Clinical Neurology and Neurosurgery
Volume 109, Issue 10 , Pages 914-917, December 2007

Decompressive hemicraniectomy in a space-occupying presentation of hemiconvulsion–hemiplegia–epilepsy syndrome

  • Moncef Berhouma

      Affiliations

    • Department of Neurosurgery, National Institute of Neurology, Rue Jebbari 1007 La Rabta, Tunis, Tunisia
    • Corresponding Author InformationCorresponding author. Tel.: +216 98349177; fax: +216 71712652.
  • ,
  • Ridha Chekili

      Affiliations

    • Department of Neurosurgery, National Institute of Neurology, Rue Jebbari 1007 La Rabta, Tunis, Tunisia
  • ,
  • Ines Brini

      Affiliations

    • Department of Paediatrics, Children's Hospital, Tunis, Tunisia
  • ,
  • Nidhameddine Kchir

      Affiliations

    • Department of Pathology, La Rabta Hospital, Tunis, Tunisia
  • ,
  • Hafedh Jemel

      Affiliations

    • Department of Neurosurgery, National Institute of Neurology, Rue Jebbari 1007 La Rabta, Tunis, Tunisia
  • ,
  • Souad Bousnina

      Affiliations

    • Department of Paediatrics, Children's Hospital, Tunis, Tunisia
  • ,
  • Moncef Khaldi

      Affiliations

    • Department of Neurosurgery, National Institute of Neurology, Rue Jebbari 1007 La Rabta, Tunis, Tunisia

Received 21 June 2007; received in revised form 27 July 2007; accepted 30 July 2007.

Abstract 

A case of an acute life-threatening presentation of hemiconvulsion–hemiplegia–epilepsy (HHE) syndrome requiring an urgent decompressive hemicraniectomy is described. A 9 month-old baby had a status epilepticus following a sustained fever, leading to a comatose state and a right pupillary dilatation associated with a left hemiplegia. The MRI showed a swelling right hemisphere with marked temporal herniation. The baby underwent a decompressive right hemicraniectomy with temporal cortical biopsies. The post-operative course was favourable. The histological findings were unspecific, showing a gliotic spongiosis with disseminated granular cells. The post-operative MRI depicted a right hemisphere atrophy. To our knowledge, a space-occupying presentation of HHE syndrome requiring surgical decompression has never been described before while only a few reports dealt with the neuropathological aspects of this syndrome.

Keywords: Decompressive hemicraniectomy, Hemiconvulsion–hemiplegia–epilepsy syndrome, MRI, Neuropathology, Status epilepticus

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PII: S0303-8467(07)00208-9

doi:10.1016/j.clineuro.2007.07.027

Clinical Neurology and Neurosurgery
Volume 109, Issue 10 , Pages 914-917, December 2007