Literature DB >> 28578477

Prevalence of hereditary hemorrhagic telangiectasia in patients operated for cerebral abscess: a retrospective cohort analysis.

L Larsen1,2, C R Marker3,4, A D Kjeldsen4,5, F R Poulsen3,5.   

Abstract

It is well described that patients with pulmonary arteriovenous malformations (PAVMs) and Hereditary Hemorrhagic Telangiectasia (HHT) have an increased risk of cerebral abscess (CA). However, as both CA and HHT are rare, the proportion of patients with CA who are diagnosed with HHT has not been previously described. A retrospective study was carried out of all patients treated surgically for CA between January 1995 and September 2014 at the Department of Neurosurgery, Odense University Hospital. The cases were then cross-referenced with the Danish HHT database. Eighty patients aged 5-79 years were included. The incidence of CA was 0.33/100,000/year. Two patients (2.5%) were registered as having HHT. Bacterial pathogens were identified in 70% of all cases, most frequently streptococci species (46.3%). The most common predisposing condition was odontogenic infection (20%), followed by post-operative infection (13.8%) and post-trauma (6.3%). Patients undergoing a full diagnostic program to determine predisposing conditions causing CA increased over the 20-year period from 11.8% to 65.2%. The 3-month and 1-year mortality rates were 7.5% and 11.25%, respectively. There is an overrepresentation of HHT patients in a cohort of patients with CA, and HHT should be investigated as the cause of the CA if no other apparent cause can be identified.

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Year:  2017        PMID: 28578477     DOI: 10.1007/s10096-017-3023-7

Source DB:  PubMed          Journal:  Eur J Clin Microbiol Infect Dis        ISSN: 0934-9723            Impact factor:   3.267


  24 in total

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Authors:  Matthijs C Brouwer; Allan R Tunkel; Guy M McKhann; Diederik van de Beek
Journal:  N Engl J Med       Date:  2014-07-31       Impact factor: 91.245

2.  Pulmonary arteriovenous malformations, hereditary hemorrhagic telangiectasia, and brain abscess.

Authors:  Mauro Gallitelli; Edoardo Guastamacchia; Francesco Resta; Ginevra Guanti; Carlo Sabbà
Journal:  Respiration       Date:  2005-07-21       Impact factor: 3.580

3.  Cerebral abscess. Aetiology and pathogenesis, symptoms, diagnosis and treatment. A review of 200 cases from 1935-1976.

Authors:  H Nielsen; C Gyldensted; A Harmsen
Journal:  Acta Neurol Scand       Date:  1982-06       Impact factor: 3.209

4.  National mutation study among Danish patients with hereditary haemorrhagic telangiectasia.

Authors:  P M Tørring; K Brusgaard; L B Ousager; P E Andersen; A D Kjeldsen
Journal:  Clin Genet       Date:  2013-10-03       Impact factor: 4.438

5.  High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients.

Authors:  Claudia Schulte; Urban Geisthoff; Andreas Lux; Susan Kupka; Hans-Peter Zenner; Nikolaus Blin; Markus Pfister
Journal:  Hum Mutat       Date:  2005-06       Impact factor: 4.878

6.  A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.

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Journal:  Genome Res       Date:  1995-08       Impact factor: 9.043

7.  Cerebrovascular manifestations in 321 cases of hereditary hemorrhagic telangiectasia.

Authors:  C O Maher; D G Piepgras; R D Brown; J A Friedman; B E Pollock
Journal:  Stroke       Date:  2001-04       Impact factor: 7.914

8.  Intracranial abscesses over the last four decades; changes in aetiology, diagnostics, treatment and outcome.

Authors:  Anu Laulajainen-Hongisto; Laura Lempinen; Esa Färkkilä; Riste Saat; Antti Markkola; Kimmo Leskinen; Göran Blomstedt; Antti A Aarnisalo; Jussi Jero
Journal:  Infect Dis (Lond)       Date:  2015-11-23

9.  Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.

Authors:  K A McAllister; K M Grogg; D W Johnson; C J Gallione; M A Baldwin; C E Jackson; E A Helmbold; D S Markel; W C McKinnon; J Murrell
Journal:  Nat Genet       Date:  1994-12       Impact factor: 38.330

10.  Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France.

Authors:  Gaëtan Lesca; Henri Plauchu; Florence Coulet; Sylvain Lefebvre; Ghislaine Plessis; Sylvie Odent; Sophie Rivière; Bruno Leheup; Cyril Goizet; Marie-France Carette; Jean-François Cordier; Stéphane Pinson; Florent Soubrier; Alain Calender; Sophie Giraud
Journal:  Hum Mutat       Date:  2004-04       Impact factor: 4.878

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  2 in total

1.  Life-Threatening Intraventricular Rupture of Brain Abscess in a Patient With Undiagnosed Hereditary Hemorrhagic Telangiectasia.

Authors:  Christopher M Nguyen; Jessica Stauber; Michelle Baliss; David Reynoso
Journal:  Cureus       Date:  2020-06-21

2.  Positive predictive value of ICD-10 diagnosis codes for brain abscess in the Danish National Patient Registry.

Authors:  Jacob Bodilsen; Michael Dalager-Pedersen; Nicolai Kjærgaard; Diederik van de Beek; Matthijs C Brouwer; Henrik Nielsen
Journal:  Clin Epidemiol       Date:  2018-10-12       Impact factor: 4.790

  2 in total

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