Chahla Elie, Cheesman Antonio, Hammami Muhammad, Taylor Jason R, Poddar Nishant, Garrett Robert W, Alkaade Samer
Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, Mo., USA.
Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, Mo., USA.
Case Rep Gastroenterol. 2015 Feb 10;9(1):44-8. doi: 10.1159/000376608. eCollection 2015 Jan-Apr.
Acute esophagitis and esophageal strictures typically occur after local radiation therapy to the thoracic field. Toxicity is usually limited to the field of radiation and potentially augmented by concomitant use of chemotherapy, however esophageal stricturing due to chemotherapy alone is exceedingly rare. Gastrointestinal toxicity has been previously reported in the setting of 5-fluorouracil (5-FU)-based chemotherapy with abnormal thymidylate synthase or dihydropyrimidine dehydrogenase activities. We present a unique case of isolated chemotherapy-induced esophageal stricture in the setting of stage IIIa rectal adenocarcinoma which presented shortly after initiation of treatment with 5-FU-based chemotherapy in a patient with normal thymidylate synthase and dihydropyrimidine dehydrogenase assays. These findings prompt further investigation of pathways and potential risk factors leading to esophageal toxicity in patients treated with 5-FU-based chemotherapy.
急性食管炎和食管狭窄通常发生在胸部区域接受局部放射治疗之后。毒性通常局限于放射野,同时使用化疗可能会加重毒性,然而,单纯化疗导致的食管狭窄极为罕见。先前曾有报道,在基于5-氟尿嘧啶(5-FU)的化疗中,由于胸苷酸合成酶或二氢嘧啶脱氢酶活性异常而出现胃肠道毒性。我们报告了一例独特的病例,一名IIIa期直肠腺癌患者在开始基于5-FU的化疗后不久出现了孤立的化疗诱导食管狭窄,该患者的胸苷酸合成酶和二氢嘧啶脱氢酶检测结果正常。这些发现促使人们进一步研究在接受基于5-FU化疗的患者中导致食管毒性的途径和潜在风险因素。