Idiopathic pulmonary arteriovenous malformations: Clinical and imaging characteristics

European Respiratory Journal

Volumn 38, Issue 2, 2011, Pages 368-375

  Wong, H H ^a   Chan, R P ^e   Klatt, R ^a   Faughnan, M E ^b,c,d  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b ST MICHAEL'S HOSPITAL   (Canada)

^c ST MICHAEL'S HOSPITAL   (Canada)

^d ST MICHAEL'S HOSPITAL   (Canada)

^e York Central Hospital Richmond Hill   (Canada)

Author keywords

Arteriovenous malformations; Embolisation; Hereditary haemorrhagic telangiectasia; Lung; Therapeutic

Indexed keywords

ADULT; AGED; ARTICLE; ARTIFICIAL EMBOLISM; BRAIN ABSCESS; CEREBROVASCULAR ACCIDENT; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; DYSPNEA; FEMALE; FOLLOW UP; GENETIC SCREENING; HEMOPTYSIS; HUMAN; LUNG LOBE; MALE; MEDICAL RECORD REVIEW; MIGRAINE; PRIORITY JOURNAL; PROGNOSIS; PULMONARY ARTERIOVENOUS FISTULA; RENDU OSLER WEBER DISEASE; THORAX RADIOGRAPHY;

ADULT; AGED; AGED, 80 AND OVER; ARTERIOVENOUS MALFORMATIONS; BRAIN ABSCESS; EMBOLIZATION, THERAPEUTIC; FEMALE; GENETIC TESTING; HEMOPTYSIS; HUMANS; MALE; MIDDLE AGED; MUTATION; OXYGEN; PULMONARY ARTERY; RETROSPECTIVE STUDIES; STROKE; TELANGIECTASIA, HEREDITARY HEMORRHAGIC; TREATMENT OUTCOME;

EID: 80051535927     PISSN: 09031936     EISSN: 13993003     Source Type: Journal    
DOI: 10.1183/09031936.00075110     Document Type: Article

References (37)

