Pediatric Patient with a Diagnosis of Pelvic Extraosseous Ewing's Sarcoma: A Case Report.
| Autor: | Amaouche S; Uz Brussel, Belgium., Devalck C; Universitair Kinderziekenhuis Koningin Fabiola, Belgium., Damry N; Universitair Kinderziekenhuis Koningin Fabiola, CHU Brugmann, Belgium. |
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| Jazyk: | angličtina |
| Zdroj: | Journal of the Belgian Society of Radiology [J Belg Soc Radiol] 2023 Sep 07; Vol. 107 (1), pp. 72. Date of Electronic Publication: 2023 Sep 07 (Print Publication: 2023). |
| DOI: | 10.5334/jbsr.3249 |
| Abstrakt: | Ewing's sarcoma (ES) is a malignant tumor that arises mainly from bone tissue. Primary extraosseous Ewing sarcoma (EES) is a rare form of the Ewing's sarcoma family of tumor, and pelvic localization is even more unusual, considered to be one of the rarest localizations [1]. We present the case of a seven-year-old boy with persistent abdominal pain. Ultrasound (US), contrast-enhanced computed tomography (CECT), and magnetic resonance imaging (MRI) revealed the presence of a large, solid, and heterogeneous mass in the pelvis. The histological and immunohistochemistry were compatible with pelvic EES. Teaching point: Extraosseous Ewing's sarcoma is a rare pediatric tumoral entity that requires clinician and radiological vigilance and detection. Competing Interests: The authors have no competing interests to declare. (Copyright: © 2023 The Author(s).) |
| Databáze: | MEDLINE |
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