Tags

Type your tag names separated by a space and hit enter

[Spinal abscess in a patient with hereditary hemorrhagic telangiectasia].
Medicina (B Aires). 2007; 67(6 Pt 2):714-6.M

Abstract

Rendu-Osler-Weber syndrome is an autosomal dominant disorder characterized by multiple skin and mucosal telangiectasis and multiorgan arteriovenous malformations. Neurological manifestations may occur because of cerebral arteriovenous malformations, intracranial hemorrhage, and most commonly by ischemic stroke and brain abscess secondary to paradoxical embolization in patients with pulmonary arteriovenous malformations. Intramedullary abscess is a rare, unusual condition, in Rendu-Osler-Weber syndrome. We report the case of a 56 years old woman, with a familial history of Rendu-Osler-Weber syndrome, admitted to intensive care with acute quadriplegia and hypoxemia. Our diagnosis was pulmonary arteriovenous malformations and intramedullary abscess.

Authors+Show Affiliations

Servicio de Cuidados Intensivos, Hospital Británico, Buenos Aires, Argentina.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

spa

PubMed ID

18422064

Citation

Maldonado, Lorena V., et al. "[Spinal Abscess in a Patient With Hereditary Hemorrhagic Telangiectasia]." Medicina, vol. 67, no. 6 Pt 2, 2007, pp. 714-6.
Maldonado LV, Soloaga ED, Veltri MA, et al. [Spinal abscess in a patient with hereditary hemorrhagic telangiectasia]. Medicina (B Aires). 2007;67(6 Pt 2):714-6.
Maldonado, L. V., Soloaga, E. D., Veltri, M. A., Chertcoff, F. J., & Ubaldini, J. E. (2007). [Spinal abscess in a patient with hereditary hemorrhagic telangiectasia]. Medicina, 67(6 Pt 2), 714-6.
Maldonado LV, et al. [Spinal Abscess in a Patient With Hereditary Hemorrhagic Telangiectasia]. Medicina (B Aires). 2007;67(6 Pt 2):714-6. PubMed PMID: 18422064.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Spinal abscess in a patient with hereditary hemorrhagic telangiectasia]. AU - Maldonado,Lorena V, AU - Soloaga,Elías D, AU - Veltri,Miguel A, AU - Chertcoff,Felipe J, AU - Ubaldini,Jorge E, PY - 2008/4/22/pubmed PY - 2009/1/27/medline PY - 2008/4/22/entrez SP - 714 EP - 6 JF - Medicina JO - Medicina (B Aires) VL - 67 IS - 6 Pt 2 N2 - Rendu-Osler-Weber syndrome is an autosomal dominant disorder characterized by multiple skin and mucosal telangiectasis and multiorgan arteriovenous malformations. Neurological manifestations may occur because of cerebral arteriovenous malformations, intracranial hemorrhage, and most commonly by ischemic stroke and brain abscess secondary to paradoxical embolization in patients with pulmonary arteriovenous malformations. Intramedullary abscess is a rare, unusual condition, in Rendu-Osler-Weber syndrome. We report the case of a 56 years old woman, with a familial history of Rendu-Osler-Weber syndrome, admitted to intensive care with acute quadriplegia and hypoxemia. Our diagnosis was pulmonary arteriovenous malformations and intramedullary abscess. SN - 0025-7680 UR - https://www.unboundmedicine.com/medline/citation/18422064/[Spinal_abscess_in_a_patient_with_hereditary_hemorrhagic_telangiectasia]_ DB - PRIME DP - Unbound Medicine ER -