Clinicopathological study of seven cases of spinal cord teratoma: a possible germ cell origin
To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. Th...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
AL-Sarraj [verfasserIn] Parmar [verfasserIn] Dean [verfasserIn] |
|---|
| Format: |
E-Artikel |
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| Erschienen: |
Oxford, U.K. and Cambridge, USA: Blackwell Science Ltd ; 1998 |
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| Schlagwörter: |
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| Umfang: |
Online-Ressource |
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| Reproduktion: |
2001 ; Blackwell Publishing Journal Backfiles 1879-2005 |
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| Übergeordnetes Werk: |
In: Histopathology - Oxford [u.a.] : Wiley-Blackwell, 1977, 32(1998), 1, Seite 0 |
| Übergeordnetes Werk: |
volume:32 ; year:1998 ; number:1 ; pages:0 |
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| DOI / URN: |
10.1046/j.1365-2559.1998.00324.x |
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| 520 | |a To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. | ||
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10.1046/j.1365-2559.1998.00324.x doi (DE-627)NLEJ242775519 DE-627 ger DE-627 rakwb AL-Sarraj verfasserin aut Clinicopathological study of seven cases of spinal cord teratoma: a possible germ cell origin Oxford, U.K. and Cambridge, USA Blackwell Science Ltd 1998 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. 2001 Blackwell Publishing Journal Backfiles 1879-2005 |2001|||||||||| pathogenesis Parmar verfasserin aut Dean verfasserin aut Phookun oth Bridges oth In Histopathology Oxford [u.a.] : Wiley-Blackwell, 1977 32(1998), 1, Seite 0 Online-Ressource (DE-627)NLEJ243927045 (DE-600)2006447-0 1365-2559 nnns volume:32 year:1998 number:1 pages:0 http://dx.doi.org/10.1046/j.1365-2559.1998.00324.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 32 1998 1 0 |
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10.1046/j.1365-2559.1998.00324.x doi (DE-627)NLEJ242775519 DE-627 ger DE-627 rakwb AL-Sarraj verfasserin aut Clinicopathological study of seven cases of spinal cord teratoma: a possible germ cell origin Oxford, U.K. and Cambridge, USA Blackwell Science Ltd 1998 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. 2001 Blackwell Publishing Journal Backfiles 1879-2005 |2001|||||||||| pathogenesis Parmar verfasserin aut Dean verfasserin aut Phookun oth Bridges oth In Histopathology Oxford [u.a.] : Wiley-Blackwell, 1977 32(1998), 1, Seite 0 Online-Ressource (DE-627)NLEJ243927045 (DE-600)2006447-0 1365-2559 nnns volume:32 year:1998 number:1 pages:0 http://dx.doi.org/10.1046/j.1365-2559.1998.00324.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 32 1998 1 0 |
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10.1046/j.1365-2559.1998.00324.x doi (DE-627)NLEJ242775519 DE-627 ger DE-627 rakwb AL-Sarraj verfasserin aut Clinicopathological study of seven cases of spinal cord teratoma: a possible germ cell origin Oxford, U.K. and Cambridge, USA Blackwell Science Ltd 1998 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. 2001 Blackwell Publishing Journal Backfiles 1879-2005 |2001|||||||||| pathogenesis Parmar verfasserin aut Dean verfasserin aut Phookun oth Bridges oth In Histopathology Oxford [u.a.] : Wiley-Blackwell, 1977 32(1998), 1, Seite 0 Online-Ressource (DE-627)NLEJ243927045 (DE-600)2006447-0 1365-2559 nnns volume:32 year:1998 number:1 pages:0 http://dx.doi.org/10.1046/j.1365-2559.1998.00324.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 32 1998 1 0 |
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10.1046/j.1365-2559.1998.00324.x doi (DE-627)NLEJ242775519 DE-627 ger DE-627 rakwb AL-Sarraj verfasserin aut Clinicopathological study of seven cases of spinal cord teratoma: a possible germ cell origin Oxford, U.K. and Cambridge, USA Blackwell Science Ltd 1998 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. 2001 Blackwell Publishing Journal Backfiles 1879-2005 |2001|||||||||| pathogenesis Parmar verfasserin aut Dean verfasserin aut Phookun oth Bridges oth In Histopathology Oxford [u.a.] : Wiley-Blackwell, 1977 32(1998), 1, Seite 0 Online-Ressource (DE-627)NLEJ243927045 (DE-600)2006447-0 1365-2559 nnns volume:32 year:1998 number:1 pages:0 http://dx.doi.org/10.1046/j.1365-2559.1998.00324.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 32 1998 1 0 |
