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肺癌相关性肥大性骨关节病:缺氧诱导因子-1α、血管内皮生长因子与过度血管化之间的可能联系。

Hypertrophic osteoarthropathy associated with lung cancer: Possible links among hypoxia-inducible factor-1α, vascular endothelial growth factor, and hypervascularization.

机构信息

Department of Respiratory Medicine, Sasebo City General Hospital, Nagasaki, Japan.

Department of Internal Medicine, Senju Hospital, Nagasaki, Japan.

出版信息

Thorac Cancer. 2023 May;14(14):1320-1324. doi: 10.1111/1759-7714.14869. Epub 2023 Mar 26.

DOI:10.1111/1759-7714.14869
PMID:36967655
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10175026/
Abstract

Hypertrophic osteoarthropathy (HOA) is a paraneoplastic syndrome, the exact pathogenesis of which remains to be elucidated. The case of a 69-year-old man who developed intractably painful HOA secondary to lung cancer is presented. Contrast-enhanced computed tomography of the chest showed an 80-mm solid nodule with a large low-density area. The patient was diagnosed as having stage IIIA undifferentiated non-small cell lung cancer. The combination of carboplatin and paclitaxel with bevacizumab reduced tumor size and plasma vascular endothelial growth factor (VEGF) levels, relieving his leg pain. On immunohistochemical examination, lung cancer cells were positive for VEGF. A hypoxic tumor microenvironment may have caused some lung cancer cells to express hypoxia-inducible factor-1α, which contributed, at least in part, to the production of VEGF. The deep dermis vessels showed proliferation in the shin, with their thickened walls positive for VEGF. These findings may encourage investigators to explore novel management strategies for painful HOA.

摘要

肥大性骨关节病(HOA)是一种副瘤综合征,其确切发病机制仍有待阐明。本文报告了一例 69 岁男性肺癌继发的难治性 HOA 病例。胸部增强 CT 显示 80mm 实性结节伴大片低密度区。患者被诊断为 IIIA 期未分化非小细胞肺癌。卡铂和紫杉醇联合贝伐珠单抗缩小了肿瘤大小并降低了血浆血管内皮生长因子(VEGF)水平,缓解了他的腿部疼痛。免疫组化检查显示肺癌细胞呈 VEGF 阳性。缺氧肿瘤微环境可能导致一些肺癌细胞表达低氧诱导因子-1α,这至少部分促成了 VEGF 的产生。小腿深部真皮血管显示增生,其增厚的血管壁呈 VEGF 阳性。这些发现可能鼓励研究人员探索治疗疼痛性 HOA 的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/ab3961518c4b/TCA-14-1320-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/ed7f378fc7a3/TCA-14-1320-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/7afdc5408a16/TCA-14-1320-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/8e5c50fbd9fd/TCA-14-1320-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/ab3961518c4b/TCA-14-1320-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/ed7f378fc7a3/TCA-14-1320-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/7afdc5408a16/TCA-14-1320-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/8e5c50fbd9fd/TCA-14-1320-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8337/10175026/ab3961518c4b/TCA-14-1320-g002.jpg

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