{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,29]],"date-time":"2026-08-29T13:28:02Z","timestamp":1788010082473,"version":"build-2784847793"},"reference-count":9,"publisher":"Georg Thieme Verlag KG","issue":"03","license":[{"start":{"date-parts":[[2022,9,14]],"date-time":"2022-09-14T00:00:00Z","timestamp":1663113600000},"content-version":"vor","delay-in-days":1474,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Asian J Neurosurg"],"published-print":{"date-parts":[[2018,9]]},"abstract":"<jats:p>Atypical teratoid rhabdoid tumor (ATRT) is a rare, highly malignant tumor of the central nervous system, commonly affecting children below 3 years of age, with around 300 cases reported in the literature. Suprasellar area is a very rare location for such tumor in the pediatric population, with technical difficulties in complete excision. Third ventricular ATRT is very rare. Here, we report the case of a 2-year-old male child who presented with lethargy and vomiting. He had features of raised intracranial pressure with reduced vision in both eyes. Magnetic resonance imaging of the brain revealed a heterogeneously enhancing lobulated giant lesion in the suprasellar location, occupying the third ventricle and hypothalamus with encasement of both carotids. He underwent pericoronal parasagittal craniotomy, interhemispheric transcallosal interforniceal approach and gross total excision of the lesion. Postoperatively, the child had altered sensorium and diabetes insipidus, both of which recovered over a span of 10 days. Histopathological examination of the specimen was consistent with the diagnosis of World Health Organization Grade IV ATRT. In spite of all our efforts, he succumbed to his illness 5 months postoperatively.<\/jats:p>","DOI":"10.4103\/ajns.ajns_350_16","type":"journal-article","created":{"date-parts":[[2022,1,4]],"date-time":"2022-01-04T09:34:29Z","timestamp":1641288869000},"page":"873-876","source":"Crossref","is-referenced-by-count":4,"title":["Pediatric suprasellar atypical teratoid rhabdoid tumor arising from the third ventricle: A rare tumor at a very rare location"],"prefix":"10.1055","volume":"13","author":[{"given":"Joe","family":"Das","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mathew","family":"Abraham","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bevinahalli","family":"Nandeesh","sequence":"additional","affiliation":[{"name":"Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Suresh","family":"Nair","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"194","published-online":{"date-parts":[[2022,9,14]]},"reference":[{"key":"key-10.4103\/1793-5482.238065-1","first-page":"301","article-title":"Atypical teratoid rhabdoid tumors: A population-based clinical outcomes study involving 174 patients from the surveillance, epidemiology, and end results database (1973-2010)","author":"Lau","year":"2015","journal-title":"Cancer Manag Res"},{"key":"key-10.4103\/1793-5482.238065-2","doi-asserted-by":"crossref","first-page":"510","DOI":"10.2176\/nmc.39.510","article-title":"Clinicopathological characteristics of atypical teratoid\/rhabdoid tumor","author":"Oka","year":"1999","journal-title":"Neurol Med Chir (Tokyo)"},{"key":"key-10.4103\/1793-5482.238065-3","doi-asserted-by":"crossref","first-page":"382","DOI":"10.4103\/1817-1745.174455","article-title":"Atypical teratoid rhabdoid tumor of the lateral ventricle","author":"Darmoul","year":"2015","journal-title":"J Pediatr Neurosci","ISSN":"https:\/\/id.crossref.org\/issn\/1817-1745","issn-type":"print"},{"key":"key-10.4103\/1793-5482.238065-4","doi-asserted-by":"crossref","first-page":"108","DOI":"10.14791\/btrt.2014.2.2.108","article-title":"Adult-onset sellar and suprasellar atypical teratoid rhabdoid tumor treated with a multimodal approach: A case report","author":"Park","year":"2014","journal-title":"Brain Tumor Res Treat"},{"key":"key-10.4103\/1793-5482.238065-5","first-page":"448","article-title":"Atypical teratoid tumor of infancy: Definition of an entity","author":"Lefkowitz","year":"1987","journal-title":"Ann Neurol"},{"key":"key-10.4103\/1793-5482.238065-6","doi-asserted-by":"crossref","unstructured":"Lafay-Cousin L, Strother DR, Chan JA, Torchia J, Huang A. Atypical teratoid rhabdoid tumors. In: Scheinemann K, Bouffet E, editors. Pediatric Neuro-Oncology. 1st ed. New York: Springer; 2015. p. 163-71.","DOI":"10.1007\/978-1-4939-1541-5_15"},{"key":"key-10.4103\/1793-5482.238065-7","doi-asserted-by":"crossref","unstructured":"Biswas A, Goyal S, Puri T, Das P, Sarkar C, Julka PK, et al. Atypical teratoid rhabdoid tumor of the brain: Case series and review of literature. Childs Nerv Syst 2009;25:1495-500.","DOI":"10.1007\/s00381-009-0903-x"},{"key":"key-10.4103\/1793-5482.238065-8","first-page":"114","article-title":"Atypical teratoid rhabdoid tumor: Current therapy and future directions","author":"Ginn","year":"2012","journal-title":"Front Oncol"},{"key":"key-10.4103\/1793-5482.238065-9","doi-asserted-by":"crossref","unstructured":"Parwani AV, Stelow EB, Pambuccian SE, Burger PC, Ali SZ. Atypical teratoid\/rhabdoid tumor of the brain: Cytopathologic characteristics and differential diagnosis. Cancer 2005;105:65-70.","DOI":"10.1002\/cncr.20872"}],"container-title":["Asian Journal of Neurosurgery"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.thieme-connect.de\/products\/ejournals\/pdf\/10.4103\/ajns.AJNS_350_16.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,9,15]],"date-time":"2022-09-15T00:15:58Z","timestamp":1663200958000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.thieme-connect.de\/DOI\/DOI?10.4103\/ajns.AJNS_350_16"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,9]]},"references-count":9,"journal-issue":{"issue":"03","published-online":{"date-parts":[[2022,9,14]]},"published-print":{"date-parts":[[2018,9]]}},"URL":"https:\/\/doi.org\/10.4103\/ajns.ajns_350_16","archive":["Portico","CLOCKSS"],"relation":{},"ISSN":["1793-5482","2248-9614"],"issn-type":[{"value":"1793-5482","type":"print"},{"value":"2248-9614","type":"electronic"}],"subject":[],"published":{"date-parts":[[2018,9]]}}}