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Fibromyxoma of the Lateral Skull Base in a Child: Case Report

Purpose Fibromyxomas and myxomas are benign tumors of mesenchymal origin usually found outside the nervous system, most commonly in the atrium of the heart. They can also arise in the mandible or maxilla, but it is exceedingly rare to find them within the skull base. The history, histologic features...

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Autores principales: Klimo, Paul, Jha, Tushar, Choudhri, Asim F., Joyner, Royce, Michael, L. Madison
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836972/
https://www.ncbi.nlm.nih.gov/pubmed/24303345
http://dx.doi.org/10.1055/s-0033-1351115
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author Klimo, Paul
Jha, Tushar
Choudhri, Asim F.
Joyner, Royce
Michael, L. Madison
author_facet Klimo, Paul
Jha, Tushar
Choudhri, Asim F.
Joyner, Royce
Michael, L. Madison
author_sort Klimo, Paul
collection PubMed
description Purpose Fibromyxomas and myxomas are benign tumors of mesenchymal origin usually found outside the nervous system, most commonly in the atrium of the heart. They can also arise in the mandible or maxilla, but it is exceedingly rare to find them within the skull base. The history, histologic features, and the literature, with emphasis on other pediatric cases, are reviewed for this uncommon skull base neoplasm. Methods We describe the case of a 13-year-old girl who presented with a 1-year history of facial weakness, numbness, and hearing loss. A large locally destructive tumor centered in the petrous bone was found on magnetic resonance imaging. Results A mastoidectomy combined with a middle fossa craniotomy was performed for gross total resection. The child is disease free 12 months after surgery. Conclusion Diagnosis could not be made solely on radiographic studies because of the lack of pathognomonic imaging features. Radical resection provided the patient the best chance of cure. Long-term surveillance is necessary to monitor for tumor recurrence.
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spelling pubmed-38369722013-12-03 Fibromyxoma of the Lateral Skull Base in a Child: Case Report Klimo, Paul Jha, Tushar Choudhri, Asim F. Joyner, Royce Michael, L. Madison J Neurol Surg Rep Article Purpose Fibromyxomas and myxomas are benign tumors of mesenchymal origin usually found outside the nervous system, most commonly in the atrium of the heart. They can also arise in the mandible or maxilla, but it is exceedingly rare to find them within the skull base. The history, histologic features, and the literature, with emphasis on other pediatric cases, are reviewed for this uncommon skull base neoplasm. Methods We describe the case of a 13-year-old girl who presented with a 1-year history of facial weakness, numbness, and hearing loss. A large locally destructive tumor centered in the petrous bone was found on magnetic resonance imaging. Results A mastoidectomy combined with a middle fossa craniotomy was performed for gross total resection. The child is disease free 12 months after surgery. Conclusion Diagnosis could not be made solely on radiographic studies because of the lack of pathognomonic imaging features. Radical resection provided the patient the best chance of cure. Long-term surveillance is necessary to monitor for tumor recurrence. Georg Thieme Verlag KG 2013-07-30 2013-12 /pmc/articles/PMC3836972/ /pubmed/24303345 http://dx.doi.org/10.1055/s-0033-1351115 Text en © Thieme Medical Publishers
spellingShingle Article
Klimo, Paul
Jha, Tushar
Choudhri, Asim F.
Joyner, Royce
Michael, L. Madison
Fibromyxoma of the Lateral Skull Base in a Child: Case Report
title Fibromyxoma of the Lateral Skull Base in a Child: Case Report
title_full Fibromyxoma of the Lateral Skull Base in a Child: Case Report
title_fullStr Fibromyxoma of the Lateral Skull Base in a Child: Case Report
title_full_unstemmed Fibromyxoma of the Lateral Skull Base in a Child: Case Report
title_short Fibromyxoma of the Lateral Skull Base in a Child: Case Report
title_sort fibromyxoma of the lateral skull base in a child: case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836972/
https://www.ncbi.nlm.nih.gov/pubmed/24303345
http://dx.doi.org/10.1055/s-0033-1351115
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