eMedicine Specialties > Vascular Surgery > Medical Topics
Osler-Weber-Rendu Disease: Workup
Updated: Dec 15, 2008
Workup
Laboratory Studies
CBC count, bleeding time, and coagulation profile findings may exclude a concurrent disorder or coagulopathy.
Imaging Studies
- Chest radiograph: Posteroanterior and lateral chest radiographs may reveal a mass of enlarged arteries and veins typical of pulmonary arteriovenous malformation (AVM). Commonly found in the posterior lung bases, these lesions may also be hidden by the diaphragm.
- CT scanning: Helical CT scanning has been advocated as a screening method for pulmonary AVM. However, detractors believe the radiation exposure is unnecessary and the cost is prohibitive.
- CT scanning of the head is indicated in the workup of stroke and brain abscess and may reveal AVM.
- Abdominal CT scanning may be useful for liver, kidney, and splenic lesions.
- Magnetic resonance imaging: MRI or magnetic resonance angiography (MRA) may be useful, when clinical suspicion is high, in identifying CNS lesions not observed with CT scanning.
- Angiography: Preoperative or pre-ablative assessment of pulmonary AVM may warrant angiography for treatment planning. Mesenteric angiography may reveal a bleeding site or mesenteric AVM and facilitate appropriate surgical extirpation. As with other causes of GI bleeding, a hemorrhage rate of at least 1 mL/min is necessary for detection.
- Mesenteric angiography may reveal a bleeding site or mesenteric AVM and facilitate appropriate surgical extirpation. As with other causes of GI bleeding, a hemorrhage rate of at least 1 mL/min is necessary for detection.
- Cerebral angiography may be indicated in the preoperative workup of CNS lesions.
- Nuclear medicine bleeding scanning: GI bleeding of as little as 0.5 mL/min may be detected with technetium Tc 99m–labeled autologous RBC scanning.
- Contrast echocardiography: Contrast echocardiography has been shown to reveal pulmonary AVM when pulse oximetry examination or even pulmonary angiography findings were negative. Agitated saline, with its small air bubbles, creates visible contrast that can be observed in the left atrium on echocardiography. The presence of contrast in the left atrium indicates right-to-left shunt. The ability to detect intracardiac shunts is an advantage of this study over other shunt studies.55
Other Tests
- MR (magnetic resonance) angiography: Contrast-enhanced MRI scanning was shown to be appropriate for screening detection of pulmonary AVM. Planning for embolic treatment was possible with 3D reconstructed images.56
- Pulse oximetry: Orthodeoxia may be detected in patients with pulmonary AVM because of increased shunting of blood through lesions in inferior areas of the lung.57
- Oximetry is performed with the patient standing and supine for 10 minutes in each position.
- An oxygen saturation level of less than 96% in either position has been considered to indicate further testing.
- Screening for pulmonary AVM using pulse oximetry in conjunction with chest radiography has been recommended to be performed once in childhood, once after puberty, before pregnancy, and at 10-year intervals thereafter.58
- Additional shunt studies: Arterial blood gas examination can also be used as a screening test for pulmonary AVM. Technetium Tc 99m–tagged albumin microspheres have also been used for shunt detection.59
Diagnostic Procedures
- Endoscopy and push enteroscopy: Upper and lower GI endoscopy may reveal telangiectases or AVMs. Push enteroscopy allows visualization of proximal small bowel distal to the ligament of Treitz, although this or further intubation of the jejunum is technically demanding. Similarly, a skilled endoscopist can use a colonoscope placed proximal to the ileocecal valve to examine the distal ileum. Visualizing the entire small bowel with push enteroscopy is possible; however, general anesthesia and intraperitoneal access (laparotomy or laparoscopy) is needed to manipulate and thread the small bowel over the endoscope, which has been inserted via the mouth or rectum.
