Peripheral T cell lymphocytosis is a rare finding in association with malig
nant thymomas. In the majority of previous cases, the tumours have behaved
aggressively with symptoms arising from local invasion. We describe a patie
nt with ocular myasthenia gravis who presented with a rapidly progressive p
olymyositis and neuropathy and who was subsequently found to have a thymic
mass and a mild T cell lymphocytosis. The thymoma did not give rise to loca
l symptoms and showed no evidence of progression over a 14-month period of
follow-up. The possibility of an underlying thymic tumour should be conside
red in any patient with chronic T cell lymphocytosis if the circulating cel
ls show mature morphology and there is no molecular evidence of monoclonali
ty.