2017, Number 6
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Ann Hepatol 2017; 16 (6)
Endoscopic Management of Primary Sclerosing Cholangitis
Barkin JA, Levy C, Souto EO
Language: English
References: 72
Page: 842-850
PDF size: 258.09 Kb.
ABSTRACT
Primary sclerosing cholangitis (PSC) remains a rare but potentially devastating chronic, cholestatic liver disease. PSC causes
obstruction of intra- and/or extra-hepatic bile ducts by inflammation and fibrosis, leading to biliary obstruction, cirrhosis and portal
hypertension with all associated sequelae. The most dreaded consequence of PSC is cholangiocarcinoma, occurring in 10-20% of
patients with PSC, and with population-based estimates of a 398-fold increased risk of cholangiocarcinoma in patients with PSC
compared to the general population. We use the 4-D approach to endoscopic evaluation and management of PSC based on currently
available evidence. After laboratory testing with liver chemistries and high-quality cross-sectional imaging with MRCP, the first D is
Dominant stricture diagnosis and evaluation. Second, Dilation of strictures found during ERCP is performed using balloon dilation to
as many segments as possible. Third, Dysplasia and cholangiocarcinoma diagnosis is performed by separated brushings for conventional
cytology and fluorescence in situ hybridization (FISH), and consideration for direct cholangioscopy with SpyGlass
™. Fourth
and finally, Dosing of antibiotics is critical to prevent peri-procedural cholangitis. The aim of this review article is to explore endoscopic
tools and techniques for the diagnosis and management of PSC and provide a practical approach for clinicians.
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