{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,6,11]],"date-time":"2025-06-11T09:30:36Z","timestamp":1749634236957},"reference-count":21,"publisher":"Cambridge University Press (CUP)","issue":"3","license":[{"start":{"date-parts":[[2015,9,18]],"date-time":"2015-09-18T00:00:00Z","timestamp":1442534400000},"content-version":"unspecified","delay-in-days":7718,"URL":"https:\/\/www.cambridge.org\/core\/terms"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Can. j. neurol. sci."],"published-print":{"date-parts":[[1994,8]]},"abstract":"<jats:title>Abstract:<\/jats:title><jats:p>A 9-month-old male presented to hospital with signs and symptoms of raised intracranial pressure. A CT scan showed obstructive hydrocephalus from a large pineal region mass lesion into which an intratumoral hemorrhage had occurred. A posterior fossa craniectomy and subtotal excision of the mass lesion were performed. By histopathology, the lesion was a malignant rhabdoid tumour (MRT). Despite surgery and chemotherapy, the tumour grew inexorably, and the patient died four months after the initial diagnosis. MRT is a rare and highly invasive neoplasm which infrequently arises from the central nervous system. This is the first documented case of a MRT arising from the pineal region. The clinical, radiographic, and pathological features of the MRT in this patient are presented.<\/jats:p>","DOI":"10.1017\/s0317167100041287","type":"journal-article","created":{"date-parts":[[2016,2,17]],"date-time":"2016-02-17T09:19:53Z","timestamp":1455700793000},"page":"273-277","source":"Crossref","is-referenced-by-count":20,"title":["Malignant Rhabdoid Tumour of the Pineal Region"],"prefix":"10.1017","volume":"21","author":[{"given":"Matthew","family":"Muller","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sherri Lynn","family":"Hubbard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John","family":"Provias","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mark","family":"Greenberg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Laurence E.","family":"Becker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James T.","family":"Rutka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"56","published-online":{"date-parts":[[2015,9,18]]},"reference":[{"key":"S0317167100041287_ref470","first-page":"84","article-title":"Malignant thymic tumour in an infant (malignant histiocytoma)","volume":"102","author":"Lemos","year":"1978","journal-title":"Arch Pathol Lab Med"},{"key":"S0317167100041287_ref469","doi-asserted-by":"crossref","first-page":"589","DOI":"10.1242\/jcs.103.2.589","article-title":"Characterization of the human nestin gene reveals a close evolutionary relationship to neurofilaments","volume":"103","author":"Dahlstrand","year":"1992","journal-title":"J Cell Science"},{"key":"S0317167100041287_ref467","doi-asserted-by":"publisher","DOI":"10.1002\/gcc.2870050203"},{"key":"S0317167100041287_ref461","first-page":"1","article-title":"Primary CNS malignant rhabdoid tumour (MRT); 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