The ability of cholesteatoma to grow rapidly within the ear is well re
cognized. This study aimed to quantify the in vitro growth of choleste
atoma derived cells. Following removal of cholesteatoma explant cultur
es were established. Cellular outgrowths were subcultured and a colony
forming assay performed. Cells were repeatedly passaged every 14 days
until senescence was observed. In comparison with cells derived from
normal scalp skin, cholesteatoma derived cells demonstrated a lower co
lony forming efficiency in both primary and secondary subcultures, ach
ieved fewer passages and cell generations in serial culture, and achie
ved a lower total population expansion. No evidence was found to sugge
st an intrinsic loss of growth control. It is proposed that the majori
ty of cholesteatoma is composed of cells with a limited capacity for g
rowth. Explant studies suggested that these may be the progeny of more
highly proliferative cells situated at the neck of the cholesteatoma
sac.