Abstract
Early-onset benign childhood occipital seizure susceptibility syndrome (EBOSS) recently
described by Panayiotopoulos, is an early-onset variant of benign childhood epilepsy
with occipital paroxysms. EBOSS is characterized by partial seizures that are predominantly
manifested at night and associated with deviation of the eyes, vomiting and impairment
of consciousness, but without ictal visual symptoms or postictal headache. The clinical
features of our case were consistent with those of EBOSS, and we therefore diagnosed
the patient as having a typical form of EBOSS. Neuroimaging by CT, MRI and MR angiography
did not reveal a focal lesion. Interictal single photon emission computed tomography
(SPECT) revealed decreased cerebral blood flow in the right occipital region corresponding
to the epileptogenic focus shown on EEG. It remains unclear whether our finding on
SPECT reflects secondary hypoperfusion due to minor morphological abnormality or immediate
functional hypoperfusion. No reference to SPECT in a case of EBOSS has appeared in
the literature to date. This report provides a better understanding of benign childhood
epileptic syndromes with occipital spikes.
Keywords
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Article info
Publication history
Accepted:
July 30,
2001
Received in revised form:
July 28,
2001
Received:
March 15,
2001
Identification
Copyright
© 2001 Elsevier Science B.V. Published by Elsevier Inc. All rights reserved.