ABSTRACT
Sarcoidosis is a multisystem granulomatous disease of unknown cause (1).
It commonly affects young and middle-aged adults. The diagnosis can be easily made in the cases of typical clinical manifestations such as bilateral
hilar adenopathy (BHL) and erythema nodosum. However, sarcoidosis is
fundamentally a chronic disease and clinically tends to show a regression
and relapse and variable signs and symptoms, as well. It is difficult to diag-
nose organ involvement systemically if the physician does not pay attention
to the possibility of sarcoidosis, especially when clinical features are not
typical and are nonspecific. Neurological involvement in sarcoidosis is a
typical example with a diagnostic challenge.
