Hemorrhagic hereditary telangiectasia (Rendu-Osler disease) and infectious diseases: An underestimated association

Clinical Infectious Diseases

Volumn 44, Issue 6, 2007, Pages 841-845

  Dupuis Girod, Sophie ^a   Giraud, Sophie ^b   Decullier, Evelyne ^c   Lesca, Gaetan ^b   Cottin, Vincent ^c   Faure, Frédéric ^b   Merrot, Olivier ^d   Saurin, Jean Christophe ^e   Cordier, Jean François ^c   Plauchu, Henri ^a  

^a HÔTEL DIEU   (France)

^b EDOUARD HERRIOT HOSPITAL   (France)

^c LOUIS PRADEL HOSPITAL   (France)

^d CROIX ROUSSE HOSPITAL   (France)

^e UNIVERSITÉ LYON 1   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ANAEROBIC BACTERIUM; ARTERIOVENOUS MALFORMATION; ARTICLE; BRAIN INFECTION; DISEASE ASSOCIATION; EPISTAXIS; FEMALE; HUMAN; INFECTION; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE; SCHOOL CHILD; STAPHYLOCOCCUS AUREUS;

ADOLESCENT; ADULT; AGE DISTRIBUTION; AGED; AGED, 80 AND OVER; CHILD; COHORT STUDIES; COMMUNICABLE DISEASES; COMORBIDITY; FEMALE; FRANCE; HUMANS; INCIDENCE; MALE; MIDDLE AGED; PROGNOSIS; RETROSPECTIVE STUDIES; RISK ASSESSMENT; SEVERITY OF ILLNESS INDEX; SEX DISTRIBUTION; SURVIVAL ANALYSIS; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

EID: 33847620295     PISSN: 10584838     EISSN: None     Source Type: Journal    
DOI: 10.1086/511645     Document Type: Article

References (22)

1. Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000; 91:66-7.
2. Gallione CJ, Repetto GM, Legius E, et al. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet 2004; 363:852-9.
3. Cole SG, Begbie ME, Wallace GM, Shovlin CL. A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5. J Med Genet 2005; 42:577-82.
4. McAllister KA, Grogg KM, Johnson DW, et al. Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 1994; 8:345-51.
5. Jirillo E, Amati L, Suppressa P, et al. Involvement of the transforming growth factor beta in the pathogenesis of hereditary hemorrhagic telangiectasia. Curr Pharm Des 2006; 12:1195-200.
6. Fernandez LA, Sanz-Rodriguez F, Blanco FJ, Bernabeu C, Botella LM. Hereditary hemorrhagic telangiectasia, a vascular dysplasia affecting the TGF-beta signaling pathway. Clin Med Res 2006; 4:66-78.
7. Gallitelli M, Lepore V, Pasculli G, et al. Brain abscess: a need to screen for pulmonary arteriovenous malformations. Neuroepidemiology 2005; 24:76-8.
8. Blanco P, Schaeverbeke T, Baillet L, Lequen L, Bannwarth B, Dehais J. Rendu-Osler familial telangiectasia angiomatosis and bacterial spondylodiscitis [in French]. Rev Med Interne 1998; 19:938-9.
9. Duval X, Djendli S, Le Moing V, et al. Recurrent Staphylococcus aureus extracerebral infections complicating hereditary hemorrhagic telangiectasia (Osler-Rendu-Weber disease). Am J Med 2001; 110:671-2.
10. Cirulli A, Loria MP, Dambra P, et al. Patients with hereditary hemorrhagic telangectasia (HHT) exhibit a deficit of polymorphonuclear cell and monocyte oxidative burst and phagocytosis: a possible correlation with altered adaptive immune responsiveness in HHT. Curr Pharm Des 2006; 12:1209-15.
11. Cottin V, Plauchu H, Bayle JY, Barthelet M, Revel D, Cordier JF. Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia. Am J Respir Crit Care Med 2004; 169:994-1000.
12. Buscarini E, Danesino C, Olivieri C, et al. A. Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia-results of extensive screening. Ultraschall Med 2004; 25:348-55.
13. Lesca G, Plauchu H, Coulet F, et al. Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France. Hum Mutat 2004; 23:289-99.
14. Danai P, Martin GS. Epidemiology of sepsis: recent advances. Curr Infect Dis Rep 2005; 7:329-34.
15. Tiemersma EW, Monnet DL, Bruinsma N, Skov R, Monen JC, Grundmann H. Staphylococcus aureus bacteremia, Europe. Emerg Infect Dis 2005; 11:1798-9.
16. Gallitelli M, Guastamacchia E, Resta F, Guanti G, Sabba C. Pulmonary arteriovenous malformations, hereditary hemorrhagic telangiectasia, and brain abscess. Respiration 2006; 73:553-7.
17. Gossage JR, Kanj G. Pulmonary arteriovenous malformations: a state of the art review. Am J Respir Crit Care Med 1998; 158:643-61.
18. Engelhardt K, Kampfl A, Spiegel M, Pfausler B, Hausdorfer H, Schmutzhard E. Brain abscess due to Capnocytophaga species, Actinomyces species, and Streptococcus intermedius in a patient with cyanotic congenital heart disease. Eur J Clin Microbiol Infect Dis 2002; 21:236-7.
19. Davis JP, Chesney PJ, Wand PJ, LaVenture M. Toxic-shock syndrome: epidemiologic features, recurrence, risk factors, and prevention. N Engl J Med 1980; 303:1429-35.
20. Hull HF, Mann JM, Sands CJ, Gregg SH, Kaufman PW. Toxic shock syndrome related to nasal packing. Arch Otolaryngol 1983; 109:624-6.
21. Ashcroft GS. Bidirectional regulation of macrophage function by TGF-beta. Microbes Infect 1999; 1:1275-82.
22. Blanco P. Analysis of lymphocytes subset in a series of 39 HHT patients. In: Program and abstracts of the 6th HHT Scientific Conference (Lyon, France). 2005:54.