Two well circumscribed tumors, oncocytic and non-oncocytic, were remov
ed from the non-cirrhotic liver of a 67 year old male, The large oncoc
ytic tumor (OCT), occupying the entire left lobe, was multilobulated w
ith focal coagulation necrosis and areas of hemorrhage. Light microsco
py revealed that it consisted of exclusively large, granular oxyphilic
cells with moderate nuclear atypia and occasional mitotic figures, wh
ich were trabecular and/or pseudoglandular in structure, but no lamell
ar fibrosis was seen. Characteristically, the OCT cells included numer
ous globular hyaline bodies (GHB) of various sizes which were stained
red with acid fuchsin and deep blue or magenta with phosphotungstic ac
id hematoxylin (PTAH), but negative for periodic acid Schiff (PAS), or
cein, rhodamine and Grimelius methods. Immunohistochemically, alpha-fe
toprotein (AFP), alpha-1-antitrypsin, alpha-1-antichymotrypsin, fibrin
ogen and ferritin were all negative. On ultrastructural examination, t
umor cells were mitochondria rich, including electron dense, ovoid or
polyhedral inclusions, with the delineated membrane identical with tha
t of the GHB. In contrast, the small tumor in the right lobe (Segment
7) was a solid adenoma with no oncocytic transition, Based on these fi
ndings, it was postulated that OCT consists of heterogenous proliferat
ion of mitochondria-rich hepatocytes which tend to induce lysosomal GH
B closely associated with mitochondrial abnormalities.