| Literature DB >> 23382642 |
Ileana Duca1, Patricia Ramírez de la Piscina, Silvia Estrada, Rosario Calderón, Katerina Spicakova, Leire Urtasun, Carlos Marra-López, Salvador Zabaleta, Raquel Bengoa, María Asunción Marcaide, Francisco García-Campos.
Abstract
Primary sclerosing cholangitis is an infrequent extraintestinal manifestation of ulcerative colitis. Damage to bile ducts is irreversible and medical therapies to prevent progression of the disease are usually ineffective. We describe a patient with long-standing ulcerative colitis, which was refractory to corticosteroid therapy who developed primary sclerosing cholangitis (biochemical stage II/IV) in the course of his pancolitis. Treatment with infliximab (5 mg/kg as an induction dose followed by maintenance doses every two months) was indicated because of steroid-dependent disease associated to primary sclerosing cholangitis as well as sacroiliitis and uveitis and previous episode of severe azathioprine-related hepatic toxicity. At present, after two years of follow-up, the patient is asymptomatic with normal liver tests and complete resumption of daily life activities. This case draws attention to the usefulness of anti-tumor necrosis factor-alpha therapy for the management of primary sclerosing cholangitis as extraintestinal manifestation of inflammatory bowel disease.Entities:
Keywords: Bile duct diseases; Infliximab; Monoclonal antibodies; Sclerosing cholangitis; Tumor necrosis factor-alpha; Ulcerative colitis
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Year: 2013 PMID: 23382642 PMCID: PMC3558587 DOI: 10.3748/wjg.v19.i4.590
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742