吉西他滨致肺动脉高压1例。

Janice Shen, Su Yun Chung, Elham Azimi-Nekoo, Jyothi Jose, Muhammad W Saif
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引用次数: 0

摘要

背景:吉西他滨是局部晚期和转移性肝内胆管癌全身治疗的支柱。在最近的文献中,吉西他滨与各种肺部副作用有关。病例报告:我们报告了一例82岁的男性在接受一个周期的吉西他滨治疗转移性胆管癌后发生急性肺动脉高压。他的症状开始是疲劳,呼吸急促和咳嗽,尽管剂量减少,但病情恶化。新发双侧肺积液,超声心动图显示肺动脉高压。计算机断层扫描(CT)血管造影为肺血栓栓塞阴性。尽管他及时接受了利尿剂和类固醇治疗,但病人无法忍受任何进一步的治疗。结论:吉西他滨引起的肺动脉高压是罕见的,诊断具有挑战性,因为它仍然是一种排除性的诊断。然而,医生应该警惕新的肺部症状,因为延迟治疗可能导致显著的患者发病率和死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Rare Case of Gemcitabine-Induced Pulmonary Hypertension.

Context: Gemcitabine is the backbone of systemic treatment of locally advanced and metastatic intrahepatic cholangiocarcinoma. In recent literature, gemcitabine has been linked to various pulmonary side effects.

Case report: We report a case of an 82-year-old male who developed acute pulmonary hypertension after receiving one cycle of gemcitabine for metastatic cholangiocarcinoma. His symptoms began with fatigue associated with shortness of breath and cough that worsened despite dose reduction. He developed new onset bilateral pulmonary effusions and an echocardiogram revealed findings consistent with pulmonary hypertension. A computed tomography (CT) angiogram was negative for pulmonary thromboembolism. Although he was promptly treated with diuretics and steroids, the patient could not tolerate any further therapy.

Conclusion: Gemcitabine-induced pulmonary hypertension is rare and can be challenging to diagnose, as it remains a diagnosis of exclusion. However, physicians should be vigilant of new pulmonary symptoms, as delayed treatment can cause significant patient morbidity and mortality.

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A Rare Case of Gemcitabine-Induced Pulmonary Hypertension.
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