Current therapies and clinical controversies in the management of primary sclerosing cholangitis-Reference-Cited by-同舟云学术

Current therapies and clinical controversies in the management of primary sclerosing cholangitis

Published:2000-04 Issue:2 Volume:2 Page:99-103
ISSN:1522-8037
Container-title:Current Gastroenterology Reports
language:en
Short-container-title:Curr Gastroenterol Rep

Author:

Prall Richard T.,Lindor Keith D.,Wiesner Russell H.,LaRusso Nicholas F.

Publisher

Springer Science and Business Media LLC

Subject

Gastroenterology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11894-000-0092-y.pdf

Reference35 articles.

1. Ernst O, Asselah T, Sergent G, et al.: MR cholangiography in primary sclerosing cholangitis. Am J Roentgenol 1998, 171:1027–1030.

2. Keiding S, Hansen SB, Rasmussen HH, et al.: Detection of cholangiocarcinoma in primary sclerosing cholangitis by positron emission tomography [see comments]. Hepatology 1998, 28:700–706. This report describes the successful use of positron emission tomography scanning to detect cholangiocarcinomas in patients with PSC. The advantage to this technique seems to be a greater sensitivity for finding small tumors, some as small as one centimeter, when presumably intervention would be the most effective. Prospective studies should be done to confirm this.

3. Kim W, Lindor K, Broome U, et al.: Independent validation of the Mayo natural history model for primary sclerosing cholangitis [abstract]. Hepatology 1999, 30:A1266.

4. Shetty K, Rybicki L, Carey WD: The Child-Pugh classification as a prognostic indicator for survival in primary sclerosing cholangitis. Hepatology 1997, 25:1049–1053.

5. Kim WR, Poterucha JJ, Wiesner RH, et al.: The relative role of the Child-Pugh classification and the Mayo natural history model in the assessment of survival in patients with primary sclerosing cholangitis. Hepatology 1999, 29:1643–1648. This paper reviews the most accurate prognostic method to date which remains clinically useful.

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