Splenic Arteriovenous Malformation Manifestated by Thrombocytopenia in Hereditary Hemorrhagic Telangiectasia: A Case Report
Journal of the Korean Radiological Society
;
: 197-200, 2008.
Artículo
en Coreano
| WPRIM
| ID: wpr-32180
ABSTRACT
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant inherited disease characterized by epistaxis, telangiectases and visceral arteriovenous malformations (AVMs). The involvement of the gastrointestinal tract, liver, lung and cerebrum for HHT has been described, whereas little is known about AVMs of the spleen. We report here the radiological findings of a case of a splenic AVM manifested by thrombocytopenia in HHT.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Malformaciones Arteriovenosas
/
Bazo
/
Telangiectasia Hemorrágica Hereditaria
/
Telangiectasia
/
Trombocitopenia
/
Epistaxis
/
Tracto Gastrointestinal
/
Cerebro
/
Hígado
/
Pulmón
Idioma:
Coreano
Revista:
Journal of the Korean Radiological Society
Año:
2008
Tipo del documento:
Artículo
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