Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome

Background: Spinal hamartoma is an extremely rare lesion for symptomatic spinal cord compression in adult population. Without any association of spinal dysraphism and neurofibromatosis, only 3 cases have been reported in the literature. Case description: A 40-year-old man presented with lumbago femo...

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Autores principales:	Nazmin Ahmed, Shahidul Khan, KM Tarikul Islam, Avijit Dey, Vishal Chavda, Ottavio Tomasi, Gianluca Scalia, Giuseppe E. Umana, Bipin Chaurasia
Formato:	article
Lenguaje:	EN
Publicado:	Al-Azhar University, Faculty of Medicine (Damietta) 2021
Materias:	hamartoma neurofibromatosis spinal dysraphism Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/25dd1a45dcb34951b26a7ce65e14309d
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spelling	oai:doaj.org-article:25dd1a45dcb34951b26a7ce65e14309d2021-12-02T19:02:51ZAdult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome2636-41742682-378010.21608/ijma.2021.66305.1279https://doaj.org/article/25dd1a45dcb34951b26a7ce65e14309d2021-07-01T00:00:00Zhttps://ijma.journals.ekb.eg/article_160652_7a0bbe9d7c5cd1a6ecf9cc5edd7e61b0.pdfhttps://doaj.org/toc/2636-4174https://doaj.org/toc/2682-3780Background: Spinal hamartoma is an extremely rare lesion for symptomatic spinal cord compression in adult population. Without any association of spinal dysraphism and neurofibromatosis, only 3 cases have been reported in the literature. Case description: A 40-year-old man presented with lumbago femorica for 6 months. Gradually the symptoms worsened and he developed features of Cauda equina syndrome. Magnetic Resonence Imagimg demonstrated a heterogeneously hyperintense intradural extramedullary mass in both T1 and T2WI, involving conus medullaris and cauda equina, opposite to L1. Patient underwent near total resection of lesion through posterior midline approach. Histopathological features were consistent with hamartoma. Patient neurologically improved and follow up MRI at 6 months showed static small nodular tumor residue. Conclusion: To the best of our knowledge, current report is the fourth case of spinal hamartoma in adult male, without any association of spinal dysraphism and neurofibromatosis .This may be the first reported case from Bangladesh.Nazmin AhmedShahidul KhanKM Tarikul IslamAvijit DeyVishal ChavdaOttavio TomasiGianluca ScaliaGiuseppe E. UmanaBipin ChaurasiaAl-Azhar University, Faculty of Medicine (Damietta)articlehamartomaneurofibromatosisspinal dysraphismMedicine (General)R5-920ENInternational Journal of Medical Arts, Vol 3, Iss 3, Pp 1556-1561 (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	hamartoma neurofibromatosis spinal dysraphism Medicine (General) R5-920
spellingShingle	hamartoma neurofibromatosis spinal dysraphism Medicine (General) R5-920 Nazmin Ahmed Shahidul Khan KM Tarikul Islam Avijit Dey Vishal Chavda Ottavio Tomasi Gianluca Scalia Giuseppe E. Umana Bipin Chaurasia Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome
description	Background: Spinal hamartoma is an extremely rare lesion for symptomatic spinal cord compression in adult population. Without any association of spinal dysraphism and neurofibromatosis, only 3 cases have been reported in the literature. Case description: A 40-year-old man presented with lumbago femorica for 6 months. Gradually the symptoms worsened and he developed features of Cauda equina syndrome. Magnetic Resonence Imagimg demonstrated a heterogeneously hyperintense intradural extramedullary mass in both T1 and T2WI, involving conus medullaris and cauda equina, opposite to L1. Patient underwent near total resection of lesion through posterior midline approach. Histopathological features were consistent with hamartoma. Patient neurologically improved and follow up MRI at 6 months showed static small nodular tumor residue. Conclusion: To the best of our knowledge, current report is the fourth case of spinal hamartoma in adult male, without any association of spinal dysraphism and neurofibromatosis .This may be the first reported case from Bangladesh.
format	article
author	Nazmin Ahmed Shahidul Khan KM Tarikul Islam Avijit Dey Vishal Chavda Ottavio Tomasi Gianluca Scalia Giuseppe E. Umana Bipin Chaurasia
author_facet	Nazmin Ahmed Shahidul Khan KM Tarikul Islam Avijit Dey Vishal Chavda Ottavio Tomasi Gianluca Scalia Giuseppe E. Umana Bipin Chaurasia
author_sort	Nazmin Ahmed
title	Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome
title_short	Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome
title_full	Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome
title_fullStr	Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome
title_full_unstemmed	Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome
title_sort	adult spinal hamartoma involving conus medullaris: brief review about associated congenital abnormalities and surgical outcome
publisher	Al-Azhar University, Faculty of Medicine (Damietta)
publishDate	2021
url	https://doaj.org/article/25dd1a45dcb34951b26a7ce65e14309d
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Adult Spinal Hamartoma Involving Conus Medullaris: Brief Review About Associated Congenital Abnormalities and Surgical Outcome

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