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Erschienen in: European Journal of Clinical Microbiology & Infectious Diseases 10/2017

03.06.2017 | Original Article

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

verfasst von: L. Larsen, C. R. Marker, A. D. Kjeldsen, F. R. Poulsen

Erschienen in: European Journal of Clinical Microbiology & Infectious Diseases | Ausgabe 10/2017

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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.
Literatur
4.
Zurück zum Zitat Koopmans MM, Brouwer MC, Geldhoff M, Seron MV, Houben J, van der Ende A et al (2014) Cerebrospinal fluid inflammatory markers in patients with Listeria monocytogenes meningitis. BBA Clin 44–51. doi:10.1016/j.bbacli.2014.06.001 Koopmans MM, Brouwer MC, Geldhoff M, Seron MV, Houben J, van der Ende A et al (2014) Cerebrospinal fluid inflammatory markers in patients with Listeria monocytogenes meningitis. BBA Clin 44–51. doi:10.​1016/​j.​bbacli.​2014.​06.​001
5.
Zurück zum Zitat Kjeldsen AD, Tørring PM, Nissen H, Andersen PE (2014) Cerebral abscesses among Danish patients with hereditary haemorrhagic telangiectasia. Acta Neurol Scand 129(3):192–197. doi:10.1111/ane.12167 CrossRefPubMed Kjeldsen AD, Tørring PM, Nissen H, Andersen PE (2014) Cerebral abscesses among Danish patients with hereditary haemorrhagic telangiectasia. Acta Neurol Scand 129(3):192–197. doi:10.​1111/​ane.​12167 CrossRefPubMed
6.
Zurück zum Zitat Dupuis-Girod S, Giraud S, Decullier E, Lesca G, Cottin V, Faure F et al (2007) Hemorrhagic hereditary telangiectasia (Rendu–Osler disease) and infectious diseases: an underestimated association. Clin Infect Dis 44(6):841–845. doi:10.1086/511645 CrossRefPubMed Dupuis-Girod S, Giraud S, Decullier E, Lesca G, Cottin V, Faure F et al (2007) Hemorrhagic hereditary telangiectasia (Rendu–Osler disease) and infectious diseases: an underestimated association. Clin Infect Dis 44(6):841–845. doi:10.​1086/​511645 CrossRefPubMed
8.
Zurück zum Zitat Shovlin CL, Jackson JE, Bamford KB, Jenkins IH, Benjamin AR, Ramadan H et al (2008) Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. Thorax 63(3):259–266. doi:10.1136/thx.2007.087452 CrossRefPubMed Shovlin CL, Jackson JE, Bamford KB, Jenkins IH, Benjamin AR, Ramadan H et al (2008) Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. Thorax 63(3):259–266. doi:10.​1136/​thx.​2007.​087452 CrossRefPubMed
10.
12.
Zurück zum Zitat Gallione CJ, Repetto GM, Legius E, Rustgi AK, Schelley SL, Tejpar S et al (2004) A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet 363(9412):852–859. doi:10.1016/s0140-6736(04)15732-2 CrossRefPubMed Gallione CJ, Repetto GM, Legius E, Rustgi AK, Schelley SL, Tejpar S et al (2004) A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet 363(9412):852–859. doi:10.​1016/​s0140-6736(04)15732-2 CrossRefPubMed
13.
Zurück zum Zitat Johnson DW, Berg JN, Gallione CJ, McAllister KA, Warner JP, Helmbold EA et al (1995) A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. Genome Res 5(1):21–28. doi:10.1101/gr.5.1.21 CrossRefPubMed Johnson DW, Berg JN, Gallione CJ, McAllister KA, Warner JP, Helmbold EA et al (1995) A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. Genome Res 5(1):21–28. doi:10.​1101/​gr.​5.​1.​21 CrossRefPubMed
14.
