Long-term results of dermatoplasty in the treatment of hereditary haemorrhagic telangiectasia
- 1 January 1983
- journal article
- research article
- Published by Cambridge University Press (CUP) in The Journal of Laryngology & Otology
- Vol. 97 (3) , 223-226
- https://doi.org/10.1017/s0022215100094044
Abstract
Summary: Dematoplasty for the treatment of epistaxis caused by HHT has become well established. A modification of Saunders's (1960) original dermatoplastic technique is described, which permits the nasolabial incision to be avoided.This retrospective study of the long-term effect on epistaxis caused by HHT demonstrates, in contrast to those with a short period of observation, that epistaxis can be partially controlled by means of dermatoplasty and, further, that it is impossible to eliminate completely the need for blood transfusion.In two of the patients it was found that newly formed telangiectases had occurred in the transplant 15 and 18 years post-operatively.This publication has 4 references indexed in Scilit:
- Amniotic graft in the management of severe epistaxis due to hereditary haemorrhagic telangiectasiaThe Journal of Laryngology & Otology, 1979
- CLOSURE OF SEPTAL PERFORATION IN OSLER-WEBER-RENDUʼS DISEASE BY BILATERAL LABIAL-BUCCAL FLAPSPlastic and Reconstructive Surgery, 1978
- Management of Epistaxis in Hereditary Hemorrhagic Telangiectasia: Review of 80 CasesJAMA Otolaryngology–Head & Neck Surgery, 1977
- MANAGEMENT OF EPISTAXIS IN OSLERWEBER-RENDU DISEASEPlastic and Reconstructive Surgery, 1972