Successful treatment of neoadjuvant therapy for papillary tumor of the pineal region
We report a boy who in 1994, at the age of 11, presented with headache and vomiting. The fi nal diagnosis was papillary tumor of the pineal region (PTPR). Magnetic resonance imaging (MRI) revealed a heterogeneous mass. Hydrocephalus was addressed by immediate ventricle drainage; subsequently, we att...
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| Veröffentlicht in: | Brain tumor pathology 2009-10, Vol.26 (2), p.73-77 |
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| creator | Nakamura, Hideo Makino, Keishi Kochi, Masato Nakazato, Yoichi Kuratsu, Jun-ichi |
| description | We report a boy who in 1994, at the age of 11, presented with headache and vomiting. The fi nal diagnosis was papillary tumor of the pineal region (PTPR). Magnetic resonance imaging (MRI) revealed a heterogeneous mass. Hydrocephalus was addressed by immediate ventricle drainage; subsequently, we attempted tumor removal. As the intraoperative diagnosis of the hemorrhagic tumor was primitive neuroectodermal tumor (PNET), we did not proceed to total removal. After the delivery of radiotherapy (50.4 Gy) and one course of Nimustine hydrochloride (ACNU) chemotherapy, the residual tumor was completely resected. The diagnosis at that time (1994) was papillary pineocytoma. He was followed on an outpatient basis for 15 years and remained free of recurrence. This type of tumor was later proposed to represent a new distinct tumor subtype, papillary tumor of the pineal region (PTPR). Our data indicate that our patient’s tumor should be included in this category. |
| doi_str_mv | 10.1007/s10014-009-0250-3 |
| format | Article |
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The fi nal diagnosis was papillary tumor of the pineal region (PTPR). Magnetic resonance imaging (MRI) revealed a heterogeneous mass. Hydrocephalus was addressed by immediate ventricle drainage; subsequently, we attempted tumor removal. As the intraoperative diagnosis of the hemorrhagic tumor was primitive neuroectodermal tumor (PNET), we did not proceed to total removal. After the delivery of radiotherapy (50.4 Gy) and one course of Nimustine hydrochloride (ACNU) chemotherapy, the residual tumor was completely resected. The diagnosis at that time (1994) was papillary pineocytoma. He was followed on an outpatient basis for 15 years and remained free of recurrence. This type of tumor was later proposed to represent a new distinct tumor subtype, papillary tumor of the pineal region (PTPR). Our data indicate that our patient’s tumor should be included in this category.</description><identifier>ISSN: 1433-7398</identifier><identifier>EISSN: 1861-387X</identifier><identifier>DOI: 10.1007/s10014-009-0250-3</identifier><identifier>PMID: 19856218</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Brain Neoplasms - diagnosis ; Brain Neoplasms - pathology ; Brain Neoplasms - therapy ; Cancer Research ; Carcinoma, Papillary - diagnosis ; Carcinoma, Papillary - pathology ; Carcinoma, Papillary - therapy ; Child ; Humans ; Hydrocephalus - therapy ; Image Processing, Computer-Assisted ; Magnetic Resonance Imaging ; Male ; Medicine ; Medicine & Public Health ; Neoadjuvant Therapy ; Neurology ; Neurosurgery ; Neurosurgical Procedures ; Nimustine - therapeutic use ; Oncology ; Original Article ; Pathology ; Pineal Gland - pathology ; Pineal Gland - surgery ; Pinealoma - diagnosis ; Pinealoma - pathology ; Pinealoma - therapy ; Treatment Outcome</subject><ispartof>Brain tumor pathology, 2009-10, Vol.26 (2), p.73-77</ispartof><rights>Japan Soceity of BrainTumor Pathology 2009</rights><rights>Japan Soceity of BrainTumor Pathology 2009.