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1.
Korean Journal of Gastrointestinal Endoscopy ; : 21-24, 2011.
Artigo em Coreano | WPRIM | ID: wpr-193607

RESUMO

Cytomegalovirus (CMV) is a potentially important pathogen in an immunocompromised host. CMV infection usually occurs in patients with severe immune deficiency, such as acquired immunodeficiency syndrome, organ transplantation, malignant disease, or immunosuppressive therapy. CMV can cause ulcerations anywhere in the GI tract ranging from the esophagus to the rectum, but the colon is the most susceptible organ in the GI tract. CMV infection rarely occurs but generally causes an asymptomatic or mildly symptomatic acute illness in immunocompetent patients. Some patients with gastrointestinal CMV disease do not require antiviral treatment such as ganciclovir and frequently recover with supportive therapy. Although in immunocompetent patients, antiviral therapy may be needed based on age, chronic illness, or treatment response. We experienced a case of CMV-induced multiple gastric ulcers with severe epigastric pain in an immunocompetent patient who fully recovered with supportive therapy including a proton pump inhibitor.


Assuntos
Humanos , Síndrome da Imunodeficiência Adquirida , Doença Crônica , Colo , Citomegalovirus , Esôfago , Ganciclovir , Trato Gastrointestinal , Hospedeiro Imunocomprometido , Transplante de Órgãos , Bombas de Próton , Reto , Úlcera Gástrica , Transplantes , Úlcera
2.
Korean Journal of Medicine ; : S106-S110, 2011.
Artigo em Coreano | WPRIM | ID: wpr-36742

RESUMO

Autoimmune hepatitis (AIH), primary sclerosing cholangitis (PSC), and primary biliary cirrhosis (PBC) are the major immune-mediated chronic liver diseases. They are characterized by circulating autoantibodies, hypergammaglobulinemia, unique clinical features, and associations with other autoimmune diseases, such as inflammatory bowel disease and autoimmune thyroiditis. Primary biliary cirrhosis is known to be associated with inflammatory bowel disease, such as ulcerative colitis. On the other hand, autoimmune hepatitis is rarely associated with ulcerative colitis. Here, we report a case diagnosed as autoimmune hepatitis combined with ulcerative colitis on the basis of histological and endoscopic findings.


Assuntos
Autoanticorpos , Doenças Autoimunes , Colangite Esclerosante , Colite Ulcerativa , Mãos , Hepatite Autoimune , Hipergamaglobulinemia , Doenças Inflamatórias Intestinais , Cirrose Hepática Biliar , Hepatopatias , Tireoidite Autoimune , Úlcera
3.
Korean Circulation Journal ; : 339-342, 2010.
Artigo em Inglês | WPRIM | ID: wpr-196627

RESUMO

LEOPARD syndrome (LS) is a rare hereditary disorder in Asian countries. This syndrome consists of multiple systemic abnormalities. In particular, characteristic cardiovascular effects in LS may include variable clinical manifestations from benign to life-threatening courses. The cardiac effects of this syndrome consist of left ventricular hypertrophy (LVH), pulmonary stenosis (PS), coronary artery dilatation and electrocardiogram(ECG) abnormalities. Since there are few LS patients who have undergone a complete cardiovascular evaluation, the nature and clinical prognosis of cardiovascular abnormalities in this syndrome remain uncertain. Also, there have been few reports on therapeutic strategies for cardiovascular abnormalities in LS. Here we describe a case of LS who presented with multiple cardiovascular problems and underwent successful surgical and medical treatment.


Assuntos
Humanos , Povo Asiático , Anormalidades Cardiovasculares , Vasos Coronários , Dilatação , Hipertrofia Ventricular Esquerda , Lentigo , Síndrome LEOPARD , Panthera , Prognóstico , Estenose da Valva Pulmonar
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