
Rare case of acute on chronic hepatic failure in a patient with multiple myeloma-associated amyloidosis
Author(s) -
Muzammil Khan,
Mamoon Ur Rashid,
Waqas Ullah,
Ishtiaq Hussain,
Abu Hurairah
Publication year - 2020
Publication title -
bmj case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.231
H-Index - 26
ISSN - 1757-790X
DOI - 10.1136/bcr-2019-231563
Subject(s) - medicine , multiple myeloma , amyloidosis , pathology , malignancy , al amyloidosis , rare disease , biopsy , disease , immunoglobulin light chain , immunology , antibody
Amyloidosis is the extracellular deposition of unique protein fibrils in different tissue organs. It is most commonly associated with B-cell malignancy such as multiple myeloma or Waldenstrom macroglobulinaemia. It involves the liver, heart, kidney, peripheral nerves and soft tissues. Liver however is affected, but clinically apparent disease is very rare. Hepatomegaly and mild elevation of alkaline phosphatase is the most common presentation in patients with liver involvement. Acute hepatic failure is a rare presentation with myeloma-induced amyloidosis. The diagnosis can be difficult requiring biopsy or sometimes special staining of the tissue. Management is still very challenging.