A 36-year-old man with fourth ventricular mass.

NeuropathologyVolume 36, Issue 5 p. 504-507 NEUROPATHOLOGY EDUCATION A 36-year-old man with fourth ventricular mass Kongsak Loharamtaweethong, Corresponding Author Kongsak Loharamtaweethong Department of Anatomical Pathology, Navamindradhiraj University, Bangkok, ThailandCorrespondence: K. Loharamtaweethong, MD, Department of Anatomical Pathology, Faculty of Medicine, Vajira Hospital, Navamindradhiraj University, 681 Samsen Road, Dusit, Bangkok, 10300 Thailand. Email: [email protected]Search for more papers by this authorApisada Sutepvarnon, Apisada Sutepvarnon Department of Medical Oncology, Faculty of Medicine, Vajira Hospital, Navamindradhiraj University, Bangkok, ThailandSearch for more papers by this author Kongsak Loharamtaweethong, Corresponding Author Kongsak Loharamtaweethong Department of Anatomical Pathology, Navamindradhiraj University, Bangkok, ThailandCorrespondence: K. Loharamtaweethong, MD, Department of Anatomical Pathology, Faculty of Medicine, Vajira Hospital, Navamindradhiraj University, 681 Samsen Road, Dusit, Bangkok, 10300 Thailand. Email: [email protected]Search for more papers by this authorApisada Sutepvarnon, Apisada Sutepvarnon Department of Medical Oncology, Faculty of Medicine, Vajira Hospital, Navamindradhiraj University, Bangkok, ThailandSearch for more papers by this author First published: 18 November 2015 https://doi.org/10.1111/neup.12279Citations: 1Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1Ewing J. Diffuse endothelioma of bone. Proc N Y Pathol Soc 1921; 21: 17–24. 2Ahmad R, Mayol B, Davis M et al. Extraskeletal Ewing's sarcoma. Cancer 1999; 85: 725–731. 3Stechschulte SU, Kepes JJ, Holladay FP, McKittrick RJ. Primary meningeal extraosseous Ewing's sarcoma: case report. Neurosurgery 1994; 35: 143–147. 4dos Santos Rubio EJ, Harhangi BS, Kros JM, Vincent AJ, Dirven CM. A primary extraosseous Ewing sarcoma in the cerebellopontine angle of a child: review of relevant literature and case report. Neurosurgery 2010; 67: E1852–E1856. 5Tanboon J, Sitthinamsuwan B, Paruang T, Marrano P, Thorner PS. Primary intracranial Ewing sarcoma with an unusually aggressive course: a case report and review of the literature. Neuropathology 2012; 32: 293–300. 6Sandberg AA, Bridge JA. Updates on cytogenetics and molecular genetics of bone and soft tissue tumors: Ewing sarcoma and peripheral primitive neuroectodermal tumors. Cancer Genet Cytogenet 2000; 123: 1–26. 7Monument MJ, Bernthal NM, Randall RL. Salient features of mesenchymal stem cells-implications for Ewing sarcoma modeling. Front Oncol 2013; 3: 24. 8Lozito TP, Jackson WM, Nesti LJ, Tuan RS. Human mesenchymal stem cells generate a distinct pericellular zone of MMP activities via binding of MMPs and secretion of high levels of TIMPs. Matrix Biol 2014; 34: 132–143. 9Paul G, Özen I, Christophersen NS et al. The adult human brain harbors multipotent perivascular mesenchymal stem cells. PLoS One 2012; 7: e35577. 10de Alava E, Kawai A, Healey JH et al. EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma. J Clin Oncol 1998; 16: 1248–1255. Citing Literature Volume36, Issue5October 2016Pages 504-507 ReferencesRelatedInformation