Objectives - In juvenile myoclonic epilepsy (JME) neuroimaging procedures a
re usually unnecessary but are often performed following the first generali
zed tonic-clonic seizure before a specific diagnosis has been reached. Our
aim was to evaluate the influence of abnormal findings on the clinical pres
entation and prognosis of JME. Material and methods - We retrospectively an
alyzed all medical records of JME patients first referred in two epilepsy c
enters (Marseilles, Nice) between 1981 and 1998. Results - Among 170 consec
utive unselected newly diagnosed JME patients, neuroimaging was performed i
n 82 cases (MRI: 22, CT: 75, including MRI + CT: 15). In 4 subjects, specif
ic neurological abnormalities had justified neuroimaging: severe head traum
a after the onset of JME (2, both with lesions related to the trauma), mult
iple sclerosis with onset after JME (1, with normal MRI before the onset of
multiple sclerosis and abnormal, specific findings later), severe mental r
etardation (1, with diffuse MRT changes but a typical electro-clinical pres
entation and evolution). In the other 78 cases, 9 had abnormal findings: co
mmon arachnoid cyst (3), mild diffuse cerebral atrophy and ventricular enla
rgement (1), mild ventricular enlargement only (3), septum lucidum cavum (1
), mildly increased T-2 signal in the left temporal lobe (1). Abnormal neur
oimaging did not influence therapeutic decisions or prognosis. Conclusions
- These data confirm that neuroimaging procedures should not be routinely p
erformed in patients with typical JME, unless additional neurological probl
ems, that are unrelated to the diagnosis of epilepsy, occur.