- Capsule endoscopy: This innovative relatively recent tool is useful in the evaluation of occult GI bleeding of small bowel origin. Telangiectases from HHT can be visualized with this approach.60 Using the capsule for diagnosis in a series of 18 patients, investigators noted small bowel involvement in patients with known gastric telangiectases in 56% of patients.61
Histologic Findings
Telangiectases manifest as focal dilatation of the postcapillary venules. Early lesions maintain a portion of intervening capillary bed. Perivascular lymphocytic infiltrate is observed. Fully developed lesions lack an intervening capillary bed. Markedly dilated arterioles and venules connect directly in a tortuous network. The mature lesion also shows lymphocytic infiltrate, as well as multiple layers of thickened smooth-muscle cells around connecting venules.62
More on Osler-Weber-Rendu Disease |
| Overview: Osler-Weber-Rendu Disease |
Workup: Osler-Weber-Rendu Disease |
| Treatment: Osler-Weber-Rendu Disease |
| Follow-up: Osler-Weber-Rendu Disease |
| Multimedia: Osler-Weber-Rendu Disease |
| References |
| « Previous Page | Next Page » |
References
Sutton HG. Epistaxis as an indication of impaired nutrition, and of degeneration of the vascular system. Med Mirror. 1864;769-81.
Babington BG. Hereditary epistaxis. Lancet. 1865;362-363.
Rendu M. Epistaxis repetees chez un sujet porteur de petits angiomes cutanes et muquex. Bull Mem Soc Med Hop Paris. 1896;13:731.
Osler W. On a family form of recurring epistaxis associated with multiple telangiectases of the skin and mucous membranes. Bull Johns Hopkins Hosp. 1901;12:333-7.
Weber FP. Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages. Lancet. 1907;ii:160-2.
Hanes FM. Multiple hereditary telangiectasis causing hemorrhage (hereditary hemorrhagic telangiectasia). Bull Johns Hopkins Hosp. 1909;20:63-73.
Shepherd JA. Angiomatous conditions of the gastro-intestinal tract. Br J Surg. Mar 1953;40(163):409-21. [Medline].
Guttmacher AE, Marchuk DA, White RI Jr. Hereditary hemorrhagic telangiectasia. N Engl J Med. Oct 5 1995;333(14):918-24. [Medline].
Haitjema TJ, van Snippenburg R, Disch FJ, Overtoom TT, Westermann CJ. [Recurrent epistaxis: sometimes Rendu-Osler-Weber disease]. Ned Tijdschr Geneeskd. Nov 2 1996;140(44):2157-60. [Medline].
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. Mar 1989;32(3):291-7. [Medline].
Porteous ME, Burn J, Proctor SJ. Hereditary haemorrhagic telangiectasia: a clinical analysis. J Med Genet. Aug 1992;29(8):527-30. [Medline].
Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu- Osler-Weber syndrome). Am J Med Genet. Mar 6 2000;91(1):66-7. [Medline].
Shovlin CL, Hughes JM. Hereditary hemorrhagic telangiectasia. N Engl J Med. Feb 1 1996;334(5):330-1; discussion 331-2. [Medline].
Shovlin CL, Letarte M. Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms. Thorax. Aug 1999;54(8):714-29. [Medline].
Cole SG, Begbie ME, Wallace GM, et al. A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5. J Med Genet. Jul 2005;42(7):577-82. [Medline].
Schoen FJ. Cotran RS, Vinay K, Collins T. Robbins Pathologic Basis of Disease. 5th. WB Saunders; 1994:509.
Kjeldsen AD, Oxhoj H, Andersen PE, et al. Pulmonary arteriovenous malformations: screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia. Chest. Aug 1999;116(2):432-9. [Medline].
Dakeishi M, Shioya T, Wada Y, et al. Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan. Hum Mutat. Feb 2002;19(2):140-8. [Medline].
Jessurun GA, Kamphuis DJ, van der Zande FH, et al. Cerebral arteriovenous malformations in The Netherlands Antilles. High prevalence of hereditary hemorrhagic telangiectasia-related single and multiple cerebral arteriovenous malformations. Clin Neurol Neurosurg. Sep 1993;95(3):193-8. [Medline].
Westermann CJ, Rosina AF, De Vries V, et al. The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: a family screening. Am J Med Genet A. Feb 1 2003;116A(4):324-8. [Medline].
Vase P, Grove O. Gastrointestinal lesions in hereditary hemorrhagic telangiectasia. Gastroenterology. Nov 1986;91(5):1079-83. [Medline].
McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, et al. Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet. Dec 1994;8(4):345-51. [Medline].
Johnson DW, Berg JN, Baldwin MA, Gallione CJ, Marondel I, Yoon SJ, et al. Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Nat Genet. Jun 1996;13(2):189-95. [Medline].
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. Mar 13 2004;363(9412):852-9. [Medline].
Braverman IM, Keh A, Jacobson BS. Ultrastructure and three-dimensional organization of the telangiectases of hereditary hemorrhagic telangiectasia. J Invest Dermatol. Oct 1990;95(4):422-7. [Medline].
van Laake LW, van den Driesche S, Post S, Feijen A, Jansen MA, Driessens MH, et al. Endoglin has a crucial role in blood cell-mediated vascular repair. Circulation. Nov 21 2006;114(21):2288-97. [Medline].
Fernandez-L A, Garrido-Martin EM, Sanz-Rodriguez F, Pericacho M, Rodriguez-Barbero A, Eleno N, et al. Gene expression fingerprinting for human hereditary hemorrhagic telangiectasia. Hum Mol Genet. Jul 1 2007;16(13):1515-33. [Medline].
Begbie ME, Wallace GM, Shovlin CL. Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century. Postgrad Med J. Jan 2003;79(927):18-24. [Medline].
Fulbright RK, Chaloupka JC, Putman CM, et al. MR of hereditary hemorrhagic telangiectasia: prevalence and spectrum of cerebrovascular malformations. AJNR Am J Neuroradiol. Mar 1998;19(3):477-84. [Medline].
Romer W, Burk M, Schneider W. [Hereditary hemorrhagic telangiectasia (Osler's disease)]. Dtsch Med Wochenschr. Apr 24 1992;117(17):669-75. [Medline].
AAssar OS, Friedman CM, White RI Jr. The natural history of epistaxis in hereditary hemorrhagic telangiectasia. Laryngoscope. Sep 1991;101(9):977-80. [Medline].
Garcia-Monaco R, Taylor W, Rodesch G, et al. Pial arteriovenous fistula in children as presenting manifestation of Rendu-Osler-Weber disease. Neuroradiology. Jan 1995;37(1):60-4. [Medline].
Krings T, Chng SM, Ozanne A, Alvarez H, Rodesch G, Lasjaunias PL. Hereditary hemorrhagic telangiectasia in children: endovascular treatment of neurovascular malformations: results in 31 patients. Neuroradiology. Dec 2005;47(12):946-54. [Medline].
Easey AJ, Wallace GM, Hughes JM, et al. Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life. J Neurol Neurosurg Psychiatry. Jun 2003;74(6):743-8. [Medline].
Maher CO, Piepgras DG, Brown RD Jr, et al. Cerebrovascular manifestations in 321 cases of hereditary hemorrhagic telangiectasia. Stroke. Apr 2001;32(4):877-82. [Medline].
Cloft HJ. Spontaneous regression of cerebral arteriovenous malformation in hereditary hemorrhagic telangiectasia. AJNR Am J Neuroradiol. Jun-Jul 2002;23(6):1049-50. [Medline].
Du R, Hashimoto T, Tihan T, et al. Growth and regression of arteriovenous malformations in a patient with hereditary hemorrhagic telangiectasia. Case report. J Neurosurg. Mar 2007;106(3):470-7. [Medline].
Leung KM, Agid R, terBrugge K. Spontaneous regression of a cerebral arteriovenous malformation in a child with hereditary hemorrhagic telangiectasia. Case report. J Neurosurg. Nov 2006;105(5 Suppl):428-31. [Medline].
Press OW, Ramsey PG. Central nervous system infections associated with hereditary hemorrhagic telangiectasia. Am J Med. Jul 1984;77(1):86-92. [Medline].
White RI Jr, Lynch-Nyhan A, Terry P, et al. Pulmonary arteriovenous malformations: techniques and long-term outcome of embolotherapy. Radiology. Dec 1988;169(3):663-9. [Medline].
Berg JN, Guttmacher AE, Marchuk DA, et al. Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin?. J Med Genet. Mar 1996;33(3):256-7. [Medline].
