Infrasellar craniopharyngioma: case report.Arq Neuropsiquiatr. 2001 Jun; 59(2-B):424-30.AN
Abstract
We report a case of infrasellar craniopharyngioma in a 34 year-old woman who presented with progressive headache and diplopia. Computed tomographic and magnetic resonance images showed a heterogeneous tumor originating from the sphenoid bone with ethmoid sinus and sella turcica extension. A sublabial rhinoseptal transsphenoidal surgery was performed. Craniopharyngiomas with infrasellar development are very rare. Infrasellar craniopharyngioma is uncommon, thirty-five cases has been reported in literature. The embryology, clinical features and radiographic investigation of these tumors are discussed.
Links
MeSH
Pub Type(s)
Case Reports
Journal Article
Review
Language
eng
PubMed ID
11460192
Citation
Falavigna, A, and J L. Kraemer. "Infrasellar Craniopharyngioma: Case Report." Arquivos De Neuro-psiquiatria, vol. 59, no. 2-B, 2001, pp. 424-30.
Falavigna A, Kraemer JL. Infrasellar craniopharyngioma: case report. Arq Neuropsiquiatr. 2001;59(2-B):424-30.
Falavigna, A., & Kraemer, J. L. (2001). Infrasellar craniopharyngioma: case report. Arquivos De Neuro-psiquiatria, 59(2-B), 424-30.
Falavigna A, Kraemer JL. Infrasellar Craniopharyngioma: Case Report. Arq Neuropsiquiatr. 2001;59(2-B):424-30. PubMed PMID: 11460192.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Infrasellar craniopharyngioma: case report.
AU - Falavigna,A,
AU - Kraemer,J L,
PY - 2001/7/19/pubmed
PY - 2001/8/17/medline
PY - 2001/7/19/entrez
SP - 424
EP - 30
JF - Arquivos de neuro-psiquiatria
JO - Arq Neuropsiquiatr
VL - 59
IS - 2-B
N2 - We report a case of infrasellar craniopharyngioma in a 34 year-old woman who presented with progressive headache and diplopia. Computed tomographic and magnetic resonance images showed a heterogeneous tumor originating from the sphenoid bone with ethmoid sinus and sella turcica extension. A sublabial rhinoseptal transsphenoidal surgery was performed. Craniopharyngiomas with infrasellar development are very rare. Infrasellar craniopharyngioma is uncommon, thirty-five cases has been reported in literature. The embryology, clinical features and radiographic investigation of these tumors are discussed.
SN - 0004-282X
UR - https://www.unboundmedicine.com/medline/citation/11460192/Infrasellar_craniopharyngioma:_case_report_
L2 - https://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2001000300022&lng=en&nrm=iso&tlng=en
DB - PRIME
DP - Unbound Medicine
ER -