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Inn Med (Heidelb) ; 65(1): 71-75, 2024 Jan.
Article in German | MEDLINE | ID: mdl-37418022

ABSTRACT

A 43-year-old female patient with a brain abscess and a complicated clinical course was diagnosed with hereditary haemorrhagic telangiectasia (HHT) at the Martin Zeitz Centre for Rare Diseases in Hamburg, Germany. The brain abscess was caused by pulmonary arteriovenous malformations (AVM), a typical finding in HHT. Patients with cryptogenic brain abscess should be screened for pulmonary AVM and HHT. This case report illustrates the importance of patient history and interdisciplinary exchange in patients with a broad clinical spectrum as well as interdisciplinary treatment in the case of complications of rare diseases.


Subject(s)
Arteriovenous Malformations , Brain Abscess , Telangiectasia, Hereditary Hemorrhagic , Female , Humans , Adult , Telangiectasia, Hereditary Hemorrhagic/complications , Rare Diseases/complications , Arteriovenous Malformations/complications , Lung , Brain Abscess/diagnostic imaging
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