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10.1046/j.1365-2559.1998.00324.x doi (DE-627)NLEJ242775519 DE-627 ger DE-627 rakwb AL-Sarraj verfasserin aut Clinicopathological study of seven cases of spinal cord teratoma: a possible germ cell origin Oxford, U.K. and Cambridge, USA Blackwell Science Ltd 1998 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. 2001 Blackwell Publishing Journal Backfiles 1879-2005 |2001|||||||||| pathogenesis Parmar verfasserin aut Dean verfasserin aut Phookun oth Bridges oth In Histopathology Oxford [u.a.] : Wiley-Blackwell, 1977 32(1998), 1, Seite 0 Online-Ressource (DE-627)NLEJ243927045 (DE-600)2006447-0 1365-2559 nnns volume:32 year:1998 number:1 pages:0 http://dx.doi.org/10.1046/j.1365-2559.1998.00324.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 32 1998 1 0 |
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To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. |
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To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. |
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To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ242775519</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210707163909.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">120427s1998 xx |||||o 00| ||und c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1046/j.1365-2559.1998.00324.x</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ242775519</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">AL-Sarraj</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Clinicopathological study of seven cases of spinal cord teratoma: a possible germ cell origin</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Oxford, U.K. and Cambridge, USA</subfield><subfield code="b">Blackwell Science Ltd</subfield><subfield code="c">1998</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">To establish the clinical and pathological aspects of teratoma affecting the spinal cord.<section xml:id="abs1-2"><title type="main">Method and results:We reviewed our neurosurgical records for the last 15 years and found seven cases of teratoma of the spinal cord. The cases were reviewed clinically, radiologically and pathologically using immunohistochemical markers to identify various tissue components. We found that spinal cord teratoma is an extremely rare tumour of spinal cord affecting patients aged 23–47 years and of approximately equal male to female distribution. The terminal portions of spinal cord and intradural location of the tumour are common. Three cases were associated with vertebral anomaly. Most tumours showed benign (mature) components derived from more than one germ cell layer; one showed malignant adenocarcinomatous component. All cases were treated by surgical resection and two recurred at 6 and 10 year intervals without malignant transformation.<section xml:id="abs1-3"><title type="main">Conclusion:Spinal cord teratoma is a rare, mainly benign tumour, which could be associated with vertebral anomaly. The pathogenesis of this tumour is controversial, possibly due to germinal cell aberration.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="d">2001</subfield><subfield code="f">Blackwell Publishing Journal Backfiles 1879-2005</subfield><subfield code="7">|2001||||||||||</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">pathogenesis</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Parmar</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dean</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Phookun</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bridges</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Histopathology</subfield><subfield code="d">Oxford [u.a.] : Wiley-Blackwell, 1977</subfield><subfield code="g">32(1998), 1, Seite 0</subfield><subfield code="h">Online-Ressource</subfield><subfield code="w">(DE-627)NLEJ243927045</subfield><subfield code="w">(DE-600)2006447-0</subfield><subfield code="x">1365-2559</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:32</subfield><subfield code="g">year:1998</subfield><subfield code="g">number:1</subfield><subfield code="g">pages:0</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1046/j.1365-2559.1998.00324.x</subfield><subfield code="q">text/html</subfield><subfield code="x">Verlag</subfield><subfield code="z">Deutschlandweit zugänglich</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-DJB</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">32</subfield><subfield code="j">1998</subfield><subfield code="e">1</subfield><subfield code="h">0</subfield></datafield></record></collection>
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