Miguel Isabel R, Arantes Mavilde, Matias Rafael, Ferreira Ana M, Afonso Mariana
Radiation Oncology, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, PRT.
Neuroradiology, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, PRT.
Cureus. 2024 Dec 11;16(12):e75544. doi: 10.7759/cureus.75544. eCollection 2024 Dec.
Sclerosing epithelioid fibrosarcoma (SEF) is a rare and aggressive neoplasm composed of epithelioid cells arranged in strands and nests embedded in a highly sclerotic collagenous stroma. We report a case of a 36-year-old man who started with lumbar pain, with extension to both legs, night sweats, and weight loss. He underwent magnetic resonance imaging (MRI) of the lumbar spine; computed tomography (CT) scan of the chest, abdomen, and pelvis; and [18F]-fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT) scan. The CT scan revealed a 13 cm thoracic mass, the MRI presented with diffuse neoplastic invasion of the vertebrae, and the PET showed hepatic, bone, and possibly pulmonary metastases. The histological diagnosis was compatible with SEF. The disease progressed very quickly, namely, with an episode of spinal cord compression, which made the patient paraplegic. He underwent surgery and, subsequently, radiotherapy (RT). Due to the clinical and analytical evolution, it was not possible to initiate systemic treatment and the patient ultimately passed away. In conclusion, SEF is an aggressive type of sarcoma that affects middle-aged patients, with high rates of distant metastases and mortality. The usual treatment is surgery followed by either radiotherapy or chemotherapy. However, further clinical trials are needed to find more systemic target therapies.
硬化性上皮样纤维肉瘤(SEF)是一种罕见的侵袭性肿瘤,由上皮样细胞组成,这些细胞排列成束状和巢状,包埋于高度硬化的胶原性间质中。我们报告一例36岁男性患者,最初表现为腰痛,并放射至双下肢,伴有盗汗和体重减轻。他接受了腰椎磁共振成像(MRI)、胸部、腹部和骨盆的计算机断层扫描(CT)以及[18F] - 氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(18F - FDG PET/CT)检查。CT扫描显示一个13厘米的胸部肿块,MRI显示椎体弥漫性肿瘤浸润,PET显示肝脏、骨骼及可能的肺部转移。组织学诊断符合SEF。疾病进展非常迅速,出现了一次脊髓压迫事件,导致患者截瘫。他接受了手术,随后进行了放疗(RT)。由于临床和分析结果的演变,无法开始全身治疗,患者最终死亡。总之,SEF是一种侵袭性肉瘤,影响中年患者,远处转移率和死亡率高。通常的治疗方法是手术,随后进行放疗或化疗。然而,需要进一步的临床试验来寻找更多的全身靶向治疗方法。