A Case of Hereditary Hemorrhagic Telangiectasia / 대한간학회지
The Korean Journal of Hepatology
;
: 514-518, 2000.
Artigo
em Coreano
| WPRIM
| ID: wpr-209194
ABSTRACT
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant inherited disease characterized by telangiectasias of the skin, mucous membranes, and various organ system. HHT is not unusual in western countries but there were several reported cases of HHT in Korea. Recently we evaluated a 40-year-old postpartum female who had been suffering from recurrent epistaxis and peripartum dyspnea. The patient was diagnosed as a HHT complicated by high output heart failure caused by intrahepatic arteriovenous malformation. This case is reported with a review of relevant literature.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Malformações Arteriovenosas
/
Pele
/
Telangiectasia Hemorrágica Hereditária
/
Telangiectasia
/
Epistaxe
/
Período Pós-Parto
/
Dispneia
/
Período Periparto
/
Insuficiência Cardíaca
/
Coreia (Geográfico)
Limite:
Adulto
/
Feminino
/
Humanos
País/Região como assunto:
Ásia
Idioma:
Coreano
Revista:
The Korean Journal of Hepatology
Ano de publicação:
2000
Tipo de documento:
Artigo
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