CC BY-NC-ND 4.0 · J Neurol Surg Rep 2018; 79(04): e79-e82
DOI: 10.1055/s-0038-1673626
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Giant Calvarial Ewing's Sarcoma: A Case Report

Buse Sarigul
1   Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey
,
Ece Uysal
1   Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey
,
İdris Avci
1   Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey
,
Halil Peker
1   Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey
,
Suat Celik
1   Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey
› Institutsangaben
Weitere Informationen

Publikationsverlauf

17. April 2018

28. August 2018

Publikationsdatum:
05. Oktober 2018 (online)

Abstract

Ewing's sarcoma (EWS) is the second most common primary bone tumor seen in children and adolescents, first being osteosarcoma. Skull lesions are seen in 6 to 9% of cases. The tumor tends to reside most frequently on frontal and parietal bones. In the literature, majority of papers on calvarial EWS present cases with intracranial involvement; extracranial extension is reported in only eight cases. The case that we are presenting in this report is a 23-year-old male patient with multiple infiltrations in femur, costal bones, and calvarium which had been diagnosed radiologically and histopathologically as EWS. The calvarial metastasis had reached a very huge size with dimensions of approximately 7.5 × 7.5 × 9.5 cm and was successfully excised totally. Twelve months of follow-up revealed no recurrence in the surgical site showing that total removal of giant cranial EWS may improve morbidity of these patients.

 
  • References

  • 1 Choi EY, Gardner JM, Lucas DR, McHugh JB, Patel RM. Ewing sarcoma. Semin Diagn Pathol 2014; 31 (01) 39-47
  • 2 Balamuth NJ, Womer RB. Ewing's sarcoma. Lancet Oncol 2010; 11 (02) 184-192
  • 3 Cherekaev VA, Kushel' IuV, Shkarubo AN. , et al. [Primary and metastatic Ewing sarcoma of the skull base - case reports and comparative analysis]. Vopr Neirokhir 2013; 77 (01) 30-36 , discussion 36
  • 4 Kawano H, Nitta N, Ishida M, Fukami T, Nozaki K. Primary pericranial Ewing's sarcoma on the temporal bone: a case report. Surg Neurol Int 2016; 7 (Suppl, 15): S444 –S448
  • 5 Sujan MU, Rao MR, Kisan R. , et al. Influence of hydrotherapy on clinical and cardiac autonomic function in migraine patients. J Neurosci Rural Pract 2016; 7 (01) 109-113
  • 6 Salunke P, Sharma M, Gupta K. Ewing sarcoma of the occipital bone in an elderly patient. World Neurosurg 2014; 81 (02) e10 –e12
  • 7 Winn HR. Youmans & Winn Neurological Surgery. 7th ed. New York, NY: Elsevier; 2016. :1322–1343
  • 8 Pfeiffer J, Boedeker CC, Ridder GJ. Primary Ewing sarcoma of the petrous temporal bone: an exceptional cause of facial palsy and deafness in a nursling. Head Neck 2006; 28 (10) 955-959
  • 9 Jing Z, Wen-Yi L, Jian-Li L, Jun-Lin Z, Chi D. The imaging features of meningeal Ewing sarcoma/peripheral primitive neuroectodermal tumours (pPNETs). Br J Radiol 2014; 87 (1041); 20130631
  • 10 Güzel A, Tatli M, Er U, Yilmaz F, Bavbek M. Multifocal Ewing's sarcoma of the brain, calvarium, leptomeninges, spine and other bones in a child. J Clin Neurosci 2008; 15 (07) 813-817
  • 11 Mardekian SK, Gandhe A, Miettinen M, Pack S, Curtis MT, Abdullaev Z. Two cases of spinal, extraosseous, intradural Ewing's sarcoma/peripheral neuroectodermal tumor: radiologic, pathologic, and molecular analysis. J Clin Imaging Sci 2014; 4: 6