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...
Main Authors: | , , , , |
---|---|
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 |
id |
doaj-3909a4ae2df14d0b83520399d086e814 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT paulklimojr fibromyxomaofthelateralskullbaseinachildcasereport AT tusharjha fibromyxomaofthelateralskullbaseinachildcasereport AT asimfchoudhri fibromyxomaofthelateralskullbaseinachildcasereport AT roycejoyner fibromyxomaofthelateralskullbaseinachildcasereport AT lmadisonmichaelii fibromyxomaofthelateralskullbaseinachildcasereport |
_version_ |
1724605820438577152 |