Evidence map›Paper›PMID 39133940›Full record

ArticleJournal of neurosurgery. Case lessons2024

Pediatric atypical teratoid/rhabdoid tumor in the cauda equina with rapid tumor progression: illustrative case.

Takahiro Tsuchiya, Makoto Ohno, Yuko Watanabe, Shohei Fujita, Bunpei Miyazaki, Hirokazu Sugino, Hiroshi Igaki, Akihiko Yoshida, Masamichi Takahashi, Shunsuke Yanagisawa and 3 more

Abstract read
In one paragraph

Article in Journal of neurosurgery. Case lessons, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Takahiro TsuchiyaDepartments of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo, Japan.
Makoto OhnoDepartments of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yuko WatanabeDepartments of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
Shohei FujitaDepartments of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo, Japan.
Bunpei MiyazakiDepartments of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
Hirokazu SuginoDepartments of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
Hiroshi IgakiDepartments of Radiation Oncology, National Cancer Center Hospital, Tokyo, Japan.
Akihiko YoshidaDepartments of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
Masamichi TakahashiDepartments of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo, Japan.
Shunsuke YanagisawaDepartments of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo, Japan.
Sho OsawaDepartments of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo, Japan.
Chitose OgawaDepartments of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yoshitaka NaritaDepartments of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtypical teratoid/rhabdoid tumor (AT/RT) is an uncommon malignant neoplasm and rarely occurs in the spinal space, especially in the cauda equina. Only 8 cases of pediatric AT/RT of the cauda equina have been reported. Therefore, its clinical behavior and optimal treatment remain unclear. OBSERVATIONS: The authors describe the case of a 9-year-old boy who presented with progressive back and left leg pain. Initial magnetic resonance imaging showed an intradural extramedullary lesion at the L3-4 level, which progressed rapidly to the L2-5 level within a month. He underwent partial resection of the tumor with an L2-5 laminectomy. The histopathological diagnosis was AT/RT. He received adjuvant chemotherapy and radiotherapy, and his gait disturbance improved postoperatively. At 6 months' follow-up, disease recurrence was not observed. LESSONS: Although extremely rare, AT/RT should be included in the differential diagnosis for prompt therapeutic intervention. Safe resection with minimal functional impairment, followed by postoperative chemoradiation, can lead to tumor control and improve neurological function. https://thejns.org/doi/10.3171/CASE24219.

Indexed as

atypical teratoid/rhabdoid tumorcase reportcauda equinapediatricspinal

Identifiers

PMID39133940
PMCPMC11323848

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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.