Subscribe to RSS
DOI: 10.1055/s-2004-826045
Evidence of Small-Bowel Involvement in Hereditary Hemorrhagic Telangiectasia: a Capsule-Endoscopic Study
Publication History
Submitted 23 January 2004
Accepted after Revision 11 August 2004
Publication Date:
01 December 2004 (online)
Background and Study Aims: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal-dominant vascular disorder leading to telangiectases and arteriovenous malformations of the skin, mucosa, and viscera. Telangiectases in the upper gastrointestinal tract are known, but data regarding possible small-bowel involvement are scarce due to the technical difficulty of exploring the entire gastrointestinal tract. The aim of the present study was to use capsule endoscopy (CE) to determine the prevalence of small-bowel telangiectases in HHT patients.
Patients and Methods: From December 2001 to September 2002, 20 consecutive adult HHT patients at an interdepartmental HHT center were prospectively evaluated. All patients underwent esophagogastroduodenoscopy (EGD) followed by CE within 24 h. The telangiectases were scored according to commonly accepted criteria by two endoscopists and two observers of the video-capsule images, who were blinded to each other’s findings.
Results: EGD revealed gastric telangiectases in 15 of the 20 patients (75 %), while CE demonstrated small-bowel involvement in 10 of 18 patients (56 %; images were not recorded for two patients due to battery failure). No preferential site for telangiectasia was found between the jejunum and the terminal ileum. All patients who were positive on CE were also found to have gastric involvement at EGD. Patients with small-bowel telangiectases were significantly older than those without (62.5 years vs. 45 years; P < 0.02).
Conclusions: This study established a 56 % prevalence of small-bowel telangiectases in patients with HHT. This new endoscopic technique will probably change the etiological diagnosis of occult bleeding in HHT patients (which is too often attributed only to epistaxis) and may also be able to alter treatment strategies in HHT patients with gastrointestinal bleeding.
References
- 1 Guttmacher A E, Marchuk D A, White R I Jr. Hereditary hemorrhagic telangiectasia. N Engl J Med. 1995; 333 918-924
- 2 Johnson D W, Berg J N, Baldwin M A. et al . Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Nat Genet. 1996; 13 189-195
- 3 Wallace G M, Shovlin C L. A hereditary haemorrhagic telangiectasia family with pulmonary involvement is unlinked to the known HHT genes, endoglin and ALK-1. Thorax. 2000; 55 685-690
- 4 Porteous M E, Burn J, Proctor S J. Hereditary haemorrhagic telangiectasia: a clinical analysis. J Med Genet. 1992; 29 527-530
- 5 Braverman I M, Keh A, Jacobson B S. Ultrastructure and three-dimensional organization of the telangiectases of hereditary hemorrhagic telangiectasia. J Invest Dermatol. 1990; 95 422-427
- 6 McDonald M T, Papenberg K A, Ghosh S. et al . A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34. Nat Genet. 1994; 6 197-204
- 7 Piantanida M, Buscarini E, Dellavecchia C. et al . Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2. J Med Genet. 1996; 33 441-443
- 8 Lastella P, Sabbà C, Lenato G. et al . Endoglin gene mutations and polymorphism in Italian patients with hereditary hemorrhagic telangiectasia. Clin Genet. 2003; 63 536-540
- 9 Kjeldesen A D, Vase P, Green A. Hereditary hemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients. J Intern Med. 1999; 245 31-39
- 10 Smith C R, Bartholomew L G, Cain J C. Hereditary hemorrhagic telangiectasia and gastrointestinal hemorrhage. Gastroenterology. 1963; 44 1-6
