The liver in hereditary hemorrhagic telangiectasia (Weber-Rendu-Osler disease)

Scandinavian Journal of Gastroenterology

Volumn 34, Issue 12, 1999, Pages 1241-1246

  Weik, C ^a,b   Greiner, L ^a,b  

^a UNIVERSITY OF WITTEN HERDECKE   (Germany)

^b HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

Aneurysm; Arteriovenous malformations; Color Doppler sonography; Focal liver lesion; Liver cirrhosis; Telangiectasia; Ultrasonography

Indexed keywords

ALANINE AMINOTRANSFERASE; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; BILIRUBIN; GAMMA GLUTAMYLTRANSFERASE; HEMOGLOBIN;

ADULT; ANGIOGRAPHY; ARTICLE; CLINICAL ARTICLE; COLOR ULTRASOUND FLOWMETRY; COMPUTER ASSISTED TOMOGRAPHY; ECHOGRAPHY; FEMALE; HUMAN; LIVER; LIVER BIOPSY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE;

EID: 0033373079     PISSN: 00365521     EISSN: None     Source Type: Journal    
DOI: 10.1080/003655299750024779     Document Type: Article

References (28)

1. 1. Guttmacher AE, Marchuk DA, White RI Jr. Hereditary hemorrhagic teleangiectasia. N Engl J Med 1995;333:918-24.
2. 2. Meyer CT, Troncale FJ, Galloway S, Sheahan DG. Arteriovenous malformations of the bowel: an analysis of 22 cases and a review of the literature. Medicine 1981;60:36-48.
3. 3. Van Cutsem E, Rutgeerts P, Vantrappen G. Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone. Lancet 1990;335:953-5.
4. 4. Vase P, Grove O. Gastrointestinal lesions in hereditary hemorrhagic teleangiectasia. Gastroenterology 1986;4-5:765-86.
5. 5. Bernard G, Mion F, Henry L, Plauchu H, Paliard P. Hepatic involvement in hereditary hemorrhagic teleangiektasia: clinical, radiological, and hemodynamic studies of 11 cases. Gastroenterology 1993;105:482-7.
6. 6. Martini GA. The liver in hereditary hemorrhagic teleangiektasia. An inborn error of vascular structure with multiple manifestations. A reappraisal. Gut 1978;19:531-7.
7. 7. Selmair M, Cidlinsky K, Ell C, Hahn EG. Hämangiomatose der Leber bei Morbus Osler. Dtsch Med Wochenschr 1993;118:1015-9.
8. 8. Cooney T, Sweeney EC, Coll R, Greally M. Pseudocirrhosis in hereditary hemorrhagic teleangiektasia. J Clin Pathol 1977;30:1134-41.
9. 9. Shovlin CL, Hughes JMB, Tuddenham EGD. A gene for hereditary hemorrhagic teleangiektasia maps to chromosome 9q3. Nat Genet 1994;6:205-9.
10. 10. Johnson DW, Berg JN, Gallione CJ. A second locus for hereditary hemorrhagic teleangiektasia maps to chromosome 12. Genome Res 1995;5:21-8.
11. 11. McAIlister KA, Grogg KM, Johnson DW. Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary hemorrhagic teleangiektasia type I. Nat Genet 1994;8:345-51.
12. 12. Porteous MEM, Curtis A, Williams O, Marchuk D, Bhattacharya SS, Burn J. Genetic heterogeneity in hereditary hemorrhagic teleangiektasia. J Med Genet 1994;31:925-6.
13. 13. Plauchu H, Chadarevian J-P, Bideau A, Robert J-M. Age-related clinical profile of hereditary hemorrhagic teleangiektasia in an epidemiologically recruited population. Am J Med Genet 1989;32:291-7.
14. 14. Daly JJ, Schiller AL. The liver in hereditary hemorrhagic teleangiectasia. Am J Med 1976;60:723-6.
15. 15. Wanless IR, Gryfe A. Nodular transformation of the liver in hereditary hemorrhagic teleangiektasia. Arch Pathol Lab Med 1986;110:331-5.
16. 16. Burckhardt D, Stalder A, Ludin L, Bianchi L. Hyperdynamic circulatory state due to Osler-Weber-Rendu disease with intrahepatic arteriovenous fistulas. Am Heart J 1973;85:797.
17. 17. Radtke WE, Smith HC, Fulton RE, Adson MA. Misdiagnosis of atrial septal defect in patients with hereditary hemorrhagic teleangiektasia and hepatic arteriovenous fistulas. Am Heart J 1978;95:235.
18. 18. Ball NJ, Duggan MA. Hepatolithiasis in hereditary hemorrhagic teleangiektasia. Arch Pathol Lab Med 1990;114:423-5.
19. 19. Goes E, Tussenbroeck FV, Cottene F, Hulstaert J, Osteaux M. Osler's disease diagnosed by ultrasound. J Clin Ultrasound 1987;15:129-31.
20. 20. Cloogman HM, DiCapo RD. Hereditary hemorrhagic teleangiektasia: sonographic findings in the liver. Radiology 1984; 150:521-2.
21. 21.Varma DGK, Schoenberger SG, Kumra A, Agrawal N, Robinson A. Osler-Weber-Rendu disease: MR findings in the liver. J Comput Assist Tomogr 1989;13:134-5.
22. 22. Vilgrain V, Menu Y, Nahum H. Doppler sonography in Osler-Weber-Rendu disease. Am J Roengtenol 1991;157:413-4.
23. 23. Ralls PW, Johnson MB, Radin RD, Lee KP, Boswell WD. Hereditary hemorrhagic teleangiektasia: findings in the liver with color doppler sonography. Am J Roengtenol 1992;59:159-61.
24. 24. Nies AS, Evans GH, Shand GH. Regional hemodynamic effects of beta-adrenergic blockade with propanolol in the unanesthetized primate. Am Heart J 1973;85:97.
25. 25. Römer W, Burk M, Schneider W. Hereditäre hämorrhagische Teleangiektasie (Morbus Osler). Dtsch Med Wochenschr 1992;117:669-75.
26. 26. Mays ET, Christopherson WM, Barrows GH. Focal nodular hyperplasia of the liver. Am J Clin Pathol 1974;61:735-46.
27. 27. Allison DJ, Jordan H, Hennessy O. Therapeutic embolization of the hepatic artery; a review of 75 procedures. Lancet 1985;1:595-9.
28. 28. Zieren J, Buttemeyer R, Muller JM. Adjustable 'banding' of the hepatic artery in treatment of shunt-induced heart failure in Osler-Rendu-Weber disease. Chirurg 1998;69:639-41.