Evidence map›Paper›PMID 33062568›Full record

ArticleNMC case report journal2020

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

Yusuke Nishimura, Masahito Hara, Takayuki Awaya, Ryo Ando, Kaoru Eguchi, Yoshitaka Nagashima, Toshihiko Wakabayashi, Howard J Ginsberg

Abstract readCase Reports
In one paragraph

Article in NMC case report journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yusuke NishimuraDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Masahito HaraDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Takayuki AwayaDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Ryo AndoDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Kaoru EguchiDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Yoshitaka NagashimaDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Toshihiko WakabayashiDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Howard J GinsbergDivision of Neurosurgery, St. Michael's Hospital, University of Toronto, Toronto, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

double crush syndromeepidermoid tumoriatrogenic tumorlumbar punctureTarlov cyst

Identifiers

PMID33062568
PMCPMC7538451

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