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Traumatic rupture of an intracranial dermoid cyst: Case report and literature review

BACKGROUND: Dermoid tumors are benign congenital cystic lesions that usually present with local mass effect. Very rarely, they present as spontaneous ruptures. Traumatic rupture of these dermoid cysts is an extremely rare event and only a handful of such cases have been ever reported. CASE DESCRIPTI...

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Autores principales: Esquenazi, Yoshua, Kerr, Keith, Bhattacharjee, Meenakshi B., Tandon, Nitin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707326/
https://www.ncbi.nlm.nih.gov/pubmed/23869280
http://dx.doi.org/10.4103/2152-7806.113357
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author Esquenazi, Yoshua
Kerr, Keith
Bhattacharjee, Meenakshi B.
Tandon, Nitin
author_facet Esquenazi, Yoshua
Kerr, Keith
Bhattacharjee, Meenakshi B.
Tandon, Nitin
author_sort Esquenazi, Yoshua
collection PubMed
description BACKGROUND: Dermoid tumors are benign congenital cystic lesions that usually present with local mass effect. Very rarely, they present as spontaneous ruptures. Traumatic rupture of these dermoid cysts is an extremely rare event and only a handful of such cases have been ever reported. CASE DESCRIPTION: A 47-year-old female presented to our hospital with a ruptured intracranial dermoid cyst following a mild head injury. The ruptured cyst contents were disseminated into the subarachnoid and intraventricular compartments, resulting in an obstructive hydrocephalus. After medical stabilization, she underwent gross total resection of the cyst using combined transsylvian, transcortical-transventricular, and sub-frontal approaches. A ventriculo-peritoneal shunt was eventually also needed. CONCLUSION: Traumatic rupture of an intracranial dermoid cyst is an extremely rare event and this is only the fourth such case reported in the literature. We presume that this rupture occurs due to sudden shifts in the cyst sac, which is adherent to some partially mobile intracranial contents. Although computed tomography (CT) is often adequate in making a diagnosis of this entity, magnetic resonance imaging (MRI) provides complete characterization of the extent of lipid dissemination, and is essential for operative planning. Intravenous steroids at presentation are helpful in managing the aseptic meningitis associated with rupture. Complete surgical resection is the goal, but must be weighed against the risk for injury to nearby vital structures. Hydrocephalus should be managed promptly, and patients should be monitored for it closely in the perioperative period. Even though the recurrence rate with subtotal resection is extremely rare, follow up should be done routinely.
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spelling pubmed-37073262013-07-18 Traumatic rupture of an intracranial dermoid cyst: Case report and literature review Esquenazi, Yoshua Kerr, Keith Bhattacharjee, Meenakshi B. Tandon, Nitin Surg Neurol Int Case Report BACKGROUND: Dermoid tumors are benign congenital cystic lesions that usually present with local mass effect. Very rarely, they present as spontaneous ruptures. Traumatic rupture of these dermoid cysts is an extremely rare event and only a handful of such cases have been ever reported. CASE DESCRIPTION: A 47-year-old female presented to our hospital with a ruptured intracranial dermoid cyst following a mild head injury. The ruptured cyst contents were disseminated into the subarachnoid and intraventricular compartments, resulting in an obstructive hydrocephalus. After medical stabilization, she underwent gross total resection of the cyst using combined transsylvian, transcortical-transventricular, and sub-frontal approaches. A ventriculo-peritoneal shunt was eventually also needed. CONCLUSION: Traumatic rupture of an intracranial dermoid cyst is an extremely rare event and this is only the fourth such case reported in the literature. We presume that this rupture occurs due to sudden shifts in the cyst sac, which is adherent to some partially mobile intracranial contents. Although computed tomography (CT) is often adequate in making a diagnosis of this entity, magnetic resonance imaging (MRI) provides complete characterization of the extent of lipid dissemination, and is essential for operative planning. Intravenous steroids at presentation are helpful in managing the aseptic meningitis associated with rupture. Complete surgical resection is the goal, but must be weighed against the risk for injury to nearby vital structures. Hydrocephalus should be managed promptly, and patients should be monitored for it closely in the perioperative period. Even though the recurrence rate with subtotal resection is extremely rare, follow up should be done routinely. Medknow Publications & Media Pvt Ltd 2013-06-12 /pmc/articles/PMC3707326/ /pubmed/23869280 http://dx.doi.org/10.4103/2152-7806.113357 Text en Copyright: © 2013 Esquenazi Y http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Esquenazi, Yoshua
Kerr, Keith
Bhattacharjee, Meenakshi B.
Tandon, Nitin
Traumatic rupture of an intracranial dermoid cyst: Case report and literature review
title Traumatic rupture of an intracranial dermoid cyst: Case report and literature review
title_full Traumatic rupture of an intracranial dermoid cyst: Case report and literature review
title_fullStr Traumatic rupture of an intracranial dermoid cyst: Case report and literature review
title_full_unstemmed Traumatic rupture of an intracranial dermoid cyst: Case report and literature review
title_short Traumatic rupture of an intracranial dermoid cyst: Case report and literature review
title_sort traumatic rupture of an intracranial dermoid cyst: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707326/
https://www.ncbi.nlm.nih.gov/pubmed/23869280
http://dx.doi.org/10.4103/2152-7806.113357
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