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

Abstract 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 histor...

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Main Authors: Paul Klimo Jr., Tushar Jha, Asim F. Choudhri, Royce Joyner, L. Madison Michael II
Format: Article
Language:English
Published: Georg Thieme Verlag KG 2013-07-01
Series:Journal of Neurological Surgery Reports
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0033-1351115
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spelling doaj-3909a4ae2df14d0b83520399d086e8142020-11-25T03:23:32ZengGeorg Thieme Verlag KGJournal of Neurological Surgery Reports2193-63582193-63662013-07-01740210511010.1055/s-0033-1351115Fibromyxoma of the Lateral Skull Base in a Child: Case ReportPaul Klimo Jr.0Tushar Jha1Asim F. Choudhri2Royce Joyner3L. Madison Michael II4Murphey Neurologic & Spine Institute, Semmes, Memphis, Tennessee, United StatesDepartment of Neurosurgery, Georgetown University, Washington, District of Columbia, United StatesLe Bonheur Children's Hospital, Memphis, Tennessee, United StatesLe Bonheur Children's Hospital, Memphis, Tennessee, United StatesMurphey Neurologic & Spine Institute, Semmes, Memphis, Tennessee, United StatesAbstract 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.http://www.thieme-connect.de/DOI/DOI?10.1055/s-0033-1351115fibromyxomamyxomachildpediatricskull basepetrousmesenchymaltumorbenign
collection DOAJ
language English
format Article
sources DOAJ
author Paul Klimo Jr.
Tushar Jha
Asim F. Choudhri
Royce Joyner
L. Madison Michael II
spellingShingle Paul Klimo Jr.
Tushar Jha
Asim F. Choudhri
Royce Joyner
L. Madison Michael II
Fibromyxoma of the Lateral Skull Base in a Child: Case Report
Journal of Neurological Surgery Reports
fibromyxoma
myxoma
child
pediatric
skull base
petrous
mesenchymal
tumor
benign
author_facet Paul Klimo Jr.
Tushar Jha
Asim F. Choudhri
Royce Joyner
L. Madison Michael II
author_sort Paul Klimo Jr.
title 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_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_sort fibromyxoma of the lateral skull base in a child: case report
publisher Georg Thieme Verlag KG
series Journal of Neurological Surgery Reports
issn 2193-6358
2193-6366
publishDate 2013-07-01
description Abstract 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.
topic fibromyxoma
myxoma
child
pediatric
skull base
petrous
mesenchymal
tumor
benign
url http://www.thieme-connect.de/DOI/DOI?10.1055/s-0033-1351115
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