Cottin V, Chinet T, Lavolé A, et al. Pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia: a series of 126 patients. Medicine (Baltimore). Jan 2007;86(1):1-17. [Medline].
Pierucci P, Murphy J, Henderson KJ, et al. New definition and natural history of patients with diffuse pulmonary arteriovenous malformations: twenty-seven-year experience. Chest. Mar 2008;133(3):653-61. [Medline].
Trembath RC, Thomson JR, Machado RD, et al. Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia. N Engl J Med. Aug 2 2001;345(5):325-34. [Medline].
Proctor DD, Henderson KJ, Dziura JD, Longacre AV, White RI Jr. Enteroscopic evaluation of the gastrointestinal tract in symptomatic patients with hereditary hemorrhagic telangiectasia. J Clin Gastroenterol. Feb 2005;39(2):115-9. [Medline].
Abdalla SA, Geisthoff UW, Bonneau D, et al. Visceral manifestations in hereditary haemorrhagic telangiectasia type 2. J Med Genet. Jul 2003;40(7):494-502. [Medline].
van Cutsem E, Rutgeerts P, Vantrappen G. Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone. Lancet. Apr 21 1990;335(8695):953-5. [Medline].
Wu JS, Saluja S, Garcia-Tsao G, et al. Liver involvement in hereditary hemorrhagic telangiectasia: CT and clinical findings do not correlate in symptomatic patients. AJR Am J Roentgenol. Oct 2006;187(4):W399-405. [Medline].
Garcia-Tsao G. Liver involvement in hereditary hemorrhagic telangiectasia (HHT). J Hepatol. Mar 2007;46(3):499-507. [Medline].
Larson AM. Liver disease in hereditary hemorrhagic telangiectasia. J Clin Gastroenterol. Feb 2003;36(2):149-58. [Medline].
Garcia-Tsao G, Korzenik JR, Young L, et al. Liver disease in patients with hereditary hemorrhagic telangiectasia. N Engl J Med. Sep 28 2000;343(13):931-6. [Medline].
Alizad A, Seward JB. Echocardiographic features of genetic diseases: part 3. Shunts. J Am Soc Echocardiogr. Mar 2000;13(3):248-53. [Medline].
Shovlin CL, Sodhi V, McCarthy A, Lasjaunias P, Jackson JE, Sheppard MN. Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services. BJOG. Aug 2008;115(9):1108-15. [Medline].
Gershon AS, Faughnan ME, Chon KS, et al. Transcatheter embolotherapy of maternal pulmonary arteriovenous malformations during pregnancy. Chest. Feb 2001;119(2):470-7. [Medline].
Nanthakumar K, Graham AT, Robinson TI, et al. Contrast echocardiography for detection of pulmonary arteriovenous malformations. Am Heart J. Feb 2001;141(2):243-6. [Medline].
Schneider G, Uder M, Koehler M, et al. MR angiography for detection of pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia. AJR Am J Roentgenol. Apr 2008;190(4):892-901. [Medline].
Robin ED, Laman D, Horn BR, et al. Platypnea related to orthodeoxia caused by true vascular lung shunts. N Engl J Med. Apr 22 1976;294(17):941-3. [Medline].
Faughnan ME, Hyland RH, Nanthakumar K, et al. Screening in hereditary hemorrhagic telangiectasia patients. Chest. Aug 2000;118(2):566-7. [Medline].
Thompson RD, Jackson J, Peters AM, et al. Sensitivity and specificity of radioisotope right-left shunt measurements and pulse oximetry for the early detection of pulmonary arteriovenous malformations. Chest. Jan 1999;115(1):109-13. [Medline].
Hahne M, Riemann JF. Vascular Abnormalities. In: Atlas of Capsule Endoscopy. Given Imaging; 2002:Ch 7, 73-81.
Ingrosso M, Sabbà C, Pisani A, et al. Evidence of small-bowel involvement in hereditary hemorrhagic telangiectasia: a capsule-endoscopic study. Endoscopy. Dec 2004;36(12):1074-9. [Medline].
Jacobson BS. Hereditary hemorrhagic telangiectasia: A model for blood vessel growth and enlargement. Am J Pathol. Mar 2000;156(3):737-42. [Medline].
