Splenic Arteriovenous Malformation Manifestated by Thrombocytopenia in Hereditary Hemorrhagic Telangiectasia: A Case Report
Journal of the Korean Radiological Society
; : 197-200, 2008.
Article
в Ko
| WPRIM
| ID: wpr-32180
Ответственная библиотека:
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.
Key words
Полный текст:
1
База данных:
WPRIM
Основная тема:
Arteriovenous Malformations
/
Spleen
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Telangiectasia, Hereditary Hemorrhagic
/
Telangiectasis
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Thrombocytopenia
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Epistaxis
/
Gastrointestinal Tract
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Cerebrum
/
Liver
/
Lung
Язык:
Ko
Журнал:
Journal of the Korean Radiological Society
Год:
2008
Тип:
Article