Guzel, A.Tatli, M.Belen, D.Seckin, H.2024-04-242024-04-2420071362-43931476-5624https://doi.org/10.1038/sj.sc.3101942https://hdl.handle.net/11468/16460Study design: Case report. Objective: To report an adult male patient witha primary extragonadal giant yolk sac tumor presenting with acute spinal cord compression. Setting: Faculty of Medicine, University of Dicle, Diyarbakir, Turkey. Method: A 31-year-old man was referred to our department witha diagnosis of Pott's disease, a complaint of back pain and gait difficulty for 2 weeks. Neurological examination showed spastic paraparesis and hypoesthesia below the L2 dermatome level. He also had urinary incontinence. Abdominal computed tomography and lumbar magnetic resonance imaging study revealed a giant cystic mass lesion located in the psoas muscle. Posteriorly, the third lumbar vertebral body was destructed and the tumor was compressing the dural sac. A combined anterior and posterior approach was performed. Pathological diagnosis was a yolk sac tumor. Result: His neurological status improved during the postoperative course. A chemotherapy protocol was given including bleomycin, etoposide and cisplatin. Five months after the last chemotherapy, he was brought to the emergency unit in sepsis and died despite antibiotherapy. Conclusion: Yolk sac tumor should be considered in young adult male patients presenting with acute paraparesis even without any signs or medical history of a testis tumor. These tumors may be unresectable; however, decompression of neural structures and stabilization of the spine with instrumentation may cause substantial improvement in neurological deficit and pain relief.eninfo:eu-repo/semantics/openAccessAdultLumbar ColumnParaparesisPrimary Yolk Sac TumorSpinal cord compression of primary extragonadal giant yolk sac tumorSpinal cord compression of primary extragonadal giant yolk sac tumorArticle453254257WOS:0002445708000082-s2.0-338473707291673351910.1038/sj.sc.3101942Q1Q3