Sarcoidosis and common variable immune deficiency can rarely present simult
aneously in the same individual. We describe a child who presented with bot
h disorders. The diagnosis of sarcoidosis was delayed because of the atypic
al appearances of the liver biopsy. She failed to respond to intravenous im
munoglobulin but improved once cyclosporin and corticosteroids were added t
o her treatment regimen. It is important that the co-existence of both diso
rders is recognised so that treatment with a combination of intravenous imm
unoglobulin and immunosuppression can be in instituted to treat both the im
mune deficiency as well as the granulomatous disorder. As illustrated here,
patients may fail to respond if either modality is used alone.