Noncirrhotic portal hypertension in primary biliary cholangitis with coexisting CREST syndrome

Primary Biliary Cholangitis (PBC) is an autoimmune liver disease that is sometimes associated with CREST (calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) syndrome. If left untreated, PBC eventually progresses to liver cirrhosis. We describe an adult...

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Veröffentlicht in:Clinics and research in hepatology and gastroenterology 2023-05, Vol.47 (5), p.102114, Article 102114
Hauptverfasser: Malkani, Kabir V., Jesudian, Arun B., Luo, Jean J., Schonfeld, Emily A.
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Sprache:eng
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Zusammenfassung:Primary Biliary Cholangitis (PBC) is an autoimmune liver disease that is sometimes associated with CREST (calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) syndrome. If left untreated, PBC eventually progresses to liver cirrhosis. We describe an adult patient with CREST-PBC who presented with recurrent variceal bleeding and ultimately required transjugular intrahepatic portosystemic shunt (TIPS) insertion. Liver biopsy excluded cirrhosis, resulting in a diagnosis of noncirrhotic portal hypertension. This case report describes the pathophysiology of presinusoidal portal hypertension as a rare complication of PBC and its association with coexisiting CREST.
ISSN:2210-7401
2210-741X
DOI:10.1016/j.clinre.2023.102114