Evidence map›Paper›PMID 34513140›Full record

ArticleSurgical neurology international2021

Surgical histopathology of a filar anomaly as an additional tethering element associated with closed spinal dysraphism of primary neurulation failure.

Takato Morioka, Nobuya Murakami, Satoshi O Suzuki, Nobutaka Mukae, Takafumi Shimogawa, Ai Kurogi, Tadahisa Shono, Masahiro Mizoguchi

Open access · hybridAbstract read
In one paragraph

Article in Surgical neurology international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Diagnosis and Management of Tethered Cord Syndrome.Advances and technical standards in neurosurgery · 2024
    Article
  3. Article
  4. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Takato MoriokaDepartment of Neurosurgery, Fukuoka Children's Hospital, Fukuoka, Japan.
Nobuya MurakamiDepartment of Neurosurgery, Fukuoka Children's Hospital, Fukuoka, Japan.
Satoshi O SuzukiDepartment of Psychiatry, Shourai Hospital, Karatsu, Saga.
Nobutaka MukaeDepartment of Neurosurgery, Graduate School of Medical Sciences, Fukuoka, Japan.
Takafumi ShimogawaDepartment of Neurosurgery, Kyushu University, Fukuoka, Fukuoka, Japan.
Ai KurogiDepartment of Neurosurgery, Fukuoka Children's Hospital, Fukuoka, Japan.
Tadahisa ShonoDepartment of Neurosurgery, Harasanshin Hospital, Karatsu, Saga.
Masahiro MizoguchiDepartment of Neurosurgery, Graduate School of Medical Sciences, Fukuoka, Japan.
Fukuoka Children's Hospital and Medical Center for Infectious Diseases · JPHarasanshin Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClosed spinal dysraphism of primary neurulation failure could be associated with filar anomalies, such as filar lipoma or thickened and tight filum terminale (TFT), resulting from impaired secondary neurulation. Retained medullary cord (RMC) is a remnant of the cavitary medullary cord originating from the secondary neurulation failure. Some filar lipomas are known to contain a central canal-like ependyma-lined lumen with surrounding neuroglial tissues (E-LC w/NGT), that is, a characteristic histopathology of RMC. To clarify the embryological background of these filar anomalies, we evaluated the histopathological findings.

methodsAmong 41 patients with lesions of primary neurulation failure who underwent initial untethering surgery, the filum including cord-like structure (C-LS) was additionally resected in 10 patients (five dorsal and transitional lipomas; five limited dorsal myeloschisis). We retrospectively analyzed the clinical, neuroradiological, intraoperative, and histopathological findings.

resultsAmong 10 patients, two patients were diagnosed with RMC based on morphological features and intraoperative neurophysiological monitoring. The diagnosis of filar lipoma was made in six patients, since various amounts of fibroadipose tissue were histopathologically noted in the filum. Two patients were diagnosed with TFT, since the filum was composed solely of fibrocollagenous tissue. E-LC w/NGT was noted not only in both C-LSs of RMCs but also in two out of six fila both with filar lipomas and fila with TFTs.

conclusionThese findings provide further evidence for the idea that entities, such as filar lipoma, TFT, and RMC, can be considered consequences of a continuum of regression failure occurring during late secondary neurulation.

Indexed as

Central canalEpendymaFilar type lipomaNeuroglial corePrimary neurulationRetained medullary cordSecondary neurulation

Identifiers

PMID34513140
PMCPMC8422463
OpenAlexW3186082559

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.