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Multiple Meningiomata in Cowden Syndrome

Cowden syndrome (CS) is a rare, congenital disease with associated cancers, but in a neurosurgical context is typically considered part of Lhermitte-Duclos. This misrepresentation is the likely cause of under-diagnosis. Furthermore, the presence of meningiomata has been described in CS patients but...

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Autores principales: Aggarwal, Vishal, Mohmed, AlHassan, Kumaria, Ashwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667626/
https://www.ncbi.nlm.nih.gov/pubmed/33209564
http://dx.doi.org/10.7759/cureus.11469
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author Aggarwal, Vishal
Mohmed, AlHassan
Kumaria, Ashwin
author_facet Aggarwal, Vishal
Mohmed, AlHassan
Kumaria, Ashwin
author_sort Aggarwal, Vishal
collection PubMed
description Cowden syndrome (CS) is a rare, congenital disease with associated cancers, but in a neurosurgical context is typically considered part of Lhermitte-Duclos. This misrepresentation is the likely cause of under-diagnosis. Furthermore, the presence of meningiomata has been described in CS patients but its absence as part of the condition’s major criteria suggest the correlation requires greater documentation. A 41-year-old woman with multiple cancers and a familial circumambience of CS was reviewed in clinic where multiple meningiomata were incidentally identified on MRI. Despite a lack of neurological impairment, and the general reluctance in treating the meningiomas of congenital disease with radiotherapy (RT), the patient underwent stereotactic radio-surgery (SRS) and at one-year post-procedure has reported no side effects or toxicity.
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spelling pubmed-76676262020-11-17 Multiple Meningiomata in Cowden Syndrome Aggarwal, Vishal Mohmed, AlHassan Kumaria, Ashwin Cureus Genetics Cowden syndrome (CS) is a rare, congenital disease with associated cancers, but in a neurosurgical context is typically considered part of Lhermitte-Duclos. This misrepresentation is the likely cause of under-diagnosis. Furthermore, the presence of meningiomata has been described in CS patients but its absence as part of the condition’s major criteria suggest the correlation requires greater documentation. A 41-year-old woman with multiple cancers and a familial circumambience of CS was reviewed in clinic where multiple meningiomata were incidentally identified on MRI. Despite a lack of neurological impairment, and the general reluctance in treating the meningiomas of congenital disease with radiotherapy (RT), the patient underwent stereotactic radio-surgery (SRS) and at one-year post-procedure has reported no side effects or toxicity. Cureus 2020-11-13 /pmc/articles/PMC7667626/ /pubmed/33209564 http://dx.doi.org/10.7759/cureus.11469 Text en Copyright © 2020, Aggarwal et al. http://creativecommons.org/licenses/by/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 Genetics
Aggarwal, Vishal
Mohmed, AlHassan
Kumaria, Ashwin
Multiple Meningiomata in Cowden Syndrome
title Multiple Meningiomata in Cowden Syndrome
title_full Multiple Meningiomata in Cowden Syndrome
title_fullStr Multiple Meningiomata in Cowden Syndrome
title_full_unstemmed Multiple Meningiomata in Cowden Syndrome
title_short Multiple Meningiomata in Cowden Syndrome
title_sort multiple meningiomata in cowden syndrome
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667626/
https://www.ncbi.nlm.nih.gov/pubmed/33209564
http://dx.doi.org/10.7759/cureus.11469
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