Severe colitis after administration of UFT chemotherapy for temporal bone carcinoma
dc.contributor.author | Akay S. | |
dc.contributor.author | Özütemiz Ö. | |
dc.contributor.author | Doganavsargil B. | |
dc.date.accessioned | 2019-10-27T00:22:40Z | |
dc.date.available | 2019-10-27T00:22:40Z | |
dc.date.issued | 2004 | |
dc.department | Ege Üniversitesi | en_US |
dc.description.abstract | UFT (Uftoral®), a blend of uracil and Tegafur, is an antitumour agent for oral administration that is presumed to maintain the concentration of 5-fluorouracil (5-FU) in tumour tissue. As a result of increased use of high-dose 5-FU-based chemotherapy for various solid tumours, complicated drug-induced colitis is more frequently observed. Dihydropyrimidine dehydrogenase (DPD) is the rate-limiting enzyme in the catabolism of 5-FU and its deficiency is responsible for the severe toxicities encountered in cancer patients receiving 5-FU. The authors present the case of a patient with locally advanced temporal bone carcinoma who developed haematochezia during a course of chemotherapy with UFT. Colonoscopy of the patient showed bleeding petechia-like lesions and superficial inflammatory exudate, whilst histology revealed non-specific inflammatory changes of the colon mucosa. As the haematochezia improved with supportive treatment, neutropenia complicated the clinical picture. This patient developed life-threatening UFT toxicity without an exon-14 DPD gene mutation. 2004 © Ashley Publications Ltd. | en_US |
dc.identifier.doi | 10.1517/14740338.3.2.89 | en_US |
dc.identifier.endpage | 92 | en_US |
dc.identifier.issn | 1474-0338 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.pmid | 15006714 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 89 | en_US |
dc.identifier.uri | https://doi.org/10.1517/14740338.3.2.89 | |
dc.identifier.uri | https://hdl.handle.net/11454/22627 | |
dc.identifier.volume | 3 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Expert Opinion on Drug Safety | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Colitis | en_US |
dc.subject | Dihydropyrimidine dehydrogenase (DPD) deficiency | en_US |
dc.subject | Gastrointestinal (GI) side effects | en_US |
dc.subject | UFT | en_US |
dc.title | Severe colitis after administration of UFT chemotherapy for temporal bone carcinoma | en_US |
dc.type | Article | en_US |