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-908998762630f94e51de6169c0d6c4b2d3243121e8078173944b42199daca1db3</citedby><cites>FETCH-LOGICAL-c426t-908998762630f94e51de6169c0d6c4b2d3243121e8078173944b42199daca1db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10014-009-0250-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2917924475?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,781,785,21390,21391,27926,27927,33532,33533,33746,33747,41490,42559,43661,43807,51321,64387,64389,64391,72471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19856218$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakamura, Hideo</creatorcontrib><creatorcontrib>Makino, Keishi</creatorcontrib><creatorcontrib>Kochi, Masato</creatorcontrib><creatorcontrib>Nakazato, Yoichi</creatorcontrib><creatorcontrib>Kuratsu, Jun-ichi</creatorcontrib><title>Successful treatment of neoadjuvant therapy for papillary tumor of the pineal region</title><title>Brain tumor pathology</title><addtitle>Brain Tumor Pathol</addtitle><addtitle>Brain Tumor Pathol</addtitle><description>We report a boy who in 1994, at the age of 11, presented with headache and vomiting. The fi nal diagnosis was papillary tumor of the pineal region (PTPR). Magnetic resonance imaging (MRI) revealed a heterogeneous mass. Hydrocephalus was addressed by immediate ventricle drainage; subsequently, we attempted tumor removal. As the intraoperative diagnosis of the hemorrhagic tumor was primitive neuroectodermal tumor (PNET), we did not proceed to total removal. After the delivery of radiotherapy (50.4 Gy) and one course of Nimustine hydrochloride (ACNU) chemotherapy, the residual tumor was completely resected. The diagnosis at that time (1994) was papillary pineocytoma. He was followed on an outpatient basis for 15 years and remained free of recurrence. This type of tumor was later proposed to represent a new distinct tumor subtype, papillary tumor of the pineal region (PTPR). Our data indicate that our patient’s tumor should be included in this category.</description><subject>Brain Neoplasms - diagnosis</subject><subject>Brain Neoplasms - pathology</subject><subject>Brain Neoplasms - therapy</subject><subject>Cancer Research</subject><subject>Carcinoma, Papillary - diagnosis</subject><subject>Carcinoma, Papillary - pathology</subject><subject>Carcinoma, Papillary - therapy</subject><subject>Child</subject><subject>Humans</subject><subject>Hydrocephalus - therapy</subject><subject>Image Processing, Computer-Assisted</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neoadjuvant Therapy</subject><subject>Neurology</subject><subject>Neurosurgery</subject><subject>Neurosurgical Procedures</subject><subject>Nimustine - therapeutic use</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Pathology</subject><subject>Pineal Gland - pathology</subject><subject>Pineal Gland - surgery</subject><subject>Pinealoma - diagnosis</subject><subject>Pinealoma - pathology</subject><subject>Pinealoma - therapy</subject><subject>Treatment Outcome</subject><issn>1433-7398</issn><issn>1861-387X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kVtLJDEQhYO4eBn9Ab5Ig6BPvVuVpHN5lMFdBcGHdcG3kOlOaw99M-kW_PdbwwwIgr4kKerLyakcxs4QfiKA_pVoRZkD2Bx4AbnYY0doFObC6Kd9Okshci2sOWTHKa0BpASNB-wQrSkUR3PEHv_OZRlSquc2m2LwUxf6KRvqrA-Dr9bzm6dyegnRj-9ZPcRs9GPTtj6-Z9PcUU0otbOx6YNvsxiem6E_YT9q36ZwutsX7N_vm8flbX7_8OdueX2fl5KrKbdgrDVacSWgtjIUWAWFypZQqVKueCW4FMgxGNAGaQ4pV5KjtZUvPVYrsWBXW90xDq9zSJPrmlQGskfu5-QscFGYggsiL78llVZWg9UEXnwC18Mce5rCcYvacil1QRRuqTIOKcVQuzE2HX2KQ3CbaNw2GkfRuE00bmPhfKc8r7pQfdzYZUEA3wKJWv1ziB9Pf636H6ool7E</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Nakamura, Hideo</creator><creator>Makino, Keishi</creator><creator>Kochi, Masato</creator><creator>Nakazato, Yoichi</creator><creator>Kuratsu, Jun-ichi</creator><general>Springer Japan</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20091001</creationdate><title>Successful