Literature DB >> 11267812

Brain abscess in patients with hereditary hemorrhagic telangiectasia: case report and literature review.

S L Dong1, S F Reynolds, I P Steiner.   

Abstract

Hereditary hemorrhagic telangiectasia (HHT), or Osler-Weber-Rendu disease, affects multiple organ systems. Brain abscess is a potential complication, and this disease carries a high mortality. In the setting of HHT the abscess most likely results from paradoxical septic emboli or bacterial seeding of an ischemic portion of the brain after paradoxical sterile emboli. Brain abscess is the diagnosis that must be ruled out in patients with HHT presenting with new onset neurologic symptoms. The clinician can be misled by seemingly benign and nonspecific symptoms, signs, and laboratory test results. Appropriate diagnostic imaging with computed tomography or magnetic resonance imaging of the head is mandatory. We present a case of brain abscess in a patient with HHT presenting to the Emergency Department. The review of the literature deals with the pathophysiology and manifestations of HHT with particular focus on the pathologic and clinical features, and management of cerebral abscess in this setting. Differences between patients with brain abscess with or without HHT are highlighted.

Entities:  

Mesh:

Year:  2001        PMID: 11267812     DOI: 10.1016/s0736-4679(00)00315-2

Source DB:  PubMed          Journal:  J Emerg Med        ISSN: 0736-4679            Impact factor:   1.484


  6 in total

1.  Brain abscess as an initial presentation in a patient of hereditary haemorrhagic telangiectasia caused by a novel ENG mutation.

Authors:  Kai-Hsiang Chen; Chin-Hsien Lin
Journal:  BMJ Case Rep       Date:  2013-02-25

2.  Screening in cryptogenic brain abscess: Do not forget pulmonary arteriovenous malformations.

Authors:  Jasmien Rens; Thomas Van Thielen; Aurelie Derweduwen; Koen Goedseels; Robert Hes; Lars de Jong
Journal:  Surg Neurol Int       Date:  2021-04-26

3.  Hereditary hemorrhagic telangiectasia patient presenting with brain abscess due to silent pulmonary arteriovenous malformation.

Authors:  Marios Themistocleous; Dimitrios Giakoumettis; Andreas Mitsios; Christos Anagnostopoulos; Aristoteles Kalyvas; Christos Koutsarnakis
Journal:  Pan Afr Med J       Date:  2016-11-11

Review 4.  Hereditary hemorrhagic telangiectasia: diagnosis and management from the hematologist's perspective.

Authors:  Athena Kritharis; Hanny Al-Samkari; David J Kuter
Journal:  Haematologica       Date:  2018-05-24       Impact factor: 9.941

5.  Case Report: Clinical characteristics and genetic analysis of two patients with hereditary hemorrhagic telangiectasia.

Authors:  Qiu-Ying Wang; Yu-Xuan Feng; Ying-Wei Zhu; Yu-Xia Sun; Jing-Duan Xu; Hui-Min Shi; Yi-Min Mao; Hong-Wei Jiang
Journal:  Front Genet       Date:  2022-08-25       Impact factor: 4.772

6.  Orthodeoxia without Platypnea in Hereditary Hemorrhagic Telangiectasia in the Presence of a Cerebral Abscess and Multiple Pulmonary Arteriovenous Malformations: Unusual Complications and Transcatheter Endovascular Treatment.

Authors:  Carlos Salazar; Jacky Bruce Blank; Veronica Palmero
Journal:  Case Rep Pulmonol       Date:  2017-10-12
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.