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Ruptured Tentorium Originating Masson Tumor

Intravascular papillary endothelial hyperplasia (IPEH) also known as Masson's tumor, is a benign, slow growing, vascular lesion which is seen very rarely and only a few cases have been reported intracranially in the literature. It has been reported at many sites, but the posterior fossa involve...

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Autores principales: Sekmen, Haydar, Doğan, Ihsan, Mammadkhanli, Orkhan, Erden, Esra, Tuna, Hakan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202391/
https://www.ncbi.nlm.nih.gov/pubmed/34211895
http://dx.doi.org/10.4103/ajns.AJNS_249_20
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author Sekmen, Haydar
Doğan, Ihsan
Mammadkhanli, Orkhan
Erden, Esra
Tuna, Hakan
author_facet Sekmen, Haydar
Doğan, Ihsan
Mammadkhanli, Orkhan
Erden, Esra
Tuna, Hakan
author_sort Sekmen, Haydar
collection PubMed
description Intravascular papillary endothelial hyperplasia (IPEH) also known as Masson's tumor, is a benign, slow growing, vascular lesion which is seen very rarely and only a few cases have been reported intracranially in the literature. It has been reported at many sites, but the posterior fossa involvement is very rare. The preoperative diagnosis is very difficult, as there is no enough cases to achieve a clear understanding about the details of its radiological findings. Differential diagnosis have to be made especially from angiosarcoma and meningioma. It is curable by total surgical removal. In this article we presented the characteristic clinical, radiological, perioperative and pathological findings in a case of IPEH in an unusual location, origin and behavior. To best of our knowledge, we presented the first case of IPEH originating from tentorium.
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spelling pubmed-82023912021-06-30 Ruptured Tentorium Originating Masson Tumor Sekmen, Haydar Doğan, Ihsan Mammadkhanli, Orkhan Erden, Esra Tuna, Hakan Asian J Neurosurg Case Report Intravascular papillary endothelial hyperplasia (IPEH) also known as Masson's tumor, is a benign, slow growing, vascular lesion which is seen very rarely and only a few cases have been reported intracranially in the literature. It has been reported at many sites, but the posterior fossa involvement is very rare. The preoperative diagnosis is very difficult, as there is no enough cases to achieve a clear understanding about the details of its radiological findings. Differential diagnosis have to be made especially from angiosarcoma and meningioma. It is curable by total surgical removal. In this article we presented the characteristic clinical, radiological, perioperative and pathological findings in a case of IPEH in an unusual location, origin and behavior. To best of our knowledge, we presented the first case of IPEH originating from tentorium. Wolters Kluwer - Medknow 2021-02-23 /pmc/articles/PMC8202391/ /pubmed/34211895 http://dx.doi.org/10.4103/ajns.AJNS_249_20 Text en Copyright: © 2021 Asian Journal of Neurosurgery https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Sekmen, Haydar
Doğan, Ihsan
Mammadkhanli, Orkhan
Erden, Esra
Tuna, Hakan
Ruptured Tentorium Originating Masson Tumor
title Ruptured Tentorium Originating Masson Tumor
title_full Ruptured Tentorium Originating Masson Tumor
title_fullStr Ruptured Tentorium Originating Masson Tumor
title_full_unstemmed Ruptured Tentorium Originating Masson Tumor
title_short Ruptured Tentorium Originating Masson Tumor
title_sort ruptured tentorium originating masson tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202391/
https://www.ncbi.nlm.nih.gov/pubmed/34211895
http://dx.doi.org/10.4103/ajns.AJNS_249_20
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