Unusual Presentation of Thoracic Epidural Ewing Sarcoma in a 20-Year-Old Patient: A Case Report.
Autor: | Markov D; General and Clinical Pathology, Medical University of Plovdiv, Plovdiv, BGR., Bechev KI; Neurological Surgery, University Multidisciplinary Hospital for Active Treatment (UMHAT) Pulmed, Plovdiv, BGR., Markov G; Medicine, Medical University of Plovdiv, Plovdiv, BGR., Hadzhieva SD; Neurology, University Hospital 'Pulmed', Plovdiv, BGR., Aleksiev V; Cardiovascular Surgery, Medical University of Plovdiv, Plovdiv, BGR., Poryazova EG; General and Clinical Pathology, Medical University of Plovdiv, Plovdiv, BGR. |
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Jazyk: | angličtina |
Zdroj: | Cureus [Cureus] 2024 Jun 22; Vol. 16 (6), pp. e62902. Date of Electronic Publication: 2024 Jun 22 (Print Publication: 2024). |
DOI: | 10.7759/cureus.62902 |
Abstrakt: | The aim of this case report is to present a rare case of epidural Ewing sarcoma with spinal cord compression, which is an uncommon presentation of this tumor. Ewing's sarcoma is a primary malignant tumor predominantly affecting individuals in their second decade of life, primarily impacting those aged 10 to 25, with the average age of onset being around 20 years. Epidemiological studies reveal that this cancer most commonly arises in the diaphyses of the long tubular bones in the lower extremities. Spinal involvement, however, is exceedingly uncommon. A case of sacral type of Ewing's sarcoma, with the most common localization of the primary spinal sarcomas and an extremely aggressive course, has been described in the literature. Other localizations of Ewing's sarcoma located in other areas of the spine are also presented. Even rarer are cases in which the tumor formation is located epidurally and exhibits marked medullary compression and absent neurological symptoms. We present the case of a 20-year-old patient who was admitted to the neurology department with symptoms of lower flaccid paraparesis and pelvic-reservoir dysfunction, specifically urinary retention for 16-17 hours, after which a catheter was added. MRI revealed an epidural tumor spanning TH5-TH7 vertebral levels, causing significant spinal cord compression. A CT scan of the chest identified a tumor on the left side at the level of the sixth rib, featuring soft tissue involvement, rib destruction, lung invasion, and a small pleural effusion. Due to the critical neurological symptoms, the patient underwent emergency surgery in the neurosurgical department, which included thoracic laminectomies, maximal possible tumor resection, and effective spinal cord decompression. Postoperative period was uneventful. Histopathological examination confirmed the diagnosis of Ewing's epidural sarcoma. The patient subsequently received adjuvant chemotherapy and radiotherapy. Six months post-treatment, the patient demonstrated a satisfactory overall condition with significant improvement in gait and continues to undergo chemotherapy courses. Competing Interests: Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work. (Copyright © 2024, Markov et al.) |
Databáze: | MEDLINE |
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