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Primary intracranial yolk sac tumor in the posterior fossa: Case report of a child with Down syndrome
Satge et al. summarized 38 central nervous system tumors in DS and reported that 14 (61%) of 23 cases under age 15 were germ cell tumors [3]. Robertson et al. reported the multimodal "sandwich" therapy, a course of PE (cisplatin and etoposide) therapy before radiation therapy and JEB proto...
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| Published in: | Clinical neurology and neurosurgery 2013-06, Vol.115 (6), p.811-813 |
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| cites | cdi_FETCH-LOGICAL-c543t-f9ad97774c2b6b9c0faedb860e97cc2b350332d41c795268cad563e6a283edb83 |
| container_end_page | 813 |
| container_issue | 6 |
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| container_title | Clinical neurology and neurosurgery |
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| creator | Endo, Shogo Kobayashi, Hiroyuki Terasaka, Shunsuke Iguchi, Akihiro Cho, Yuko Ohshima, Junjiro Kubota, Kanako Houkin, Kiyohiro |
| description | Satge et al. summarized 38 central nervous system tumors in DS and reported that 14 (61%) of 23 cases under age 15 were germ cell tumors [3]. Robertson et al. reported the multimodal "sandwich" therapy, a course of PE (cisplatin and etoposide) therapy before radiation therapy and JEB protocol (etoposide, carboplatin, bleomycin) after radiation therapy, to malignant GCTs resulted in 4-year actuarial event-free and total survival rates of 67 and 74%, respectively. |
| doi_str_mv | 10.1016/j.clineuro.2012.07.023 |
| format | article |
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Robertson et al. reported the multimodal "sandwich" therapy, a course of PE (cisplatin and etoposide) therapy before radiation therapy and JEB protocol (etoposide, carboplatin, bleomycin) after radiation therapy, to malignant GCTs resulted in 4-year actuarial event-free and total survival rates of 67 and 74%, respectively.</description><identifier>ISSN: 0303-8467</identifier><identifier>EISSN: 1872-6968</identifier><identifier>DOI: 10.1016/j.clineuro.2012.07.023</identifier><identifier>PMID: 22906817</identifier><identifier>CODEN: CNNSBV</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Brain cancer ; Chemoradiotherapy ; Child, Preschool ; Children & youth ; Chromosomes ; Combined Modality Therapy ; Cranial Fossa, Posterior - pathology ; Down syndrome ; Down Syndrome - complications ; Endodermal Sinus Tumor - pathology ; Endodermal Sinus Tumor - therapy ; Fetal Proteins - blood ; Germ cell tumor ; Humans ; Immunohistochemistry ; Magnetic Resonance Imaging ; Male ; Neurology ; Neurosurgery ; Neurosurgical Procedures ; Posterior fossa ; Radiation therapy ; Skull Base Neoplasms - pathology ; Skull Base Neoplasms - therapy ; Tumors ; Yolk sac tumor</subject><ispartof>Clinical neurology and neurosurgery, 2013-06, Vol.115 (6), p.811-813</ispartof><rights>Elsevier B.V.</rights><rights>2012 Elsevier B.V.</rights><rights>Copyright Elsevier Limited 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c543t-f9ad97774c2b6b9c0faedb860e97cc2b350332d41c795268cad563e6a283edb83</citedby><cites>FETCH-LOGICAL-c543t-f9ad97774c2b6b9c0faedb860e97cc2b350332d41c795268cad563e6a283edb83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22906817$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Endo, Shogo</creatorcontrib><creatorcontrib>Kobayashi, Hiroyuki</creatorcontrib><creatorcontrib>Terasaka, Shunsuke</creatorcontrib><creatorcontrib>Iguchi, Akihiro</creatorcontrib><creatorcontrib>Cho, Yuko</creatorcontrib><creatorcontrib>Ohshima, Junjiro</creatorcontrib><creatorcontrib>Kubota, Kanako</creatorcontrib><creatorcontrib>Houkin, Kiyohiro</creatorcontrib><title>Primary intracranial yolk sac tumor in the posterior fossa: Case report of a child with Down syndrome</title><title>Clinical neurology and neurosurgery</title><addtitle>Clin Neurol Neurosurg</addtitle><description>Satge et al. summarized 38 central nervous system tumors in DS and reported that 14 (61%) of 23 cases under age 15 were germ cell tumors [3]. 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| ispartof | Clinical neurology and neurosurgery, 2013-06, Vol.115 (6), p.811-813 |
| issn | 0303-8467 1872-6968 |
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| subjects | Brain cancer Chemoradiotherapy Child, Preschool Children & youth Chromosomes Combined Modality Therapy Cranial Fossa, Posterior - pathology Down syndrome Down Syndrome - complications Endodermal Sinus Tumor - pathology Endodermal Sinus Tumor - therapy Fetal Proteins - blood Germ cell tumor Humans Immunohistochemistry Magnetic Resonance Imaging Male Neurology Neurosurgery Neurosurgical Procedures Posterior fossa Radiation therapy Skull Base Neoplasms - pathology Skull Base Neoplasms - therapy Tumors Yolk sac tumor |
| title | Primary intracranial yolk sac tumor in the posterior fossa: Case report of a child with Down syndrome |
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