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隆突性皮肤纤维肉瘤肺转移灶的手术切除

Surgical Excision of Pulmonary Metastases of Dermatofibrosarcoma Protuberans.

作者信息

Nocera Adriana, Zhang Qianqian, Napolitano Antonio Giulio, Nachira Dania, Petracca-Ciavarella Leonardo, Congedo Maria Teresa, Cancellieri Alessandra, Schinzari Giovanni, Peris Ketty, Margaritora Stefano, Meacci Elisa

机构信息

Thoracic Surgery, Fondazione Policlinico Universitario "Agostino Gemelli" IRCCS, Università Cattolica del Sacro Cuore, Roma, ITA.

Anatomic Pathology, Fondazione Policlinico Universitario "Agostino Gemelli" IRCCS, Università Cattolica del Sacro Cuore, Roma, ITA.

出版信息

Cureus. 2024 Oct 8;16(10):e71076. doi: 10.7759/cureus.71076. eCollection 2024 Oct.

Abstract

Dermatofibrosarcoma protuberans (DFSP) is a rare malignancy of mesenchymal origin of medium-low grade with a tendency to local recurrences but not to distant metastases. We present the case of a 37-year-old male who underwent surgical resection of a 1.2 cm DFSP lesion on the left shoulder in May 2020. In the absence of a standardized follow-up protocol for DFSP, the attending physician opted for ultrasound monitoring every six months to detect any local recurrences. Due to chest pain and mild exertional dyspnea, a CT scan was performed three years post-excision revealed a 10 cm mass in the left lower lung lobe and two lesions in the right lung measuring 3.2 cm and 1.2 cm, respectively. Thoracotomy was performed in July 2023 to remove the large lesion in the left lower lobe, necessitating intrapericardial resection of the left lower pulmonary vein and extra-pleural dissection due to parietal pleural infiltration. Uniportal-video-assisted thoracoscopic surgery (U-VATS) was performed one month later to resect the lesions on the right side. Pathological examination showed high mitotic activity, cellularity, and nuclear pleomorphism, in the absence of other malignant mesenchymal neoplasms, suggesting fibrosarcomatous transformation of DFSP in the metastatic lesions (FS-DFSP). The patient remains disease-free under close radiological and clinical surveillance. Given the potential for aggressive transformation and the risk of recurrence and distant metastasis, our experience suggests including chest CT scans in the follow-up algorithms for DFSP.

摘要

隆突性皮肤纤维肉瘤(DFSP)是一种罕见的中低级别间叶源性恶性肿瘤,有局部复发倾向,但无远处转移倾向。我们报告一例37岁男性病例,该患者于2020年5月接受了左肩部1.2 cm DFSP病变的手术切除。由于缺乏DFSP的标准化随访方案,主治医师选择每六个月进行一次超声监测以发现任何局部复发情况。三年后,由于胸痛和轻度劳力性呼吸困难,患者进行了CT扫描,结果显示左下肺叶有一个10 cm的肿块,右肺有两个分别为3.2 cm和1.2 cm的病灶。2023年7月进行了开胸手术以切除左下叶的大病灶,由于壁层胸膜浸润,需要进行左下肺静脉的心包内切除和胸膜外剥离。一个月后进行了单孔电视辅助胸腔镜手术(U-VATS)以切除右侧的病灶。病理检查显示有高有丝分裂活性、细胞密度和核多形性,且无其他恶性间叶性肿瘤,提示转移病灶中DFSP发生了纤维肉瘤样转化(FS-DFSP)。在严密的影像学和临床监测下,患者目前无疾病复发。鉴于存在侵袭性转化的可能性以及复发和远处转移的风险,我们的经验表明在DFSP的随访方案中应包括胸部CT扫描。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d5/11542332/c5ac5d6ccc1a/cureus-0016-00000071076-i01.jpg

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