The clinical and pathological features of four liver biopsies and 12 a
utopsies from 1981-1990 with hepatic amyloidosis were reviewed. All of
the patients had a history of both intravenous and subcutaneous cocai
ne and heroin use with chronic suppurative skin ulcers. Five patients
were proven to have the acquired immunodeficiency syndrome at autopsy.
Systemic amyloidosis was diagnosed in only five out of the 16 patient
s prior to death. Hepatomegaly was present in 12 patients. The amyloid
protein was AA in 14 and AL in one case. Definitive characterization
of the amyloid substance was not possible in one case. There was no ev
idence of multiple myeloma or a plasma cell dyscrasia in the one patie
nt with AL amyloid. The amyloid distribution in the liver was both par
enchymal and vascular in 12 cases. Cholestasis, which appeared to occu
r preterminally, was the only histological finding that correlated wit
h the patient's clinical condition. The histological pattern of amyloi
d in the liver could not predict the type of amyloid protein that was
identified. Amyloidosis should be considered in the differential diagn
osis of unexplained hepatomegaly in the acquired immunodeficiency synd
rome with chronic suppurative infections.