Evidence map›Paper›PMID 17377740›Full record

ReviewJournal of neuro-oncology2007

Atypical teratoid/rhabdoid tumor of the spine in an adult: case report and review of the literature.

Elena L Zarovnaya, Henry F Pallatroni, Eugen B Hug, Perry A Ball, Laurence D Cromwell, J Marc Pipas, Camilo E Fadul, Louise P Meyer, Jonathan P Park, Jaclyn A Biegel and 2 more

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Journal of neuro-oncology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
1.7field-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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Spinal atypical teratoid rhabdoid tumor-narrative review and report of a rare case managed with multimodality approach.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Review
  7. Article
  8. Article
  9. Primary atypical teratoid rhabdoid tumor in the adult spine.Surgical neurology international · 2017
    Article
  10. Article
  11. Article
  12. Multifocal atypical teratoid/rhabdoid tumor: a rare entity.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2016
    Article
  13. Article
  14. Atypical teratoid rhabdoid tumour of the spine: report of a case and literature review.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2015
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

12 authors at 5 institutions in 2 countries.

Elena L ZarovnayaDepartment of Pathology, Dartmouth-Hitchcock Medical Center, One Medical Center Drive, Lebanon, NH 03756, USA.
Henry F Pallatroni
Eugen B Hug
Perry A Ball
Laurence D Cromwell
J Marc Pipas
Camilo E Fadul
Louise P Meyer
Jonathan P Park
Jaclyn A Biegel
Arie Perry
C Harker Rhodes
Dartmouth–Hitchcock Medical Center · USChildren's Hospital of Philadelphia · USNaval Medical Center San Diego · USUniversity of Zurich · CHWashington University in St. Louis · US

Funding

MOLECULAR CYTOGENETICS: PEDIATRIC CNS TUMORSR01CA046274 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI BIEGEL, JACLYN A · 1989 to 2012
$2.7M
NCI NIH HHS CA46274
6 · The paper itself

Abstract

Atypical teratoid/rhabdoid tumors (AT/RTs) are rare, malignant brain tumors which occur almost exclusively in infants and young children. There have been only 17 cases of AT/RT in adults reported in the medical literature and the rarity of this tumor makes the diagnosis in adults difficult. We describe a case of an AT/RT of the spinal cord in an adult. A 43-year old woman presented with neck and left upper extremity pain. An MRI demonstrated a mass lesion in the dorsal spinal cord extending from C4 to C6. The patient underwent a C3 through C7 laminectomy. In consultation with senior pathologists at other institutions, the lesion was initially diagnosed as a rhabdoid meningioma. Molecular genetic studies revealed monosomy 22 and loss of expression of the INI1 gene in 22q11.2. Subsequently, immunohistochemical studies revealed the absence of INI1 gene expression in the malignant cells, supporting the diagnosis of AT/RT. The patient underwent three additional surgical procedures for recurrent disease throughout the neuraxis secondary to leptomeningeal spread of the tumor. Despite aggressive surgical resection, adjuvant chemotherapy and radiation therapy, the patient succumbed to the disease two and a half years after her initial presentation. An unrestricted autopsy was performed. To our knowledge, this is the first case of a spinal atypical teratoid/rhabdoid tumor in an adult fully documented with molecular, immunohistochemical, cytogenetic and autopsy findings.

Indexed as

AdultCervical VertebraeChromosomal Proteins, Non-HistoneChromosomes, Human, Pair 22Diagnosis, DifferentialDNA-Binding ProteinsFatal OutcomeFemaleHumansImmunohistochemistryMonosomyNeoplasm Recurrence, LocalRhabdoid TumorSMARCB1 ProteinSpinal Cord NeoplasmsTeratomaChromosomal Proteins, Non-HistoneDNA-Binding ProteinsSMARCB1 ProteinSMARCB1 protein, humanTranscription Factors

Identifiers

PMID17377740
OpenAlexW2010056698

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.