Year 2020 / Volume 112 / Number 10
Letter
Liver failure caused by Kappa-light chain amyloidosis: a rare case report of multiple myeloma

814-815

DOI: 10.17235/reed.2020.6823/2019

Carles Suria Bolufer, Inmaculada Ortiz Polo, Joana Carolina Gómez Adrián,

Abstract
Liver failure (LF) is a severe entity, which represents a diagnostic challenge for clinicians. Knowing the etiology of liver aggression is key for its management. We present a rare case of cholestatic LF secondary to primary AL (kappa-light chain) amyloidosis as a presentation associated to multiple myeloma.
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References
1. Madan S, Dispenzieri A, Lacy MQ, et al. Clinical features and treatment response of light chain (AL) amyloidosis diagnosed in patients with previous diagnosis of multiple myeloma. Mayo Clin Proc. 2010;85(3):232.
2. Park MA, Mueller PS, Kyle RA, et al. Primary (AL) hepatic amyloidosis: clinical features and natural history in 98 patients. Medicine (Baltimore). 2003;82(5):291.
3. Alireza Sadeghi, Maliheh Nejati, Azadeh Moghaddas. A Rare Presentation of Multiple Myeloma: A Case Report of Hepatic Amyloidosis. Iran J Med Sci. 2019; 44(4): 342–346.
4. Gertz MA. Immunoglobulin light chain amyloidosis: 2018 Update on diagnosis, prognosis, and treatment. Am J Hematol. 2018; 93(9): 1169-1180.
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Suria Bolufer C, Ortiz Polo I, Gómez Adrián J. Liver failure caused by Kappa-light chain amyloidosis: a rare case report of multiple myeloma. 6823/2019


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Publication history

Received: 16/12/2019

Accepted: 17/01/2020

Online First: 21/09/2020

Published: 07/10/2020

Article revision time: 27 days

Article Online First time: 280 days

Article editing time: 296 days


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