乳腺癌放疗和来曲唑后闭塞性细支气管炎组织肺炎1例并文献复习

Alati Aurélia, C. Pierre, Leobon Sophie
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摘要

目的:闭塞性细支气管炎组性肺炎在乳房保守治疗后发生率为1-3%。对于肺部或周围组织的辐射,炎症反应可影响双肺,并位于辐射场内。特征性影像学表现为多发肺泡浊影和弥漫性磨玻璃影。来曲唑可诱发医源性组织性肺炎。材料与方法:我们报告一位76岁女性因左乳浸润性导管癌接受保守治疗的病例。采用三维放射技术,分16次放疗,总剂量为42.5 Gy,总剂量为2.65 Gy。放疗结束后改用来曲唑。结果:放疗结束几周后,患者开始使用来曲唑,出现流感样症状。样本呈阴性,四疗程抗生素治疗后无改善。影像学提示闭塞性细支气管炎组织性肺炎。停用来曲唑后症状减轻,放疗结束11个月后影像学结果清晰。结论:医生必须考虑闭塞性细支气管炎组织性肺炎。随着低分割放疗和新药物的使用,病例可能增加。来曲唑可能会增加风险。剂量测定法可适用于有危险因素和服用辅助或同时服用有潜在肺毒性药物的患者的肺和胸膜下区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bronchiolitis Obliterans Organizing Pneumonia after Breast Cancer Radiotherapy and letrozole: A Case Report and Literature Review
Objectives: Bronchiolitis obliterans organizing pneumonia occurs with prevalence rate 1–3% after breast conservative treatment in series. In response to radiation of a lung or surrounding tissues, an inflammatory reaction can affect both lungs and is located within the radiation field. Characteristic imaging features include multiple alveolar opacities and diffuse ground-glass shadows. Letrozole may induce iatrogenic organizing pneumonia. Materials and methods: we report the case of a 76-year-old female who underwent conservative treatment for an invasive ductal carcinoma of the left breast. Hypofractionated radiotherapy was delivered with a total dose of 42.5 Gy in 16 sessions of 2.65 Gy using a three-dimensional technique. After the radiotherapy ended letrozole was indicated. Results: Several weeks after the radiotherapy ended and letrozole was introduced, she described a flu-like syndrome. Samples were negative, and there was no improvement after four courses of antibiotics. Imaging suggested bronchiolitis obliterans organizing pneumonia. Her symptomatology lessened after the letrozole was discontinued, and 11 months after radiotherapy finished, her imaging results were clear. Conclusion: Physicians must consider bronchiolitis obliterans organizing pneumonia. Cases may increase with hypofractionated radiation treatment and new drugs. Letrozole may potentiate the risk. Dosimetry may be adapted to the lung and subpleural areas for patients with risk factors and taking adjuvant or concurrent drugs with potential pneumotoxicity.
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