Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
CASE REPORTS
Immunoglobulin Light Chain Amyloidosis with Severe Liver Dysfunction Accompanied by Factor X Deficiency
Yong-mei GuoNagi TakahashiKen MiyabeMakoto YoshidaFumito AbeTakaya YamashitaMiho NaraTomoko YoshiokaKenichi OhashiAkiteru GotoNaoto Takahashi
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JOURNAL OPEN ACCESS

2019 Volume 58 Issue 20 Pages 3039-3043

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Abstract

Severe hepatic failure is rarely a cause of death in patients with immunoglobulin light chain (AL) amyloidosis. We herein report a case of AL amyloidosis involving a bleeding tendency due to factor X deficiency and marked hepatic involvement of amyloidosis. The patient died due to severe liver dysfunction two weeks after admission. The diagnosis was confirmed histologically by AL-λ amyloidosis, with the liver and spleen as the main lesions, on an autopsy. As treatment-related toxicity is strong in advanced cases, appropriate treatments are required to improve the prognosis of AL amyloidosis with severe liver dysfunction.

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© 2019 by The Japanese Society of Internal Medicine
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