Splenic Arteriovenous Malformation Manifestated by Thrombocytopenia in Hereditary Hemorrhagic Telangiectasia: A Case Report
Journal of the Korean Radiological Society
; : 197-200, 2008.
Article
em Ko
| WPRIM
| ID: wpr-32180
Biblioteca responsável:
WPRO
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.
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Texto completo:
1
Índice:
WPRIM
Assunto principal:
Malformações Arteriovenosas
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Baço
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Telangiectasia Hemorrágica Hereditária
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Telangiectasia
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Trombocitopenia
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Epistaxe
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Trato Gastrointestinal
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Cérebro
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Fígado
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Pulmão
Idioma:
Ko
Revista:
Journal of the Korean Radiological Society
Ano de publicação:
2008
Tipo de documento:
Article