Evidence map›Paper›PMID 35687168›Full record

SynthesisChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2022

Split cord malformation concomitant with spinal teratoma without open spinal dysraphism.

Jülide Hazneci, Feryal Bastacı, Ali Börekci, Özden Çağlar Öztürk, Merih İş, Adnan Somay, Murat Şakir Ekşi, Erhan Çelikoğlu

Abstract readCase ReportsSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2022. 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
0.6field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Prenatal diagnosis of meningomyelocele resolves as a mature cystic teratoma in the thoracolumbar region.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Article
  3. 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

8 authors at 3 institutions in 2 countries.

Jülide HazneciFSM Training and Research Hospital, Neurosurgery Clinic, Istanbul, Turkey.
Feryal BastacıFSM Training and Research Hospital, Neurosurgery Clinic, Istanbul, Turkey.
Ali BörekciFSM Training and Research Hospital, Neurosurgery Clinic, Istanbul, Turkey.
Özden Çağlar ÖztürkFSM Training and Research Hospital, Neurosurgery Clinic, Istanbul, Turkey.
Merih İşPrivate Practice, Neurosurgery, Istanbul, Turkey.
Adnan SomayFSM Training and Research Hospital, Pathology Clinic, Istanbul, Turkey.
Murat Şakir EkşiFSM Training and Research Hospital, Neurosurgery Clinic, Istanbul, Turkey. muratsakireksi@gmail.com.ORCID http://orcid.org/0000-0002-3036-0061
Erhan ÇelikoğluFSM Training and Research Hospital, Neurosurgery Clinic, Istanbul, Turkey.
Ministry of Health · TRTurkish Society of Hematology · TRYeditepe University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSplit cord malformation (SCM) presenting concomitant with spinal teratoma without any open spinal dysraphism has rarely been reported in the literature. We aimed to make a systematic review and qualitative analysis of the literature about the topic and present the first case of SCM concomitant with spinal teratoma harboring papillary thyroid carcinoma (PTC) component.

methodsTwo big search tools (Pubmed/MEDLINE) and Scopus were used. The search strategy was compatible to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). An exemplary case of ours was also presented.

resultsThere were 30 patients (15 pediatric and 15 adult). Female and male distribution was even. Median age of the patients was 18 years (range = 0-66 years). The most common presenting symptoms were back pain and lower limb weakness. Spinal teratoma and SCM mostly presented at thoracic/thoracolumbar region in children and lumbar region in adults. Surgical outcome was better in the children compared to the adults.

conclusionThoracolumbar region is the most common location for such entity in children, whereas lumbar region for the adults. Surgical resection should be done as much as possible under neuromonitorization. The resected material should be evaluated thoroughly not to miss any malign pathology. Surgical outcome is better when it is done at an early age.

Indexed as

Neural Tube DefectsSpinal DysraphismTeratomaAdolescentAdultAgedChildChild, PreschoolFemaleHumansInfantInfant, NewbornMagnetic Resonance ImagingMaleMiddle AgedMuscle WeaknessDiastematomyeliaSpinal teratomaSplit cord malformation

Identifiers

PMID35687168
OpenAlexW4281635646

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.