Sudhir G, Jayabalan S Vignesh, Ram Amith, Gadde Saikrishna, Kailash Karthik
Department of Spine Surgery, Sri Ramachandra Institute of Higher Education and Research, Porur, Chennai, Tamil Nadu, India.
Asian J Neurosurg. 2021 Feb 23;16(1):191-195. doi: 10.4103/ajns.AJNS_190_20. eCollection 2021 Jan-Mar.
Epithelioid sarcoma of the spine has been rarely reported in the literature. Its diagnosis is challenging due to nonspecific findings. We report a case of 42-year-old gentleman with back pain. Magnetic resonance imaging (MRI) revealed lesion in the L4 vertebral body extending into the spinal canal with pre and paravertebral involvement. He underwent posterior spinal decompression and instrumentation with biopsy. Histopathological examination was nonspecific. Considering clinical and radiological features, antitubercular treatment was initiated. The patient developed acute onset weakness of both lower extremities 1 month post-surgery. Repeat MRI and positron emission tomography (PET) computed tomography revealed an increase in the extent of lesion which required revision decompression. Histopathological examination showed cells with epithelioid appearance, positive for Vimentin, and epitheloid membrane antigen in immunohistochemistry. Radiotherapy was planned but the patient expired due to multiorgan dysfunction. Epithelioid sarcomas are rare soft-tissue neoplasms with poor prognosis. They can mimic infection and a high degree of suspicion is required in these cases to diagnose and treat them early.
脊柱上皮样肉瘤在文献中鲜有报道。因其表现不具特异性,故诊断颇具挑战性。我们报告一例42岁男性背痛患者。磁共振成像(MRI)显示L4椎体有病变,延伸至椎管,伴有椎前和椎旁受累。他接受了后路脊柱减压及内固定并活检。组织病理学检查结果不具特异性。综合临床和放射学特征,开始进行抗结核治疗。患者术后1个月出现双下肢急性无力。复查MRI及正电子发射断层扫描(PET)计算机断层扫描显示病变范围增大,需再次减压。组织病理学检查显示细胞呈上皮样外观,波形蛋白及上皮细胞膜抗原免疫组化呈阳性。计划进行放疗,但患者因多器官功能障碍死亡。上皮样肉瘤是罕见的软组织肿瘤,预后较差。它们可酷似感染,对此类病例需高度怀疑,以便早期诊断和治疗。