{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,3]],"date-time":"2026-02-03T10:24:40Z","timestamp":1770114280715,"version":"3.49.0"},"reference-count":82,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"1","license":[{"start":{"date-parts":[[2025,1,6]],"date-time":"2025-01-06T00:00:00Z","timestamp":1736121600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Cosmet Laser Ther"],"published-print":{"date-parts":[[2025,1,6]]},"abstract":"<jats:sec>\n                    <jats:title>BACKGROUND<\/jats:title>\n                    <jats:p>The diagnosis of intracranial extraosseous Ewing\u2019s sarcoma (EES) poses challenges due to the absence of specific clinical and imaging features prior to surgery. It is crucial to differentiate the tumor from other small round cell malignancies postoperatively.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>OBSERVATIONS<\/jats:title>\n                    <jats:p>A 7-year-old patient was admitted to the authors\u2019 hospital due to the in situ recurrence of a posterior fossa tumor more than 1 month after the initial surgery for headache. Subsequently, a second surgery was performed at the authors\u2019 hospital, and pathological analysis indicated medulloblastoma. Genetic testing indicated Ewing\u2019s sarcoma. After 16 cycles of chemotherapy and 8 weeks of focal radiotherapy, the patient continued to exhibit clinical and radiographic remission. Whole-spine magnetic resonance imaging (MRI) revealed intraspinal enhancing lesions, which extended throughout the entire spinal canal. Palliative treatment was administered. The patient has been under observation for 2 months thus far, demonstrating disease stability as a result of the palliative treatment.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>LESSONS<\/jats:title>\n                    <jats:p>Primary intracranial EES is an exceptionally rare condition that can be easily misdiagnosed. Genetic testing is necessary to differentiate it from other small round cell tumors. Currently, a combination of surgery and chemoradiotherapy has proven to be an effective treatment approach. Postoperative follow-up should include MRI examination of the entire nervous system to detect any cerebrospinal fluid seeding metastasis and reduce mortality.<\/jats:p>\n                    <jats:p>\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/thejns.org\/doi\/10.3171\/CASE24488\">https:\/\/thejns.org\/doi\/10.3171\/CASE24488<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.3171\/case24488","type":"journal-article","created":{"date-parts":[[2025,1,6]],"date-time":"2025-01-06T01:47:03Z","timestamp":1736128023000},"source":"Crossref","is-referenced-by-count":1,"title":["Primary intracranial extraosseous Ewing\u2019s sarcoma with intraspinal metastasis in children: illustrative case"],"prefix":"10.3171","volume":"9","author":[{"given":"Wenjing","family":"Lu","sequence":"first","affiliation":[{"name":"Department of Neurosurgery, Children\u2019s Hospital of Nanjing Medical University, Nanjing, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tong","family":"Jin","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Children\u2019s Hospital of Nanjing Medical University, Nanjing, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xinfa","family":"Wang","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Children\u2019s Hospital of Nanjing Medical University, Nanjing, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rui","family":"Zhang","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Children\u2019s Hospital of Nanjing Medical University, Nanjing, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yongjie","family":"Zhu","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Children\u2019s Hospital of Nanjing Medical University, Nanjing, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1754","reference":[{"issue":"3","key":"bib1","series-title":"Nerv Syst Child","first-page":"303","article-title":"A case of peripheral PNET\/Ewing\u2019s sarcoma family tumor arising from cranial dura matter","volume":"47","author":"Hosoya","year":"2022","unstructured":"Hosoya TKambe AKamitani H, et al. 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