gms | German Medical Science

65. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

11. - 14. Mai 2014, Dresden

Atypical localization of grossly calcified Dysembryoplastic Neuroepithelial Tumor (DNET)

Meeting Abstract

  • Hakan Erdogan - Maltepe University School of Medicine, Department of Neurosurgery, Istanbul, Turkey
  • Bilal Kelten - Maltepe University School of Medicine, Department of Neurosurgery, Istanbul, Turkey
  • Seyho Cem Yucetas - Kafkas University School of Medicine, Department of Neurosurgery, Istanbul, Turkey
  • Veysel Antar - İstanbul Research and Training Hospital, Department of Neurosurgery, Istanbul, Turkey
  • Erol Tasdemiroglu - Institute of Neurological Sciences, Gelisim University, Istanbul, Turkey, Istanbul, Turkey

Deutsche Gesellschaft für Neurochirurgie. 65. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC). Dresden, 11.-14.05.2014. Düsseldorf: German Medical Science GMS Publishing House; 2014. DocP 036

doi: 10.3205/14dgnc431, urn:nbn:de:0183-14dgnc4313

Veröffentlicht: 13. Mai 2014

© 2014 Erdogan et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.de). Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.


Gliederung

Text

Objective: To report our experience with the case of grossly calcified Dysembryoplastic Neuroepithelial Tumor in Cerebellum (DNET)

Method: In our study we report a case of a 31-year-old male with headache and ataxia during the last six months. His neurological examination revealed no deficit. Magnetic resonance imaging with contrast enhancement showed well demarcated, heterogenously enhanced and disseminated signal void areas resembling hemorrhage with 35x45x56 mm dimensions of right cerebellar mass partially compressing to the brain stem. He underwent to limited craniectomy of posterior fossa and total removal of the tumor was accomplished by piece meal fashion. His postoperative period was uneventful and he was discharged from hospital on 10th day postoperatively. Histological examination showed small glial cells, oligodendrocytes-like, lying in an eosinophilic alveolar matrix with some floating neurons and extensive areas of calcification. His pathological report was Dysembryoplastic Neuroepithelial Tumor.

Results: Here we report an unusual case demonstrating that DNET may present as a totally calcified tumor of infratentorial localization.

Conclusions: DNET is a benign neoplasm of supratentorial region typically. Our case has unique findings because of the location and gross calcification of the tumor. Only four cases of cerebellar DNET and a few cases of DNETs that present gross calcification have been reported in the literature. To our knowledge, both findings in the same tumor have not been reported so far.