{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,12]],"date-time":"2026-05-12T07:00:59Z","timestamp":1778569259906,"version":"3.51.4"},"reference-count":26,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2024,8,8]],"date-time":"2024-08-08T00:00:00Z","timestamp":1723075200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Oncol."],"abstract":"<jats:p>Solitary fibrous tumor (SFT) is a type of fibroblastic neoplasm that can occur in various parts of the body, with SFT of the pineal gland being exceedingly rare. We report the case of a 58-year-old male presenting with recurrent hiccups, acid reflux, and headache. Magnetic resonance imaging revealed an occupying lesion in the pineal region, suggestive of a neoplastic process. Intraoperatively, the lesion was located in the pineal region, exhibiting a grayish-red color, and was largely resected. Pathological examination confirmed the diagnosis of solitary fibrous tumor (CNS WHO Grade 1). Postoperatively, the patient was supplemented with radiotherapy, and long-term follow-up showed no signs of recurrence or metastasis.<\/jats:p>","DOI":"10.3389\/fonc.2024.1392540","type":"journal-article","created":{"date-parts":[[2024,8,8]],"date-time":"2024-08-08T04:56:22Z","timestamp":1723092982000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":2,"title":["Solitary fibrous tumor of the pineal gland: a case report and review of the literature"],"prefix":"10.3389","volume":"14","author":[{"given":"Yixiao","family":"He","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pengchen","family":"He","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anqun","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuzhu","family":"Ji","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gang","family":"Xie","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lili","family":"Zou","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1965","published-online":{"date-parts":[[2024,8,8]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","DOI":"10.1093\/neuonc\/noab106","article-title":"The 2021 who classification of tumors of the central nervous system: A summary","volume":"23","author":"Louis","year":"2021","journal-title":"Neuro-oncology"},{"key":"B2","doi-asserted-by":"publisher","DOI":"10.1097\/pai.0000000000000745","article-title":"Stat6 expression in solitary fibrous tumor and histologic mimics: A single institution experience","volume":"28","author":"Saeed","year":"2020","journal-title":"Appl immunohistochem Mol morphology: AIMM"},{"key":"B3","doi-asserted-by":"publisher","DOI":"10.3760\/cma.j.issn.0529\u20135807.2017.07.004","article-title":"Solitary fibrous tumor\/hemangiopericytoma of central nervous system: A clinicopathologic analysis of 71 cases","volume":"46","author":"Li","year":"2017","journal-title":"Zhonghua bing li xue za zhi = Chin J Pathol"},{"key":"B4","doi-asserted-by":"publisher","DOI":"10.1007\/s00401\u2013016-1545\u20131","article-title":"The 2016 world health organization classification of tumors of the central nervous system: A summary","volume":"131","author":"Louis","year":"2016","journal-title":"Acta neuropathol"},{"key":"B5","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1002\/ajim.4700220103","article-title":"Primary neoplasms of the pleura. 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