Zurück zum Zitat Lesca G, Plauchu H, Coulet F, Lefebvre S, Plessis G, Odent S et al (2004) Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France. Hum Mutat 23(4):289–299. doi:10.1002/humu.20017 CrossRefPubMed Lesca G, Plauchu H, Coulet F, Lefebvre S, Plessis G, Odent S et al (2004) Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France. Hum Mutat 23(4):289–299. doi:10.​1002/​humu.​20017 CrossRefPubMed
15.
Zurück zum Zitat McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE et al (1994) Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 8(4):345–351. doi:10.1038/ng1294-345 CrossRefPubMed McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE et al (1994) Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 8(4):345–351. doi:10.​1038/​ng1294-345 CrossRefPubMed
16.
17.
Zurück zum Zitat Tørring PM, Brusgaard K, Ousager LB, Andersen PE, Kjeldsen AD (2014) National mutation study among Danish patients with hereditary haemorrhagic telangiectasia. Clin Genet 86(2):123–133. doi:10.1111/cge.12269 CrossRefPubMed Tørring PM, Brusgaard K, Ousager LB, Andersen PE, Kjeldsen AD (2014) National mutation study among Danish patients with hereditary haemorrhagic telangiectasia. Clin Genet 86(2):123–133. doi:10.​1111/​cge.​12269 CrossRefPubMed
20.
Zurück zum Zitat Vase P (1988) Disputats: Telangiectasia haemorrhagica hereditaria, Mb. Osler. Department of Otorhinolaryngology, Odense University Hospital; University of Southern Denmark Vase P (1988) Disputats: Telangiectasia haemorrhagica hereditaria, Mb. Osler. Department of Otorhinolaryngology, Odense University Hospital; University of Southern Denmark
21.
Zurück zum Zitat Gallitelli M, Guastamacchia E, Resta F, Guanti G, Sabbà C (2006) Pulmonary arteriovenous malformations, hereditary hemorrhagic telangiectasia, and brain abscess. Respiration 73(4):553–557. doi:10.1159/000087150 CrossRefPubMed Gallitelli M, Guastamacchia E, Resta F, Guanti G, Sabbà C (2006) Pulmonary arteriovenous malformations, hereditary hemorrhagic telangiectasia, and brain abscess. Respiration 73(4):553–557. doi:10.​1159/​000087150 CrossRefPubMed
23.
Zurück zum Zitat Laulajainen-Hongisto A, Lempinen L, Färkkilä E, Saat R, Markkola A, Leskinen K et al (2016) Intracranial abscesses over the last four decades; changes in aetiology, diagnostics, treatment and outcome. Infect Dis (Lond) 48(4):310–316. doi:10.3109/23744235.2015.1113557 CrossRef Laulajainen-Hongisto A, Lempinen L, Färkkilä E, Saat R, Markkola A, Leskinen K et al (2016) Intracranial abscesses over the last four decades; changes in aetiology, diagnostics, treatment and outcome. Infect Dis (Lond) 48(4):310–316. doi:10.​3109/​23744235.​2015.​1113557 CrossRef
24.
Zurück zum Zitat Faughnan ME, Palda VA, Garcia-Tsao G, Geisthoff UW, McDonald J, Proctor DD et al (2011) International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet 48(2):73–87. doi:10.1136/jmg.2009.069013 CrossRefPubMed Faughnan ME, Palda VA, Garcia-Tsao G, Geisthoff UW, McDonald J, Proctor DD et al (2011) International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet 48(2):73–87. doi:10.​1136/​jmg.​2009.​069013 CrossRefPubMed
Metadaten
Titel
Prevalence of hereditary hemorrhagic telangiectasia in patients operated for cerebral abscess: a retrospective cohort analysis
verfasst von
L. Larsen
C. R. Marker
A. D. Kjeldsen
F. R. Poulsen
Publikationsdatum
03.06.2017
Verlag
Springer Berlin Heidelberg
Erschienen in
European Journal of Clinical Microbiology & Infectious Diseases / Ausgabe 10/2017
Print ISSN: 0934-9723
Elektronische ISSN: 1435-4373
DOI
https://doi.org/10.1007/s10096-017-3023-7

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