Literature DB >> 6661105

[Hereditary hemorrhagic telangiectasia. Report of a case].

J A Kouyoumdjian, A R Gagliardi.   

Abstract

A case of hereditary hemorrhagic teleangiectasia (HHT) or Rendu-Osler-Weber disease with neurological involvement is reported. The patient presented a diffuse cortical dysfunction with seizures after a gastric haemorrhage disturbance. The authors could not find vascular malformations of brain or pulmonary arteriovenous fistula (PAVF), so a anoxic encephalopathy followed a shock or a microangiopathic dysfunction is postulated. The main neurological manifestations of HHT are discussed, emphasizing in the first place the role of the PAVF on the genesis of cerebral hypoxemia and brain abscess and occasionally a cerebral thrombosis caused by polycythemia and in the second place the vascular malformations of brain and spinal cord. The portal-systemic encephalopathy may also occur as a neurological complication in few cases.

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Year:  1983        PMID: 6661105     DOI: 10.1590/s0004-282x1983000400011

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  1 in total

Review 1.  Giant spinal perimedullary fistula in hereditary haemorrhagic telangiectasia: diagnosis, endovascular treatment and review of the literature.

Authors:  F Mont'Alverne; M Musacchio; V Tolentino; F Belzile; C Riquelme; A Tournade
Journal:  Neuroradiology       Date:  2003-10-14       Impact factor: 2.804

  1 in total

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