Intestinais , Úlcera Gástrica , Úlcera
2.
Journal of Korean Medical Science ; : 65-69, 2005.
Artigo em Inglês | WPRIM | ID: wpr-110320

RESUMO

Mannose-binding lectin (MBL) plays an important role in immune defense. This study was undertaken to investigate the association between hepatitis B virus infection and polymorphisms of MBL gene. We assessed the single nucleotide polymorphism at codon 54 in exon 1 of MBL in patients with hepatitis B virus infection and HBsAg negative controls in Korean population. A total of 498 enrolled subjects was classified into four groups. Group 1; Clearance, Group 2; Inactive healthy carrier, Group 3; Chronic hepatitis, Group 4; Liver cirrhosis. MBL gene polymorphisms at codon 54 led to three genotypes (G/G, G/A, A/A). When we divided subjects into clearance group (group 1) and persistence group (group 2-4), G/G genotype and A-allele carrier were observed in 55.6% and 44.4% in clearance group, 64.8% and 35.2% in persistence group (p=0.081), respectively. When hepatitis B virus persistent cases were divided into inactive healthy carrier (group 2) and disease progression group (group 3 and 4), MBL gene polymorphisms at codon 54 were not related to disease progression (p=0.166). MBL gene polymorphism at codon 54 was not associated with the clearance of hepatitis B virus infection nor progression of disease in chronic hepatitis B virus infection.


Assuntos
Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Alelos , Códon , Progressão da Doença , Fibrose , Genótipo , Hepatite , Hepatite B/genética , Vírus da Hepatite B/metabolismo , Heterozigoto , Coreia (Geográfico) , Lectinas , Lectina de Ligação a Manose/química , Polimorfismo Genético , Polimorfismo de Nucleotídeo Único
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