1. Faughnan ME, Granton JT, Young LH. The pulmonary vascular complications of hereditary haemorrhagic telangiectasia. Eur Respir J 2009; 33: 1186-1194.
2. Post MC, van Gent MW, Plokker HW, et al. Pulmonary arteriovenous malformations associated with migraine with aura. Eur Respir J 2009; 84: 882-887.
3. Gupta P, Mordin C, Curtis J, et al. Pulmonary arteriovenous malformations: effect of embolization on right-to-left shunt, hypoxemia, and exercise tolerance in 66 patients. Am J Roentgenol 2002; 179: 347-355. (Pubitemid 34785635)
4. Mager JJ, Overtoom TT, Blauw H, et al. Embolotherapy of pulmonary arteriovenous malformations: long-term results in 112 patients. J Vasc Interv Radiol 2004; 15; 451-456. (Pubitemid 38590868)
5. Pollak JS, Saluja S, Thabet A, et al. Clinical and anatomic outcomes after embolotherapy of pulmonary arteriovenous malformations. J Vasc Interv Radiol 2006; Jan, 17: 35-44.
6. Lange PA, Stoller JK. The hepatopulmonary syndrome. Ann Intern Med 1995; 122: 521-529.
7. de Faria JL, Czapski K, Ribierto, et al. Cyanosis in Manson's schistosomiasis: role of pulmonary schistosomatic arteriovenous fistulas. Am Heart J 1957; 54: 196-204.
8. Prager RL, Laws KH, Bender Jr HW. Arteriovenous fistula of the lung. Ann Thorac Surg 1983; 36: 231-239. (Pubitemid 13039851)
9. Taxman RM, Halloran MJ, Parker BM. Multiple pulmonary arteriovenous malformations in association with Fanconi's syndrome. Chest 1973; 64: 118-120.
10. Pierce JA, Reagan WP, Kimball RW. Unusual cases of pulmonary arteriovenous fistulas with a note on thyroid carcinoma as a cause. New Engl J Med 1959; 18: 901-907.
11. White RI Jr, Pollak JS, Wirth JA. Pulmonary arteriovenous malformations: diagnosis and transcatheter embolotherapy. J Vasc Interv Radiol 1996; 7: 787-804. (Pubitemid 126729603)
12. Faughnan ME, Lui YW, Wirth JA, et al. Diffuse pulmonary arteriovenous malformations: characteristics and prognosis. Chest 2000; 117: 31-38. (Pubitemid 30053616)
13. Faughnan ME, Palda VA, Garcia-Tsao G, et al. International guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia. J Med Genet 2011; 48: 73-87.
14. White RI Jr, Lynch-Nyhan A, Terry P, et al. Pulmonary arteriovenous malformations: techniques and long-term outcome of embolotherapy. Radiology 1988; 169: 663-669.
15. Rosenblatt M, Pollak JS, Fayad PB, et al. Pulmonary arteriovenous malformations: what size should be treated to prevent embolic stroke? Radiology 1992; 185: P134.
16. Swanson KL, Prakash UB, Stanson AW. Pulmonary arteriovenous fistulas: Mayo Clinic experience, 1982-1997. Mayo Clin Proc 1999; 74: 671-680. (Pubitemid 29321281)
17. Cottin V, Chinet T, Lavolé A, et al. Pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia. Medicine 2007; 86: 1-17. (Pubitemid 46104915)
18. Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000; 91: 66-67. (Pubitemid 30127562)
19. McAllister KA, Grogg KM, Johnson DW, et al. Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 1994; 8: 345-351.
20. Berg JN, Gallione CJ, Stenzel TT, et al. The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2. Am J Hum Genet 1997; 61: 60-67. (Pubitemid 27323324)
21. 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: 852-859. (Pubitemid 38368834)
22. Gallione CJ, Richards JA, Letteboer TG, et al. SMAD4 mutations found in unselected HHT patients. J Med Genet 2006; 43: 793-797. (Pubitemid 44654737)
23. van Gent MW, Post MC, Luermans JG, et al. Screening for pulmonary arteriovenous malformations using transthoracic contrast echocardiography: a prospective study. Eur Respir J 2009; 33: 85-91.
24. Parra JA, Bueno J, Zarauza J, et al. Graded contrast echocardiography in pulmonary arteriovenous malformations. Eur Respir J 2010; 35: 1279-1285.
25. Prasad V, Chan RP, Faughnan ME. Embolotherapy of pulmonary arteriovenous malformations: efficacy of platinum versus stainless steel coils. J Vasc Interv Radiol 2004; 15: 153-160. (Pubitemid 38248915)
26. Moussouttas M, Fayad P, Rosenblatt M, et al. Pulmonary arteriovenous malformations: cerebral ischemia and neurologic manifestations. Neurology 2000; 55: 959-964.
27. Dines DE, Seward JB, Bernatz PE. Pulmonary arteriovenous fistula. Mayo Clin Proc 1983; 58: 176-181.
28. Puskas JD, Allen MS, Moncure AC, et al. Pulmonary arteriovenous malformations: therapeutic options. Ann Thorac Surg 1993; 56: 253-258. (Pubitemid 23245131)
29. Jackson JE, Whyte MKB, Allison DJ, et al. Coil embolization of pulmonary arteriovenous malformations. Cor Vasa 1990; 32: 191-196. (Pubitemid 20375918)
30. Gossage JR, Kanj G. Pulmonary arteriovenous malformations: a state of the art review. Am J Respir Crit Care Med 1998; 158: 643-661. (Pubitemid 28378198)
31. Prigoda NL, Savas S, Abdalla SA, et al. Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations. J Med Genet 2006; 43: 722-728. (Pubitemid 44483914)
32. Wallace GM, Shovlin CL. A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1. Thorax 2000; 55: 685-690. (Pubitemid 30468225)
33. Bayrak-Toydemir P, McDonald J, Akarsu N, et al. A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7. Am J Med Genet A 2006; 140: 2155-2162. (Pubitemid 44522429)
34. Cole SG, Begbie ME, Wallace GM, et al. A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5. J Med Genet 2005; 42: 577-582. (Pubitemid 40993833)
35. Porteous ME, Burn J, Proctor SJ. Hereditary haemorrhagic telangiectasia: a clinical analysis. J Med Genet 1992; 29: 527-530.
36. Al-Saleh S, Mei-Zahav M, Faughnan ME, et al. Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia. Eur Respir J 2009; 34: 875-881.
37. Plauchu H, de Chadarevian JP, Bideau A, et al. Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet 1989; 32: 291-297. (Pubitemid 19146524)