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Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst

We describe a rare case of 42-year-old female who had possible double crush syndrome caused by iatrogenic spinal epidermoid tumor (ET) associated with lumbar puncture as well as concomitant sacral Tarlov cyst in close proximity. She presented with progressive left-sided perianal pain. She had a hist...

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Autores principales: Nishimura, Yusuke, Hara, Masahito, Awaya, Takayuki, Ando, Ryo, Eguchi, Kaoru, Nagashima, Yoshitaka, Wakabayashi, Toshihiko, Ginsberg, Howard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538451/
https://www.ncbi.nlm.nih.gov/pubmed/33062568
http://dx.doi.org/10.2176/nmccrj.cr.2019-0236
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author Nishimura, Yusuke
Hara, Masahito
Awaya, Takayuki
Ando, Ryo
Eguchi, Kaoru
Nagashima, Yoshitaka
Wakabayashi, Toshihiko
Ginsberg, Howard J.
author_facet Nishimura, Yusuke
Hara, Masahito
Awaya, Takayuki
Ando, Ryo
Eguchi, Kaoru
Nagashima, Yoshitaka
Wakabayashi, Toshihiko
Ginsberg, Howard J.
author_sort Nishimura, Yusuke
collection PubMed
description We describe a rare case of 42-year-old female who had possible double crush syndrome caused by iatrogenic spinal epidermoid tumor (ET) associated with lumbar puncture as well as concomitant sacral Tarlov cyst in close proximity. She presented with progressive left-sided perianal pain. She had a history of a Caesarean section with lumbar spinal anesthesia. Magnetic resonance imaging (MRI) demonstrated a relatively small intradural extramedullary solid lesion at L5/S1 level and cystic lesion at S2 level. We considered there were two different lesions, such as a tumor and Tarlov cyst; however, we could not rule out the possibility of a single lesion with two different components. Furthermore, there was a distinct compression at more than one locations along the course of the left S2 nerve root and we suspected possible double crush syndrome. We conducted tumor removal and the lesion turned out to be two different pathologies, such as an ET and Tarlov cyst. Both lesions were intraopertively pinching the left S2 nerve root at different sites as expected. The tumor was successfully removed and the cyst wall was imbricated and sutured. We need to take the possibility of ET into consideration if the patient underwent invasive spinal procedure previously. We also have to pay attention to the possibility of double crush syndrome if the nerve root possibly holding the responsibility for symptoms is compressed at two or more sites. This is the first report of possible double crush syndrome caused by acquired spinal tumor and congenital Tarlov cyst.
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spelling pubmed-75384512020-10-13 Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst Nishimura, Yusuke Hara, Masahito Awaya, Takayuki Ando, Ryo Eguchi, Kaoru Nagashima, Yoshitaka Wakabayashi, Toshihiko Ginsberg, Howard J. NMC Case Rep J Case Report We describe a rare case of 42-year-old female who had possible double crush syndrome caused by iatrogenic spinal epidermoid tumor (ET) associated with lumbar puncture as well as concomitant sacral Tarlov cyst in close proximity. She presented with progressive left-sided perianal pain. She had a history of a Caesarean section with lumbar spinal anesthesia. Magnetic resonance imaging (MRI) demonstrated a relatively small intradural extramedullary solid lesion at L5/S1 level and cystic lesion at S2 level. We considered there were two different lesions, such as a tumor and Tarlov cyst; however, we could not rule out the possibility of a single lesion with two different components. Furthermore, there was a distinct compression at more than one locations along the course of the left S2 nerve root and we suspected possible double crush syndrome. We conducted tumor removal and the lesion turned out to be two different pathologies, such as an ET and Tarlov cyst. Both lesions were intraopertively pinching the left S2 nerve root at different sites as expected. The tumor was successfully removed and the cyst wall was imbricated and sutured. We need to take the possibility of ET into consideration if the patient underwent invasive spinal procedure previously. We also have to pay attention to the possibility of double crush syndrome if the nerve root possibly holding the responsibility for symptoms is compressed at two or more sites. This is the first report of possible double crush syndrome caused by acquired spinal tumor and congenital Tarlov cyst. The Japan Neurosurgical Society 2020-09-15 /pmc/articles/PMC7538451/ /pubmed/33062568 http://dx.doi.org/10.2176/nmccrj.cr.2019-0236 Text en © 2020 The Japan Neurosurgical Society This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Case Report
Nishimura, Yusuke
Hara, Masahito
Awaya, Takayuki
Ando, Ryo
Eguchi, Kaoru
Nagashima, Yoshitaka
Wakabayashi, Toshihiko
Ginsberg, Howard J.
Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst
title Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst
title_full Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst
title_fullStr Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst
title_full_unstemmed Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst
title_short Possible Double Crush Syndrome Caused by Iatrogenic Acquired Lumbosacral Epidermoid Tumor and Concomitant Sacral Tarlov Cyst
title_sort possible double crush syndrome caused by iatrogenic acquired lumbosacral epidermoid tumor and concomitant sacral tarlov cyst
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538451/
https://www.ncbi.nlm.nih.gov/pubmed/33062568
http://dx.doi.org/10.2176/nmccrj.cr.2019-0236
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