Paragangliomas of the parasellar region.
Identifieur interne : 000774 ( PubMed/Corpus ); précédent : 000773; suivant : 000775Paragangliomas of the parasellar region.
Auteurs : F. Hertel ; M. Bettag ; M. Mörsdorf ; W. FeidenSource :
- Neurosurgical review [ 0344-5607 ] ; 2003.
English descriptors
- KwdEn :
- Female, Humans, Middle Aged, Paraganglioma (diagnostic imaging), Paraganglioma (pathology), Paraganglioma (surgery), Radiography, Sella Turcica (diagnostic imaging), Sella Turcica (pathology), Sella Turcica (surgery), Skull Neoplasms (diagnostic imaging), Skull Neoplasms (pathology), Skull Neoplasms (surgery).
- MESH :
- diagnostic imaging : Paraganglioma, Sella Turcica, Skull Neoplasms.
- pathology : Paraganglioma, Sella Turcica, Skull Neoplasms.
- surgery : Paraganglioma, Sella Turcica, Skull Neoplasms.
- Female, Humans, Middle Aged, Radiography.
Abstract
Parasellar paragangliomas are rare tumors. As far as we know, only ten cases are described in the literature. Their clinical, pathological, and radiological features and possible origin are discussed in this article and a review of the literature is given. Additionally, we report a new case of a 51-year-old woman with paraganglioma growing in the anterior, middle, and posterior cranial fossa with extended destruction of the skull base. The patient had been suffering from long-standing headaches and facial nerve paresis. Preoperatively, this tumor was suspected to be a meningioma.
DOI: 10.1007/s10143-003-0266-9
PubMed: 12690532
Links to Exploration step
pubmed:12690532Le document en format XML
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<author><name sortKey="Hertel, F" sort="Hertel, F" uniqKey="Hertel F" first="F" last="Hertel">F. Hertel</name>
<affiliation><nlm:affiliation>Department of Neurosurgery, Krankenhaus der Barmherzigen Brüder, Nordallee 1, 54292 Trier, Germany. f.hertel@bk-trier.de</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Bettag, M" sort="Bettag, M" uniqKey="Bettag M" first="M" last="Bettag">M. Bettag</name>
</author>
<author><name sortKey="Morsdorf, M" sort="Morsdorf, M" uniqKey="Morsdorf M" first="M" last="Mörsdorf">M. Mörsdorf</name>
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<author><name sortKey="Feiden, W" sort="Feiden, W" uniqKey="Feiden W" first="W" last="Feiden">W. Feiden</name>
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<author><name sortKey="Hertel, F" sort="Hertel, F" uniqKey="Hertel F" first="F" last="Hertel">F. Hertel</name>
<affiliation><nlm:affiliation>Department of Neurosurgery, Krankenhaus der Barmherzigen Brüder, Nordallee 1, 54292 Trier, Germany. f.hertel@bk-trier.de</nlm:affiliation>
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<author><name sortKey="Bettag, M" sort="Bettag, M" uniqKey="Bettag M" first="M" last="Bettag">M. Bettag</name>
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<author><name sortKey="Morsdorf, M" sort="Morsdorf, M" uniqKey="Morsdorf M" first="M" last="Mörsdorf">M. Mörsdorf</name>
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<author><name sortKey="Feiden, W" sort="Feiden, W" uniqKey="Feiden W" first="W" last="Feiden">W. Feiden</name>
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<series><title level="j">Neurosurgical review</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Paraganglioma (diagnostic imaging)</term>
<term>Paraganglioma (pathology)</term>
<term>Paraganglioma (surgery)</term>
<term>Radiography</term>
<term>Sella Turcica (diagnostic imaging)</term>
<term>Sella Turcica (pathology)</term>
<term>Sella Turcica (surgery)</term>
<term>Skull Neoplasms (diagnostic imaging)</term>
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<term>Skull Neoplasms</term>
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<keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Paraganglioma</term>
<term>Sella Turcica</term>
<term>Skull Neoplasms</term>
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<front><div type="abstract" xml:lang="en">Parasellar paragangliomas are rare tumors. As far as we know, only ten cases are described in the literature. Their clinical, pathological, and radiological features and possible origin are discussed in this article and a review of the literature is given. Additionally, we report a new case of a 51-year-old woman with paraganglioma growing in the anterior, middle, and posterior cranial fossa with extended destruction of the skull base. The patient had been suffering from long-standing headaches and facial nerve paresis. Preoperatively, this tumor was suspected to be a meningioma.</div>
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<Abstract><AbstractText>Parasellar paragangliomas are rare tumors. As far as we know, only ten cases are described in the literature. Their clinical, pathological, and radiological features and possible origin are discussed in this article and a review of the literature is given. Additionally, we report a new case of a 51-year-old woman with paraganglioma growing in the anterior, middle, and posterior cranial fossa with extended destruction of the skull base. The patient had been suffering from long-standing headaches and facial nerve paresis. Preoperatively, this tumor was suspected to be a meningioma.</AbstractText>
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