A case of malignant phyllodes tumor that responded to pazopanib and developed pneumothorax.

IF 0.5 Q4 ONCOLOGY
Hirofumi Ohmura, Takaaki Masuda, Koshi Mimori, Eishi Baba, Takahiko Horiuchi
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引用次数: 1

Abstract

Here, we present a 59-year-old female with recurrent malignant phyllodes tumor with multiple lung and lymph node metastases who developed a pneumothorax after the administration of pazopanib. The patient received pazopanib as the second-line chemotherapy. After 2.5 months of the therapy, computed tomography (CT) showed a decrease in the sizes and cavitation of lung lesions; however, a left pneumothorax was newly observed. It was difficult to distinguish the pneumothorax by upright chest X-ray. Typical symptom or physical finding of pneumothorax, such as dyspnea, chest pain or decreased breath sound was not observed. As the pneumothorax was small and asymptomatic, the administration of pazopanib was discontinued and follow-up chest X-ray and CT were performed. After 1 week, CT showed an improvement in the pneumothorax. Chemotherapy was switched to eribulin; however, a rapid increase in sizes of lung lesions was observed after the first administration of eribulin, pazopanib was reintroduced. Careful follow-up by chest X-ray and CT was performed and the pneumothorax has not recurred.

恶性叶状瘤对帕唑帕尼有效并发气胸1例。
在此,我们报告一位59岁的女性复发性叶状恶性肿瘤伴多发肺和淋巴结转移,在给予帕唑帕尼后发生气胸。患者接受帕唑帕尼作为二线化疗。治疗2.5个月后,计算机断层扫描(CT)显示肺病变大小和空化减小;然而,新发现左侧气胸。直立胸片很难鉴别气胸。未见气胸的典型症状或体征,如呼吸困难、胸痛或呼吸音减弱。因气胸小且无症状,停用帕唑帕尼,随访胸部x线及CT。1周后,CT显示气胸好转。化疗改为艾瑞布林;然而,在第一次给药后,观察到肺部病变的大小迅速增加,再次引入帕唑帕尼。经胸部x线及CT仔细随访,气胸未复发。
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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来源期刊
自引率
14.30%
发文量
57
期刊介绍: This online-only journal publishes original case reports on all types of cancer. In particular, we welcome not only case reports of educational value in the diagnosis and treatment of cancers, but also reports on molecularly analyzed cancer cases, including gene mutations, gene fusions, gene expression, and changes in copy number, regardless of their known clinical significance. Assessing the molecular analysis of a tumor usually requires a “cancer conference” in which experts from various fields discuss it. Even if the authors and their respective “cancer conference” were unable to determine the clinical significance of molecular changes at the time of submission and publication, their data may provide evidence that will help the scientific community develop precision medicine solutions in the future. We welcome case reports with reviews of the literature on similar cases, as they are more useful and valuable to readers than are reports of rare cases. International Cancer Conference Journal is the official publication of the Japan Society of Clinical Oncology (JSCO). - Presents an online-only collection of original case reports on all types of cancer - In particular, welcomes molecularly analyzed cancer cases - The Official Publication of the Japan Society of Clinical Oncology (JSCO)
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