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Hereditary haemorrhagic telangiectasia: Young's procedure in the management of epistaxis

Published online by Cambridge University Press:  29 June 2007

A. A. Hosni*
Affiliation:
Department of Otolaryngology, Norfolk and Norwich Hosptial, Norwich.
A. J. Innes
Affiliation:
Department of Otolaryngology, Norfolk and Norwich Hosptial, Norwich.
*
Mr A. A. Hosni, F.R.C.S., Rosetta, Yester Park, Chislehurst, Kent BR7 5DQ.

Abstract

Two cases of hereditary haemorrhagic telangiectasia are presented. Epistaxis was intractable in both patients. Young's procedure proved successful in controlling nose bleeds. One of the patients has been followed-up for 14 years. Methods of treatment are discussed with a review of the literature.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 1994

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References

Babington, B. G. (1865) Hereditary epistaxis. Lancet 2: 362363.Google Scholar
Blackburn, E. K. (1963) Long-term treatment of epistaxis with oestrogens. British Medical Journal 2: 159160.CrossRefGoogle ScholarPubMed
Bradbeer, W. H. (1969) Treatment of hereditary telangiectasia. Journal of Laryngology and Otology 83: 667669.CrossRefGoogle ScholarPubMed
Brooker, D. S., Cinnamond, M. J. (1991) Young';s procedure in the treatment of epistaxis. Journal of Laryngology and Otology 105: 847848.CrossRefGoogle ScholarPubMed
Hanes, F. M. (1909) Multiple hereditary telangiectases causing haemorrhage hereditary haemorrhagic telangiectasia). John Hopkins Hospital Bulletin 20: 6373.Google Scholar
Harrison, D. F. N. (1964) Familial haemorrhagic telangiectasia: 20 cases treated with systemic oestrogen. Quarterly Journal of Medicine New Series 129: 2538.Google Scholar
Ilium, P., Bjerring, P. (1988) Hereditary haemorrhagic telangiectasia treated by laser surgery. Rhinology 26: 1924.Google Scholar
Jahnke, V. (1970) infrastructure of hereditary telangiectasia. Archives of Otolaryngology 91: 262265.CrossRefGoogle Scholar
Kendall, B. E., Joyner, M., Grant, H. (1977) Hereditary haemorrhagic telangiectasia microembolization in the management of epistaxis. Clinical Otolaryngology 2: 249261.CrossRefGoogle ScholarPubMed
Koch, H. J., Escher, G. C., Lewis, J. S. (1952) Hormonal management of hereditary haemorrhagic telangiectasia. Journal of American Medical Association 149: 13761380.CrossRefGoogle Scholar
Kluger, P. B.Shapshay, S. ML, Hybels, R. L., Bohigian, R. K. (1987) Neodymium-YAG laser intranasal photocoagulation in hereditary hemorrhagic telangiectasia: an update report. Laryngoscope 97: 13971401.CrossRefGoogle ScholarPubMed
McCabe, W. P., Kelly, A. P. (1972) Management of epistaxis in Osler-Weber-Rendu disease. Recurrence of telangiectases within a nasal skin graft. Plastic and Reconstructive Surgery 50: 114118.CrossRefGoogle ScholarPubMed
Milton, C. M., Shotton, J. C., Premachandran, D. J., Woodward, B. M., Fabre, J. W., Sergeant, R. J. (1993) A new technique using cultured epithelial sheets for the management of epistaxis associated with hereditary haemorrhagic telangiectasia. Journal of Laryngology and Otology 107: 510513.CrossRefGoogle ScholarPubMed
Osier, W. (1901) On a family form of recurring epistaxis associated with multiple telangiectases of the skin and mucous membranes. John Hopkins Hospital Bulletin 12: 333337.Google Scholar
Rendu, M. (1896) Epistaxis repetees chez un sujet porteur de petits angiomes cutanes et muqueux. Bulletin Societe Medicine Hopital Paris 13: 731733.Google Scholar
Saunders, W. H. (1962) Hereditary haemorrhagic telangiectasia: its familial pattern, clinical characteristics and surgical treatment. Archives of Otolaryngology 76: 245260.CrossRefGoogle ScholarPubMed
Saunders, W. (1964) Hereditary haemorrhagic telangiectasia. Effective treatment of epistaxis by septal dermoplasty. Acta Otolaryngologica 58: 497502.CrossRefGoogle Scholar
Shah, J. T., Karnick, P. P., Chitale, A. R., Nadkarni, M. S. (1974) Partial or total closure of the nostrils in atrophic rhinitis. Archives of Otolaryngology 100: 196198.CrossRefGoogle ScholarPubMed
Sinha, S. N., Sardana, D. S., Rajvanshi, V. S. (1977) A nine year review of 273 cases of atrophic rhinitis and its management. Journal of Laryngology and Otolgy 91: 591600.CrossRefGoogle Scholar
Sutton, H. G. (1864) Epistaxis as an indication of impaired nutrition and of degeneration of the vascular system. Medical Mirror 1: 769781.Google Scholar
Van Cutsem, E. (1993) Georges Brohee Prize. Oestrogen-progesterone, a new therapy of bleeding gastrointestinal malformations. Acta-Gastroenterological Belgica 56: 210.Google Scholar
Van Cutsem, E., Rutgeerts, P., Geboes, K., Van Gompel, F, Vantrappen, G. (1988) Estrogen-progesterone treatment of Osler- Weber-Rendu disease. Journal of Clinical Gastroenterologv 10: 676679.CrossRefGoogle ScholarPubMed
Weber, F. P. (1907) Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages. Lancet 2: 160162.Google Scholar
Young, A. (1967) Closure of the nostrils in atrophic rhinitis. Journal of Laryngology and Otology 81: 515524.CrossRefGoogle ScholarPubMed