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Retinal vein thrombosis associated with pegylated-interferon and ribavirin combination therapy for chronic hepatitis C
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作者 iman zandieh Mohamed Adenwalla +2 位作者 Cindy Cheong-Lee Patrick E Ma Eric M Yoshida 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第30期4908-4910,共3页
An estimated 300 million people worldwide suffer from chronic hepatitis C with a prevalence of 0.8%-1.0% of the general population in Canada. An increasing pool of evidence exists supporting the use of pegylated-inter... An estimated 300 million people worldwide suffer from chronic hepatitis C with a prevalence of 0.8%-1.0% of the general population in Canada. An increasing pool of evidence exists supporting the use of pegylated-interferon (pegIFN) and ribavirin combination therapy for hepatitis C. We report a 49-year old male of North American aboriginal descent with chronic hepatitis C (genotype 2b). Biopsy confirmed that he had cirrhosis with a 2-wk history of left eye pain and decreased visual acuity. He developed retinal vein thrombosis after 16 of 24 wk of pegIFN-α 2a and ribavirin combination therapy. He was urgently referred to a retinal specialist and diagnosed with non-ischemic central retinal vein occlusion of the left eye. PegIFN and ribavirin combination therapy was discontinued and HCV RNA was undetectable after 16 wk of treatment. Hematologic investigations revealed that the patient was a factor V Leiden heterozygote with mildly decreased protein C activity. Our patient had a number of hypercoagulable risk factors, including factor V Leiden heterozygosity, cirrhosis, and hepatitis C that alone would have most likely remained clinically silent. We speculate that in the setting of pegIFN treatment, these risk factors may coalesce and cause the retinal vein thrombosis. 展开更多
关键词 INTERFERON PEGYLATED-INTERFERON Hepatitis C CIRRHOSIS Retinal vein thrombosis THROMBOSIS Central retinal vein occlusion
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A potpourri of pancreatic issues
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作者 iman zandieh Michael F Byrne 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第47期6327-6332,共6页
Autoimmune pancreatitis has emerged over the last 40 years from a proposed concept to a well established and recognized entity. As an efficient mimicker of pancreatic carcinoma, its early and appropriate recognition a... Autoimmune pancreatitis has emerged over the last 40 years from a proposed concept to a well established and recognized entity. As an efficient mimicker of pancreatic carcinoma, its early and appropriate recognition are crucial. With mounting understanding of its pathogenesis and natural history, significant advances have been made in the diagnosis of autoimmune pancreatitis. The characteristic laboratory features and imaging seen in autoimmune pancreatitis are reviewed along with some of the proposed diagnostic criteria and treatment algorithms. 展开更多
关键词 Autoimmune pancreatitis Chronic pancreatitis Idiopathic pancreatitis Sclerosing pancreatitis
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