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伴有4年乳腺癌病史的原发性肺去分化软骨肉瘤:一例报告

Primary dedifferentiated chondrosarcoma of the lung with a 4-year history of breast cancer: A case report.

作者信息

Wen Huan, Gong Feng-Jie, Xi Jian-Min

机构信息

Department of Pathology, Hunan Provincial Hospital of Integrated Traditional Chinese and Western Medicine, Changsha 410006, Hunan Province, China.

Department of Radiology, Hunan Provincial Hospital of Integrated Traditional Chinese and Western Medicine, Changsha 410006, Hunan Province, China.

出版信息

World J Clin Cases. 2023 May 6;11(13):3022-3028. doi: 10.12998/wjcc.v11.i13.3022.

Abstract

BACKGROUND

Primary dedifferentiated chondrosarcoma (DDCS) of the lung is extremely rare and has a poor prognosis, especially in patients with a history of carcinomas and related treatment. Herein, we report a case of primary DDCS of the lung in a patient with a 4-year history of breast cancer and related treatment.

CASE SUMMARY

A 49-year-old woman was admitted to our hospital with complaints of headache, dizziness, slurred speech, and dyskinesia in May 2021. Computed tomography (CT) examinations showed multiple nodules in the brain, vertebral body, and both lungs with multiple enlarged lymph nodes in the right hilum and mediastinum, which were considered metastases of breast cancer. No obvious mass was discovered in the right hilum. After several months of related administration, the patient's headache disappeared, and her condition improved. However, new problems of asthma, dyspnea, cough, and restricted activity appeared in late November 2021. Although the CT scan indicated that the lesions in the brain, lung, and vertebral body had shrunk or disappeared, a soft tissue density lesion appeared in her right hilum and blocked the bronchial lumen. To relieve her dyspnea, part of the mass was resected, and a stent was placed fiberoptic bronchoscopy. Following a complete pathological examination of the tumor, it was confirmed to be a primary DDCS of the lung. The patient then received two rounds of systemic chemotherapy with a regimen of cisplatin + ifosfamide + doxorubicin hydrochloride liposome, palliative radiotherapy for the tumor in her right lung, and four cycles of systemic chemotherapy and targeted therapy with a regimen of temozolomide combined with bevacizumab successively. She was in stable condition after the completion of the systemic chemotherapy and targeted therapy but underwent rapid progression after lung radiotherapy. The CT examinations showed multiple nodules in the brain and in both lungs, and the tumor in the right hilum was increased in size.

CONCLUSION

This case revealed a rare primary DDCS of the lung with a medical history of breast cancer, meaning a worse prognosis and making it more difficult to treat.

摘要

背景

原发性肺去分化软骨肉瘤(DDCS)极为罕见,预后较差,尤其是有癌症病史及相关治疗史的患者。在此,我们报告一例有4年乳腺癌病史及相关治疗史的原发性肺DDCS患者。

病例摘要

一名49岁女性于2021年5月因头痛、头晕、言语不清和运动障碍入院。计算机断层扫描(CT)检查显示脑、椎体及双肺有多个结节,右肺门和纵隔有多个肿大淋巴结,考虑为乳腺癌转移。右肺门未发现明显肿块。经过数月的相关治疗,患者头痛消失,病情好转。然而,2021年11月下旬出现了哮喘、呼吸困难、咳嗽和活动受限等新问题。尽管CT扫描显示脑、肺和椎体的病变已缩小或消失,但右肺门出现了一个软组织密度病变并阻塞了支气管腔。为缓解其呼吸困难,切除了部分肿块,并通过纤维支气管镜置入了支架。对肿瘤进行全面病理检查后,确诊为原发性肺DDCS。随后患者接受了两轮顺铂+异环磷酰胺+盐酸阿霉素脂质体方案的全身化疗、右肺肿瘤姑息性放疗,以及先后四个周期的替莫唑胺联合贝伐单抗方案的全身化疗和靶向治疗。完成全身化疗和靶向治疗后病情稳定,但肺部放疗后病情迅速进展。CT检查显示脑和双肺有多个结节,右肺门肿瘤增大。

结论

该病例显示了一例罕见的有乳腺癌病史的原发性肺DDCS,预后较差且治疗难度更大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90ac/10198077/b56852c89f17/WJCC-11-3022-g001.jpg

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