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Lipofibromatous hamartoma of the median nerve

Lipofibromatous hamartoma is a rare tumour of peripheral nerves which is characterised by an excessive infiltration of the epineurium and perineurium by fibroadipose tissue. To the best of our knowledge, only approximately 88 cases are reported in the literature. We report a rare case of lipofibroma...

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Autores principales: Al-Jabri, Talal, Garg, Sunil, Mani, Ganapathyraman V
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955673/
https://www.ncbi.nlm.nih.gov/pubmed/20920178
http://dx.doi.org/10.1186/1749-799X-5-71
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author Al-Jabri, Talal
Garg, Sunil
Mani, Ganapathyraman V
author_facet Al-Jabri, Talal
Garg, Sunil
Mani, Ganapathyraman V
author_sort Al-Jabri, Talal
collection PubMed
description Lipofibromatous hamartoma is a rare tumour of peripheral nerves which is characterised by an excessive infiltration of the epineurium and perineurium by fibroadipose tissue. To the best of our knowledge, only approximately 88 cases are reported in the literature. We report a rare case of lipofibromatous hamartoma of the median nerve causing secondary carpal tunnel syndrome in a 25 year old patient. This patient was treated conservatively with decompression and biopsy and experienced a complete resolution of symptoms post-operatively. Magnetic resonance imaging may be used to diagnose this lesion as it has very distinctive characteristics. Multiple conditions have been associated with this lesion and a greater understanding of these associations may clarify the pathogenesis. The architecture of the tumour makes excision very challenging and the surgical management remains controversial. A review of the literature regarding the etiology, pathogenesis and surgical management of lipofibromatous hamartoma is included.
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spelling pubmed-29556732010-10-16 Lipofibromatous hamartoma of the median nerve Al-Jabri, Talal Garg, Sunil Mani, Ganapathyraman V J Orthop Surg Res Review Lipofibromatous hamartoma is a rare tumour of peripheral nerves which is characterised by an excessive infiltration of the epineurium and perineurium by fibroadipose tissue. To the best of our knowledge, only approximately 88 cases are reported in the literature. We report a rare case of lipofibromatous hamartoma of the median nerve causing secondary carpal tunnel syndrome in a 25 year old patient. This patient was treated conservatively with decompression and biopsy and experienced a complete resolution of symptoms post-operatively. Magnetic resonance imaging may be used to diagnose this lesion as it has very distinctive characteristics. Multiple conditions have been associated with this lesion and a greater understanding of these associations may clarify the pathogenesis. The architecture of the tumour makes excision very challenging and the surgical management remains controversial. A review of the literature regarding the etiology, pathogenesis and surgical management of lipofibromatous hamartoma is included. BioMed Central 2010-09-28 /pmc/articles/PMC2955673/ /pubmed/20920178 http://dx.doi.org/10.1186/1749-799X-5-71 Text en Copyright ©2010 Al-Jabri et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Al-Jabri, Talal
Garg, Sunil
Mani, Ganapathyraman V
Lipofibromatous hamartoma of the median nerve
title Lipofibromatous hamartoma of the median nerve
title_full Lipofibromatous hamartoma of the median nerve
title_fullStr Lipofibromatous hamartoma of the median nerve
title_full_unstemmed Lipofibromatous hamartoma of the median nerve
title_short Lipofibromatous hamartoma of the median nerve
title_sort lipofibromatous hamartoma of the median nerve
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955673/
https://www.ncbi.nlm.nih.gov/pubmed/20920178
http://dx.doi.org/10.1186/1749-799X-5-71
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