Late Lung Metastasis in a Patient with a Clear Cell Chondrosarcoma: An Indication for a Life-Long Follow-Up?

IF 0.6 Q4 ONCOLOGY
Case Reports in Oncological Medicine Pub Date : 2021-12-02 eCollection Date: 2021-01-01 DOI:10.1155/2021/7205649
Paulien West, Celine Jacobs, Michael Saerens, David Creytens, Gwen Sys, Lore Lapeire
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引用次数: 0

Abstract

Background: Clear cell chondrosarcoma (CCCS) is a rare subtype of chondrosarcoma and comprises between 1.6% and 2.5% of all chondrosarcoma. They are known to be chemo- and radiotherapy resistant; surgical resection is therefore the therapy of choice.

Methods: We present a 63-year-old woman with a progressive lung nodule 20 years after initial diagnosis and treatment of a clear cell chondrosarcoma of the right os naviculare.

Results: On serial CT scans of the chest, an asymptomatic, slowly growing nodule in the left upper lung lobe was detected. CT-guided transthoracic biopsy of this nodule confirmed the diagnosis of a chondrosarcoma lung metastasis. Video-assisted thoracoscopic wedge resection was performed with complete removal of the nodule. The patient recovered well from surgery and remains in good health during further follow-up.

Conclusion: Given the tendency of clear cell chondrosarcoma to recur and metastasize after extended periods of time, a long-term, possibly life-long follow-up and clinical surveillance is advisable in these patients.

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透明细胞软骨肉瘤晚期肺转移:终身随访的指征?
背景:透明细胞软骨肉瘤(CCCS)是一种罕见的软骨肉瘤亚型,占所有软骨肉瘤的1.6% - 2.5%。已知它们具有化疗和放疗抗性;因此,手术切除是首选的治疗方法。方法:我们报告一名63岁的女性,在最初诊断和治疗20年后,出现了一个进行性肺结节右脐透明细胞软骨肉瘤。结果:胸部连续CT扫描,发现左侧肺上叶无症状,缓慢生长的结节。ct引导下经胸活检证实结节为软骨肉瘤肺转移。视频辅助胸腔镜楔形切除,完全切除结节。患者术后恢复良好,在进一步随访期间健康状况良好。结论:考虑到透明细胞软骨肉瘤在较长时间后复发和转移的趋势,建议对这些患者进行长期的,可能是终身的随访和临床监测。
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来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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