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Spinal intradural subpial angiolipoma: Case report and review of literature

BACKGROUND: Spinal angiolipomas are rare tumors consisting of mature adipose tissue and abnormal vascular elements. Intradural location is very rare, and till now, only seven cases have been reported in literature. Authors report a case of an intradural intramedullary (subpial) angiolipoma located i...

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Detalles Bibliográficos
Autores principales: Prasad, G. Lakshmi, Sinha, Sumit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278084/
https://www.ncbi.nlm.nih.gov/pubmed/25558423
http://dx.doi.org/10.4103/2152-7806.145770
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author Prasad, G. Lakshmi
Sinha, Sumit
author_facet Prasad, G. Lakshmi
Sinha, Sumit
author_sort Prasad, G. Lakshmi
collection PubMed
description BACKGROUND: Spinal angiolipomas are rare tumors consisting of mature adipose tissue and abnormal vascular elements. Intradural location is very rare, and till now, only seven cases have been reported in literature. Authors report a case of an intradural intramedullary (subpial) angiolipoma located in the thoracic cord. CASE DESCRIPTION: A 26-year-old patient presented with features of progressive myelopathy of relatively short duration. Imaging showed a heterogeneous fat-containing intradural lesion at D5-D9 level, which enhanced on contrast enhanced fat saturation sequences. Subtotal excision was performed and patient had partial recovery of his neurological deficits. Histopathology was suggestive of angiolipoma. CONCLUSIONS: Intradural angiolipomas are very rare. Complete excision often leads to neurological deficits. Hence, safe maximal decompression would suffice leading to long-term recurrence-free periods.
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spelling pubmed-42780842015-01-02 Spinal intradural subpial angiolipoma: Case report and review of literature Prasad, G. Lakshmi Sinha, Sumit Surg Neurol Int Case Report BACKGROUND: Spinal angiolipomas are rare tumors consisting of mature adipose tissue and abnormal vascular elements. Intradural location is very rare, and till now, only seven cases have been reported in literature. Authors report a case of an intradural intramedullary (subpial) angiolipoma located in the thoracic cord. CASE DESCRIPTION: A 26-year-old patient presented with features of progressive myelopathy of relatively short duration. Imaging showed a heterogeneous fat-containing intradural lesion at D5-D9 level, which enhanced on contrast enhanced fat saturation sequences. Subtotal excision was performed and patient had partial recovery of his neurological deficits. Histopathology was suggestive of angiolipoma. CONCLUSIONS: Intradural angiolipomas are very rare. Complete excision often leads to neurological deficits. Hence, safe maximal decompression would suffice leading to long-term recurrence-free periods. Medknow Publications & Media Pvt Ltd 2014-11-28 /pmc/articles/PMC4278084/ /pubmed/25558423 http://dx.doi.org/10.4103/2152-7806.145770 Text en Copyright: © 2014 Prasad GL. 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
Prasad, G. Lakshmi
Sinha, Sumit
Spinal intradural subpial angiolipoma: Case report and review of literature
title Spinal intradural subpial angiolipoma: Case report and review of literature
title_full Spinal intradural subpial angiolipoma: Case report and review of literature
title_fullStr Spinal intradural subpial angiolipoma: Case report and review of literature
title_full_unstemmed Spinal intradural subpial angiolipoma: Case report and review of literature
title_short Spinal intradural subpial angiolipoma: Case report and review of literature
title_sort spinal intradural subpial angiolipoma: case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278084/
https://www.ncbi.nlm.nih.gov/pubmed/25558423
http://dx.doi.org/10.4103/2152-7806.145770
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