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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.

Authors+Show Affiliations

Disciplina de Neurologia, Faculdade de Medicina, Universidade de Caxias do Sul, Sao Paulo, Brazil. asdrubal@doctor.comNo affiliation info available

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 -