- 11 Vase P, Grove O. Gastrointestinal lesions in hereditary hemorrhagic telangiectasia. Gastroenterology. 1986; 91 1079-1083
- 12 Porteous M E, Curtis A, Williams O. et al . Genetic heterogeneity in hereditary haemorrhagic telangiectasia. J Med Genet. 1994; 31 925-926
- 13 Kjeldesen A D, Kjeldesen J. Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia. Am J Gastroenterol. 2000; 95 415-418
- 14 Fiorito J J, Brandt L J, Kozicky O. et al . The diagnostic yield of superior mesenteric angiography: correlation with the pattern of gastrointestinal bleeding. Am J Gastroenterol. 1989; 84 878-881
- 15 Voeller G R, Bunch G, Britt L G. Use of technetium-labeled red blood cell scintigraphy in the detection and management of gastrointestinal hemorrhage. Surgery. 1991; 110 799-804
- 16 Van Gossum A, Schmit A. Enteroscopy and cautery for small intestinal angiodysplasia. Gastrointest Endosc. 1997; 45 216-217
- 17 Appleyard M, Fireman Z, Glukhovsky A. et al . A randomized trial comparing wireless capsule endoscopy with push enteroscopy for detection of small bowel lesions. Gastroenterology. 2000; 119 1431-1438
- 18 Schmit A, Gay F, Adler M. et al . Diagnostic efficacy of push-enteroscopy and long-term follow-up of patients with small bowel angiodysplasias. Dig Dis Sci. 1996; 41 2348-2352
- 19 Rossini F P, Pennario M. Small-bowel endoscopy. Endoscopy. 2002; 34 13-20
- 20 Lewis B S, Swain P. Capsule endoscopy in the evaluation of patients with suspected small intestinal bleeding: the results of the first clinical trial [abstract]. Gastrointest Endosc. 2001; 53 AB 70
- 21 Gong F, Swain P, Mills T. Wireless endoscopy. Gastrointest Endosc. 2000; 51 725-729
- 22 Rabenstein T, Krauss N, Hahn E G. et al . Wireless capsule endoscopy: beyond the frontiers of flexible gastrointestinal endoscopy. Med Sci Monit. 2002; 8 128-132
- 23 Sabbà C, Pasculli G, Cirulli A. et al . Rendu-Osler-Weber disease: experience with 56 patients. Ann Ital Med Int. 2002; 17 173-179
- 24 Ianora A A, Memeo M, Sabbà C. et al . Hereditary hemorrhagic telangiectasia: multi-detector row helical CT assessment of hepatic involvement. Radiology. 2004; 230 250-259
- 25 Shovlin C L, Guttmacher A E, Buscarini E. et al . Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet. 2000; 91 66-67
- 26 Inouye P, Marcon N, Pugash R A. et al . Embolization of a duodenal arteriovenous malformation in hereditary hemorrhagic telangiectasia: case report and review of the literature. Can J Gastroenterol. 2003; 17 661-665
- 27 Ell C, Remke S, May A. et al . The first prospective controlled trial comparing wireless capsule endoscopy with push enteroscopy in chronic gastrointestinal bleeding. Endoscopy. 2002; 34 685-689
- 28 Herrerias J M, Caunedo A, Rodriguez-Tellez M. et al . Capsule endoscopy in patients with suspected Crohn’s disease and negative endoscopy. Endoscopy. 2003; 35 564-568
- 29 Saurin J C, Delvaux M, Gaudin J L. et al . Diagnostic value of endoscopic capsule in patients with obscure digestive bleeding: blinded comparison with video push enteroscopy. Endoscopy. 2003; 35 576-584
- 30 Plauchu H, de Chadarevian J P, Bideau A, Robert J M. Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet. 1989; 32 291-297
- 31 Yamamoto H, Yano T, Kita H. et al . New system of double-balloon enteroscopy for diagnosis and treatment of small intestinal disorders. Gastroenterology. 2003; 125 1556-1557
C. Sabbà, M. D.
Dept. of Internal Medicine · University of Bari Hospital
Piazza Giulio Cesare 11 · Bari · Italy 70124
Fax: +39-080-5478708
Email: c.sabba@dimimp.uniba.it