Evidence map›Paper›PMID 32322332›Full record

ArticleRadiology case reports2020

Unexpected discovery of a diffuse astrocytoma of the conus medullaris in an elderly NF1 patient.

Takamistu Uchi, Tsutomu Inaoka, Noriko Kitamura, Rumiko Ishikawa, Tomoya Nakatsuka, Shusuke Kasuya, Wataru Tokuyama, Nobuyuki Hiruta, Hiroshi Takahashi, Hitoshi Terada

Open access · goldAbstract readCase Reports
In one paragraph

Article in Radiology case reports, 2020. 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
0.2field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Spinal manifestations of Neurofibromatosis type 1.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Review
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

10 authors at 1 institution in 1 country.

Takamistu UchiDepartment of Radiology, Toho University Sakura Medical Center.
Tsutomu InaokaDepartment of Radiology, Toho University Sakura Medical Center.
Noriko KitamuraDepartment of Radiology, Toho University Sakura Medical Center.
Rumiko IshikawaDepartment of Radiology, Toho University Sakura Medical Center.
Tomoya NakatsukaDepartment of Radiology, Toho University Sakura Medical Center.
Shusuke KasuyaDepartment of Radiology, Toho University Sakura Medical Center.
Wataru TokuyamaDivision of Surgical Pathology, Toho University Sakura Medical Center.
Nobuyuki HirutaDivision of Surgical Pathology, Toho University Sakura Medical Center.
Hiroshi TakahashiDepartment of Orthopedic Surgery, Toho University Sakura Medical Center.
Hitoshi TeradaDepartment of Radiology, Toho University Sakura Medical Center.
Toho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is one of the most common genetic neurocutaneous disorders, and it is well known to be associated with peripheral or central nervous system malignancies. The most common malignant tumors are malignant peripheral nerve sheath tumors (MPNSTs); MPNSTs are the most common cause of death in patients with NF1. Central nervous system malignancies rarely occur. So far, the occurrence of spinal cord malignancies is exceedingly rare. Herein, we report a rare case of a 69-year-old male with NF1 following tumor resection twice for cutaneous MPNSTs developing intramedullary diffuse astrocytoma in the conus medullaris, which initially presented with traumatic spinal cord injury associated with a compression fracture from fall. Contrast-enhanced magnetic resonance imaging and biopsy of the spinal cord were required to establish the final diagnosis.

Indexed as

BiopsyDiffuse astrocytomaFollow-up MRINeurofibromatosisSpinal cord

Identifiers

PMID32322332
PMCPMC7167499
OpenAlexW3016557360

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.