Primary sclerosing cholangitis
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How to Cite

1.
Vargas KA. Primary sclerosing cholangitis. Rev.méd.sinerg. [Internet]. 2018Sep.1 [cited 2024Nov.24];3(9):3-8. Available from: https://revistamedicasinergia.com/index.php/rms/article/view/135

Abstract

Primary sclerosing cholangitis (PSC) is a chronic liver disease characterized by a progressive course of cholestasis with inflammation and fibrosis of the intrahepatic and extrahepatic bile ducts. PSC is strongly associated (60-80%) with inflammatory bowel disease (IBD), mainly ulcerative colitis, and is often complicated by the development of cholangiocarcinoma. Most individuals  have no symptoms (44-56%), and the presence of primary sclerosing cholangitis is recognized only because of abnormally elevated blood levels of liver enzymes that often are performed along with a routine physical examination.

https://doi.org/10.31434/rms.v3i9.135

Keywords

cholangitis. gall bladder. fibrosis. extrahepatic. liver. intestine.
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References

1. Konstantinos N. Lazaridis, MD. (2016). Colangitis esclerosante primaria. The New England Journal of Medicine, 375, 1161-1170.

2. Siddharth Singh. (2013). Colangitis Esclerosante Primaria: Diagnóstico, Pronóstico y Manejo. Clinical Gastroenterology and Hepatology, 11, 898-907.

3. Nieun Seo, MD. (2016). Colangitis esclerosante: características clínico-patológicas, espectro de imágenes y enfoque sistémico para el diagnóstico diferencial. Korean Journal of Radiology, 17, 25.

4. Mark Feldman. (2016). Sleisenger y la enfermedad gastrointestinal y hepática de Fordtran. Philadelphia, PA: Saunders / Elsevier.

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