treatment of neoadjuvant therapy for papillary tumor of the pineal region</title><author>Nakamura, Hideo ; Makino, Keishi ; Kochi, Masato ; Nakazato, Yoichi ; Kuratsu, Jun-ichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-908998762630f94e51de6169c0d6c4b2d3243121e8078173944b42199daca1db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Brain Neoplasms - diagnosis</topic><topic>Brain Neoplasms - pathology</topic><topic>Brain Neoplasms - therapy</topic><topic>Cancer Research</topic><topic>Carcinoma, Papillary - diagnosis</topic><topic>Carcinoma, Papillary - pathology</topic><topic>Carcinoma, Papillary - therapy</topic><topic>Child</topic><topic>Humans</topic><topic>Hydrocephalus - therapy</topic><topic>Image Processing, Computer-Assisted</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neoadjuvant Therapy</topic><topic>Neurology</topic><topic>Neurosurgery</topic><topic>Neurosurgical Procedures</topic><topic>Nimustine - therapeutic use</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Pathology</topic><topic>Pineal Gland - pathology</topic><topic>Pineal Gland - surgery</topic><topic>Pinealoma - diagnosis</topic><topic>Pinealoma - pathology</topic><topic>Pinealoma - therapy</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakamura, Hideo</creatorcontrib><creatorcontrib>Makino, Keishi</creatorcontrib><creatorcontrib>Kochi, Masato</creatorcontrib><creatorcontrib>Nakazato, Yoichi</creatorcontrib><creatorcontrib>Kuratsu, Jun-ichi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Brain tumor pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakamura, Hideo</au><au>Makino, Keishi</au><au>Kochi, Masato</au><au>Nakazato, Yoichi</au><au>Kuratsu, Jun-ichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Successful treatment of neoadjuvant therapy for papillary tumor of the pineal region</atitle><jtitle>Brain tumor pathology</jtitle><stitle>Brain Tumor Pathol</stitle><addtitle>Brain Tumor Pathol</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>26</volume><issue>2</issue><spage>73</spage><epage>77</epage><pages>73-77</pages><issn>1433-7398</issn><eissn>1861-387X</eissn><abstract>We report a boy who in 1994, at the age of 11, presented with headache and vomiting. The fi nal diagnosis was papillary tumor of the pineal region (PTPR). Magnetic resonance imaging (MRI) revealed a heterogeneous mass. Hydrocephalus was addressed by immediate ventricle drainage; subsequently, we attempted tumor removal. As the intraoperative diagnosis of the hemorrhagic tumor was primitive neuroectodermal tumor (PNET), we did not proceed to total removal. After the delivery of radiotherapy (50.4 Gy) and one course of Nimustine hydrochloride (ACNU) chemotherapy, the residual tumor was completely resected. The diagnosis at that time (1994) was papillary pineocytoma. He was followed on an outpatient basis for 15 years and remained free of recurrence. This type of tumor was later proposed to represent a new distinct tumor subtype, papillary tumor of the pineal region (PTPR). 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| subjects | Brain Neoplasms - diagnosis Brain Neoplasms - pathology Brain Neoplasms - therapy Cancer Research Carcinoma, Papillary - diagnosis Carcinoma, Papillary - pathology Carcinoma, Papillary - therapy Child Humans Hydrocephalus - therapy Image Processing, Computer-Assisted Magnetic Resonance Imaging Male Medicine Medicine & Public Health Neoadjuvant Therapy Neurology Neurosurgery Neurosurgical Procedures Nimustine - therapeutic use Oncology Original Article Pathology Pineal Gland - pathology Pineal Gland - surgery Pinealoma - diagnosis Pinealoma - pathology Pinealoma - therapy Treatment Outcome |
| title | Successful treatment of neoadjuvant therapy for papillary tumor of the pineal region |
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