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Pulmonary Hypertension Due to High-Output Heart Failure: Hereditary Hemorrhagic Telangiectasia.
Kiliçkiran Avci, Burçak; Soysal, Ali Ugur; Cerme, Emir; Kargin, Osman Aykan; Hatemi, Ali Ibrahim; Ar, Muhlis Cem; Öngen, Zeki.
Afiliação
  • Kiliçkiran Avci B; Department of Cardiology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
  • Soysal AU; Department of Cardiology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
  • Cerme E; Department of Internal Medicine, Division of Gastroenterology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
  • Kargin OA; Department of Radiology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
  • Hatemi AI; Department of Internal Medicine, Division of Gastroenterology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
  • Ar MC; Department of Internal Medicine, Division of Hematology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
  • Öngen Z; Department of Cardiology, Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Istanbul, Türkiye.
Turk Kardiyol Dern Ars ; 51(7): 493-497, 2023 10.
Article em En | MEDLINE | ID: mdl-37861254
Pulmonary hypertension (PH) is a complex disorder that should be managed with a multidisciplinary approach. Although most of the underlying causes of left heart disease can be easily diagnosed with cardiac imaging, some pathologies might necessitate careful investigation to go beyond the obvious. High-output heart failure (HF) due to arteriovenous malformation (AVMs) is an unnoticeable cause for HF and PH. Patients with hepatic AVMs should always be carefully evaluated with regard to hereditary hemorrhagic telangiectasia (HHT) since they can have multiple signs related to the other systems without any symptoms. In this case report, we discussed a patient who was initially diagnosed as PH associated with HF with preserved ejection fraction but eventually was found to have PH associated with high-output HF due to hereditary hemorrhagic telangiectasia (HHT, or Osler Weber Rendu syndrome) after detailed evaluation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Telangiectasia Hemorrágica Hereditária / Cardiopatias / Insuficiência Cardíaca / Hipertensão Pulmonar Limite: Humans Idioma: En Revista: Turk Kardiyol Dern Ars Assunto da revista: CARDIOLOGIA Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Telangiectasia Hemorrágica Hereditária / Cardiopatias / Insuficiência Cardíaca / Hipertensão Pulmonar Limite: Humans Idioma: En Revista: Turk Kardiyol Dern Ars Assunto da revista: CARDIOLOGIA Ano de publicação: 2023 Tipo de documento: Article