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Primary Hepatic Amyloidosis Presenting as Acute-on-Chronic Liver Failure.
Premkumar, Madhumita; Rangegowda, Devaraja; Vyas, Tanmay; Kulkarni, Anand; Grover, Shrruti; Mahiwall, Rakhi; Sarin, Shiv Kumar.
Afiliación
  • Premkumar M; Department of Hepatology, Institute of Liver and Biliary Sciences, Vasant Kunj, New Delhi, India.
  • Rangegowda D; Department of Hepatology, Institute of Liver and Biliary Sciences, Vasant Kunj, New Delhi, India.
  • Vyas T; Department of Hepatology, Institute of Liver and Biliary Sciences, Vasant Kunj, New Delhi, India.
  • Kulkarni A; Department of Hepatology, Institute of Liver and Biliary Sciences, Vasant Kunj, New Delhi, India.
  • Grover S; Department of Pathology, Institute of Liver and Biliary Sciences, Vasant Kunj, New Delhi, India.
  • Mahiwall R; Department of Hepatology, Institute of Liver and Biliary Sciences, Vasant Kunj, New Delhi, India.
  • Sarin SK; Department of Hepatology, Institute of Liver and Biliary Sciences, Vasant Kunj, New Delhi, India.
ACG Case Rep J ; 4: e22, 2017.
Article en En | MEDLINE | ID: mdl-28286788
ABSTRACT
Systemic amyloidosis of amyloid light chain associated protein (AL), also called primary amyloidosis, frequently involves the liver, but rarely causes clinically apparent liver disease. The more common presentation is with acute renal failure. Hepatomegaly and mild elevation of alkaline phosphatase are the most common clinical and biochemical findings, respectively. We report a case of systemic amyloidosis of AL that clinically presented as acute-on-chronic liver failure and resulted in a fatal clinical course in a 56-year-old man.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ACG Case Rep J Año: 2017 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ACG Case Rep J Año: 2017 Tipo del documento: Article País de afiliación: India