Subacute encephalopathy with seizures in alcoholics (SESA syndrome) is
a rare disease entity following chronic alcohol ingestion. It is quit
e distinct from alcohol withdrawal syndromes, such as delirium, withdr
awal seizures or CNS complications of alcohol, such as Wernicke-Korsak
ow syndrome, central pontine myelinolysis or Marchiafava-Bignami disea
se, and was proposed in 1981 by Niedermeyer and coworkers. This syndro
me consists of multiple neurological deficits, such as hemiparesis or
hemianopia,and of recurrent focal and generalized seizures associated
with prominent EEG features (periodic lateralized discharges, PLEDs).
A 72-year-old Caucasian male with chronic alcoholism and an otherwise
unremarkable past medical history was admitted to our hospital because
of several secondary generalized simple partial seizures. Laboratory
investigations revealed elevated levels of gamma-glutamyl-transpeptida
se and of mean corpuscular volume. Other laboratory investigations and
the CSF examinations on three occasions revealed normal values. Crani
al computed and magnetic resonance tomography showed cerebral microang
iopathy and generalized atrophy. Despite triple anticonvulsive therapy
and an intravenous treatment with acyclovir and thiamine,the epilepti
c seizures persisted. Several EEGs revealed left parietooccipital pero
dic lateralized epileptiform discharges (PLEDs). The patient died of a
n intercurrent pulmonary infection about 3 months after the onset of s
ymptoms. The described clinical picture resembles the symptoms of SESA
syndrome.