Tracheal Chondrosarcoma: A Case Report and Discussion.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-09-23 eCollection Date: 2025-01-01 DOI:10.1159/000548086
Yordan Krastev, Rostislav Manev, Georgi Todorov, Nikolay Conev
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Abstract

Introduction: Tracheal chondrosarcoma is an exceedingly rare malignant tumor arising from the cartilage parts of the trachea, with less than 40 cases described in the English literature. We aim to explore the current literature on the topic and present 1 more case of tracheal chondrosarcoma in a 69-year-old male.

Case presentation: A 69-year-old male presented with upper airway obstruction and difficulty breathing. He also reported recent unintentional weight loss and night sweats. A computed tomography (CT) scan upon hospitalization revealed a large tumor formation that was obstructing the tracheal lumen and an interventional bronchoscopy for tumor debulking was performed. The histological examination determined it was a case of a high grade (G3) chondrosarcoma of the trachea. Later on, the patient underwent tracheal resection and reconstruction after which he was referred to radiation oncology for radiotherapy. Three months after concluding radiotherapy, a PET/CT scan showed no evidence of local recurrence or distant metastasis. On the fifth month post-radiation due to complaints of purulent discharge from the tracheostomy, a new biopsy was performed which determined there was local recurrence of the tumor. The patient was started on first-line chemotherapy with paclitaxel monotherapy. Restaging with CT scan was done after the fourth and sixth cycles, with inconclusive data for progression. Currently, he is scheduled to receive 4 more cycles' paclitaxel monotherapy and then be reevaluated.

Conclusion: The literature on the topic is still scarce and more cases reported are needed in order to optimize the treatment of our patients and achieve the best outcome.

气管软骨肉瘤1例报告及讨论。
气管软骨肉瘤是一种极为罕见的发生于气管软骨部分的恶性肿瘤,在英文文献中报道的病例不足40例。我们的目的是探讨当前文献的主题,并提出1例气管软骨肉瘤在一个69岁的男性。病例介绍:一名69岁男性,因上呼吸道阻塞及呼吸困难。他还报告说,最近体重意外减轻,还出现盗汗。住院时的计算机断层扫描(CT)显示一个大的肿瘤形成阻塞了气管腔,并进行了介入支气管镜检查以缩小肿瘤。组织学检查确定为气管高级别(G3)软骨肉瘤。后来,患者接受了气管切除术和重建,之后他被转介到放射肿瘤学进行放疗。放疗结束3个月后,PET/CT扫描未发现局部复发或远处转移的证据。放疗后第5个月,由于气管造口术后脓性分泌物的抱怨,进行了一次新的活检,确定肿瘤局部复发。患者开始一线化疗紫杉醇单药治疗。在第四个和第六个周期后进行CT扫描,没有确定的进展数据。目前,他计划再接受4个周期的紫杉醇单药治疗,然后重新评估。结论:关于该主题的文献仍然很少,需要更多的病例报道,以优化我们的患者的治疗方法,达到最佳效果。
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
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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