{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,12]],"date-time":"2026-05-12T06:59:07Z","timestamp":1778569147902,"version":"3.51.4"},"reference-count":12,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["PED"],"published-print":{"date-parts":[[2010,6]]},"abstract":"<jats:p>Pineal tumors are rare neoplasms that are categorized into pineoblastomas, pineocytomas, and pineal parenchymal tumors of intermediate differentiation. Pineal anlage tumors are primary pineal tumors with neuroepithelial and ectomesenchymal differentiation and without endodermal differentiation. The authors review the literature and report the case of a 5-month-old boy with a pineal anlage tumor. This is only the sixth case of a pineal anlage tumor reported in the English-language literature adding to the understanding of this tumor's presentation, immunomorphological and molecular characteristics, embryological origin, radiological appearance, treatment outcome, and prognosis.<\/jats:p>","DOI":"10.3171\/2010.2.peds09294","type":"journal-article","created":{"date-parts":[[2010,6,1]],"date-time":"2010-06-01T13:59:20Z","timestamp":1275400760000},"page":"636-640","source":"Crossref","is-referenced-by-count":9,"title":["Pineal anlage tumor in a 5-month-old boy"],"prefix":"10.3171","volume":"5","author":[{"given":"Joffre E.","family":"Olaya","sequence":"first","affiliation":[{"name":"Departments of Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ravi","family":"Raghavan","sequence":"additional","affiliation":[{"name":"Pathology, Loma Linda University Medical Center, Loma Linda, California"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Laura","family":"Totaro","sequence":"additional","affiliation":[{"name":"Departments of Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexander","family":"Zouros","sequence":"additional","affiliation":[{"name":"Departments of Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1754","reference":[{"key":"b1-0050636","series-title":"Arch Pathol Lab Med","doi-asserted-by":"publisher","first-page":"1233","DOI":"10.5858\/2006-130-1233-ROPATW","article-title":"Review of pineal anlage tumor with divergent histology","volume":"130","author":"Berns","year":"2006"},{"key":"b2-0050636","series-title":"J Anat","first-page":"28","article-title":"The human pineal gland and pineal cysts","volume":"67","author":"Cooper","year":"1932"},{"key":"b3-0050636","series-title":"Brain Pathol","doi-asserted-by":"publisher","first-page":"304","DOI":"10.1111\/j.1750-3639.2007.00084.x","article-title":"The 2007 Revised World Health Organization (WHO) Classification of Tumours of the Central Nervous System: newly codified entities","volume":"17","author":"Fuller","year":"2007"},{"key":"b4-0050636","series-title":"J Neurooncol","doi-asserted-by":"publisher","first-page":"89","DOI":"10.1007\/s11060-008-9589-2","article-title":"Outcome of pediatric pineoblastoma after surgery, radiation and chemotherapy","volume":"89","author":"Gilheeney","year":"2008"},{"key":"b5-0050636","series-title":"Brain Pathol","first-page":"263","article-title":"A 10-month-old boy with a large pineal tumor","volume":"15","author":"Gudinaviciene","year":"2005"},{"key":"b6-0050636","series-title":"Cancer","doi-asserted-by":"publisher","first-page":"2486","DOI":"10.1002\/1097-0142(197706)39:6<2486::AID-CNCR2820390627>3.0.CO;2-E","article-title":"Ectomesenchymoma. 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