Pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia
نویسندگان
چکیده
منابع مشابه
Neonatal pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia.
A 3 week old infant presented with persistent hypoxaemia and was diagnosed with pulmonary arteriovenous malformations. Her family history was positive for hereditary haemorrhagic telangiectasia. She was treated successfully with coil embolotherapy at the age of 4 months. Transcatheter embolisation may be considered the primary treatment for pulmonary arteriovenous malformations in infancy.
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A non-smoker 61-year-old man presented with insidious shortness of breath and a history of chronic epistaxis for approximately three decades. The initial investigation revealed right basal crackles at auscultation, very subtle oral telangiectasia and a microcytic anaemia. A chest radiograph (Fig. 1A) demonstrated right basal rounded opacities communicating with the hilum. Further computed tomog...
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Hereditary haemorrhagic telangiectasia is a rare disease. Hepatic involvement is infrequent. A patient with an extensive hepatic arteriovenous malformation is presented. Characteristic computed tomographic and angiographic findings are described followed by a review of the literature.
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Pulmonary arteriovenous malformations (PAVMs) are vascular structures that provide a direct capillary-free communication between the pulmonary and systemic circulations. The majority of patients have no PAVM-related symptoms, but are at risk of major complications that can be prevented by appropriate interventions. More than 90% of PAVMs occur as part of hereditary haemorrhagic telangiectasia (...
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A 41-year-old woman with a history of recurrent epistaxis presented with left hemiplegia, right gaze deviation, and dysarthria. Physical examination confirmed skin and lip telangiectasia (figure 1). Her son had pulmonary arteriovenous malformation (AVM). Her head CT and cerebral angiography revealed right parietal hemorrhage with parasagittal AVM (figure 2). Hereditary hemorrhagic telangiectasi...
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2019
ISSN: 1757-790X
DOI: 10.1136/bcr-2018-228456