Clinically apparent involvement of the heart and nervous system occurs
in a relatively small number of patients with sarcoidosis. The diagno
sis of myocardial and neurological sarcoidosis is difficult because an
atomic presence of granulomas without clinical dysfunction is an impor
tant feature of sarcoidosis. The chest radiography is abnormal in 8 of
every 10 patients with myocardial or neurosarcoidosis. Serum angioten
sin-converting enzyme and gallium uptake studies may provide some indi
cation of the extent and severity of the granulomatous process. Cortic
osteriods are the mainstay of therapy but chloroquine or hydroxychlori
quine, methotrexate, and azathioprine are also effective. Prognosis of
myocardial and neurological sarcoidosis is poor.