Surgery in severe factor XIII deficiency: report of a case of epilepsy neurosurgery and review

Factor XIII (FXIII) deficiency is a rare autosomal recessive congenital disorder of haemostasis, associated with a high risk of intracranial haemorrhage. Intracranial haemorrhage can result in neurological sequelae including seizure disorders. In some cases, medically intractable epilepsy led to epi...

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Veröffentlicht in:Haemophilia : the official journal of the World Federation of Hemophilia 2003-01, Vol.9 (1), p.121-124
Hauptverfasser: Pernod, G., Barro, C., Arnutti, B., Blanc-Jouvan, F., Garrel, S., Kahn, P., Minotti, L., Koudsie, A., Benabid, A. L., Wrobleski, I., Joannard, A., Polack, B.
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Sprache:eng
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Zusammenfassung:Factor XIII (FXIII) deficiency is a rare autosomal recessive congenital disorder of haemostasis, associated with a high risk of intracranial haemorrhage. Intracranial haemorrhage can result in neurological sequelae including seizure disorders. In some cases, medically intractable epilepsy led to epilepsy surgery. Little has been reported on the management of FXIII deficiency during surgery, and there is only a few data on the management, safety and efficacy of epilepsy surgery in the patients with haemostatic disorder. We report here an epilepsy neurosurgery in a case of severe FXIII deficiency.
ISSN:1351-8216
1365-2516
DOI:10.1046/j.1365-2516.2003.00700.x