Rebeiz EE, Bryan DJ, Ehrlichman RJ, et al. Surgical management of life-threatening epistaxis in Osler-Weber-Rendu disease. Ann Plast Surg. Aug 1995;35(2):208-13. [Medline].
Shah RK, Dhingra JK, Shapshay SM. Hereditary hemorrhagic telangiectasia: a review of 76 cases. Laryngoscope. May 2002;112(5):767-73. [Medline].
Harvey RJ, Kanagalingam J, Lund VJ. The impact of septodermoplasty and potassium-titanyl-phosphate (KTP) laser therapy in the treatment of hereditary hemorrhagic telangiectasia-related epistaxis. Am J Rhinol. Mar-Apr 2008;22(2):182-7. [Medline].
Shovlin CL, Winstock AR, Peters AM, et al. Medical complications of pregnancy in hereditary haemorrhagic telangiectasia. QJM. Dec 1995;88(12):879-87. [Medline].
Lerut J, Orlando G, Adam R, et al. Liver transplantation for hereditary hemorrhagic telangiectasia: Report of the European liver transplant registry. Ann Surg. Dec 2006;244(6):854-62; discussion 862-4. [Medline].
Thevenot T, Vanlemmens C, Di Martino V, Becker MC, Denue PO, Kantelip B, et al. Liver transplantation for cardiac failure in patients with hereditary hemorrhagic telangiectasia. Liver Transpl. Jul 2005;11(7):834-8. [Medline].
Curie A, Lesca G, Cottin V, et al. Long-term follow-up in 12 children with pulmonary arteriovenous malformations: confirmation of hereditary hemorrhagic telangiectasia in all cases. J Pediatr. Sep 2007;151(3):299-306. [Medline].
Gedge F, McDonald J, Phansalkar A, et al. Clinical and analytical sensitivities in hereditary hemorrhagic telangiectasia testing and a report of de novo mutations. J Mol Diagn. Apr 2007;9(2):258-65. [Medline].
Dallas NA, Samuel S, Xia L, et al. Endoglin (CD105): a marker of tumor vasculature and potential target for therapy. Clin Cancer Res. Apr 1 2008;14(7):1931-7. [Medline].
Checketts SR, Burton PS, Bjorkman DJ, et al. Generalized essential telangiectasia in the presence of gastrointestinal bleeding. J Am Acad Dermatol. Aug 1997;37(2 Pt 2):321-5. [Medline].
Dhingra JK, Shah RK, Shapshay SM. Hereditary Hemorrhagic Telangiectasia: A Review of 67 Cases. American Laryngological, Rhinological and Otological Soc. Jan 2000.
Kjeldsen AD, Vase P, Green A. Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients. J Intern Med. Jan 1999;245(1):31-9. [Medline].
Kjeldsen AD, Vase P, Oxhoj H. Hereditary hemorrhagic telangiectasia. N Engl J Med. Feb 1 1996;334(5):331-2. [Medline].
Marchuk DA. The molecular genetics of hereditary hemorrhagic telangiectasia. Chest. Jun 1997;111(6 Suppl):79S-82S. [Medline].
Moussouttas M, Fayad P, Rosenblatt M, et al. Pulmonary arteriovenous malformations: cerebral ischemia and neurologic manifestations. Neurology. Oct 10 2000;55(7):959-64. [Medline].
Saba HI, Morelli GA, Logrono LA. Brief report: treatment of bleeding in hereditary hemorrhagic telangiectasia with aminocaproic acid. N Engl J Med. Jun 23 1994;330(25):1789-90. [Medline].
Further Reading
Keywords
Osler-Weber-Rendu disease, OWRD, Osler-Weber-Rendu syndrome, OWRS, hereditary hemorrhagic telangiectasia, HHT, Rendu-Osler-Weber disease, ROWD, pulmonary arterial venous malformation, PAVM, epistaxis, nosebleed, gastrointestinal bleeding, GI bleeding, contrast echocardiography, activin receptor-like kinase 1, ALK-1, endoglin, ENG, HHT-juvenile polyposis overlap syndrome, JPHT
Workup: Osler-Weber-Rendu Disease