ACTA MEDICA, Vol 61 No 2 (2018), 60–64
From Ataxia to Diagnosis of Askin Tumor – a Case Report
Marko Bašković, Božidar Župančić, Mirko Žganjer, Igor Nikolić, Davor Ježek, Lucija Čizmić
DOI: https://doi.org/10.14712/18059694.2018.53
zveřejněno: 14. 09. 2018
Abstract
Peripheral primitive neuroectodermal tumors (pPNET) are a group of extremely rare, aggressive, malignant tumors that are most often found in the thorax (Askin tumor), abdomen, pelvis, extremities and less frequently in the head and neck. The most important prognostic factor is the stage of the tumor. Significant progress both in surgery and in neoadjuvant and adjuvant chemotherapy and radiotherapy, as well as the improvement in diagnosis by cytogenetic and immunohistochemical analysis, should improve the survival rate. We report a case of a 14-year-old girl, with ataxic gait, cardiopulmonary compensated, without respiratory symptoms, who was referred to our hospital for further examination and treatment of newly discovered tumor of the left hemithorax. After a detailed radiological and laboratory investigation, next step was an extensive thoraco-neurosurgical surgery. After histopathological, cytological and molecular analysis, a diagnosis of Askin tumor was made.
klíčová slova: Askin’s tumor; peripheral primitive neuroectodermal tumor; ataxia; pediatric surgery
From Ataxia to Diagnosis of Askin Tumor – a Case Report is licensed under a Creative Commons Attribution 4.0 International License.
210 x 297 mm
vychází: 4 x ročně
cena tištěného čísla: 150 Kč
ISSN: 1211-4286
E-ISSN: 1805-9694