A Case of Severe Cholestasis due to Hepatic AL Amyloidosis
Author:
Publisher
S. Karger AG
Subject
Gastroenterology
Reference14 articles.
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2. Desport E, Bridoux F, Sirac C, Delbes S, Bender S, Fernandez B, et al.; Centre national de référence pour l’amylose AL et les autres maladies par dépôts d’immunoglobulines monoclonales. Al amyloidosis. Orphanet J Rare Dis. 2012 Aug;7(1):54.
3. Gertz MA, Comenzo R, Falk RH, Fermand JP, Hazenberg BP, Hawkins PN, et al. Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22 April 2004. Am J Hematol. 2005 Aug;79(4):319–28.
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1. Hepatic amyloidosis: a prevalence study and clinical characterization of a rare and severe disease;Revista Española de Enfermedades Digestivas;2022
2. Severe intrahepatic cholestasis as the initial manifestation of light chain amyloidosis;Gastroenterología y Hepatología;2021-01
3. Severe intrahepatic cholestasis as the initial manifestation of light chain amyloidosis;Gastroenterología y Hepatología (English Edition);2021-01
4. Along for the Ride: Intrahepatic Cholangiocarcinoma with Concomitant LECT2 Amyloidosis;Case Reports in Pathology;2020-07-17
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