ArticleActa bio-medica : Atenei Parmensis2022
A challenging case of anemia, respiratory failure and seizures.
Article in Acta bio-medica : Atenei Parmensis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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4 authors at 4 institutions in 3 countries.
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Abstract
backgroundHemorrhagic Hereditary Telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is a rare genetic disorder characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations. AIM AND
methodsWe describe the case of a 64-year old woman in which radiology was useful to interpret an apparently unexplained constellation of symptoms.
resultsBrain MRI showing ischemic stroke, pulmonary angiography demonstrating arteriovenous malformations, and capsule endoscopy detecting telangiectasias in the jejunum, along with a clinical history of recurrent epistaxis, allowed us to diagnose HHT.
conclusionsHHT is rare and difficult to diagnose. Radiology can aid the clinical suspicion. www.actabiomedica.it.
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