Evidence map›Paper›PMID 33730897›Full record

ReviewThe Journal of international medical research2021

Retropharyngeal chordoma extending to the spinal cord, mimicking a neurogenic tumor: a case report and literature review.

Sun Joo Lee, Sung Hwa Paeng, Mi Seon Kang, Soo Jin Jung, Shin Ae Yoon, Ha Young Park, Hye Kyoung Yoon, Young Il Yang, Hwa Jin Cho

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in The Journal of international medical research, 2021. 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
0.7field-weighted citation impact, top 31% 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, 4 citations in OpenAlex.

  1. Article
  2. An Unusual Chordoma of the Odontoid Process: A Case Report and Literature Review.Journal of the American Academy of Orthopaedic Surgeons. Global research & reviews · 2022
    Review
  3. Thoracic dumbbell spinal chordoma mimicking a schwannoma.Surgical neurology international · 2021
    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

9 authors at 2 institutions in 1 country.

Sun Joo LeeDepartment of Radiology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Sung Hwa PaengDepartment of Neurosurgery, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Mi Seon KangDepartment of Pathology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Soo Jin JungDepartment of Pathology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Shin Ae YoonDepartment of Pediatrics, Chungbuk National University Hospital, Cheongju, Chungcheongbuk-do, Republic of Korea.
Ha Young ParkDepartment of Pathology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Hye Kyoung YoonDepartment of Pathology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Young Il YangDepartment of Pathology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Hwa Jin ChoDepartment of Pathology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.ORCID https://orcid.org/0000-0002-7613-1942
Inje University Busan Paik Hospital · KRChungbuk National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chordomas are rare, locally aggressive bone malignancies with poor prognoses. However, those with minimal or no bone involvement are more easily resectable because of their well-delineated margins and thus have better prognoses. Such extraosseous chordomas of the spine are localized both intradurally and extradurally. Only a few case reports have focused on extraosseous, extradural spinal chordomas. Radiologically, this type of chordoma has a dumbbell shape; however, dumbbell-shaped spinal tumors are traditionally thought to be neurogenic tumors (i.e., schwannomas or neurofibromas). We herein report a unique case involving a woman with a dumbbell-shaped extraosseous chordoma protruding predominantly into the retropharyngeal space. A 44-year-old woman presented for evaluation of a left submandibular mass. A T2-hyperintense, gadolinium-enhancing mass was found in her cervical spinal canal, protruding through the C2/3 neural foramen into the retropharyngeal space with minimal vertebral involvement. The initial diagnosis was a neurogenic tumor, most likely a schwannoma. After subtotal removal, the pathologic diagnosis was a chordoma. Because chordomas and schwannomas have significantly different prognoses, caution is warranted when a dumbbell-shaped tumor is identified in the spine with minimal or no vertebral deterioration on radiology. This report also provides the first thorough review of extraosseous dumbbell-shaped intraspinal-extraspinal chordomas.

Indexed as

ChordomaNeurilemmomaSpinal Cord NeoplasmsSpinal NeoplasmsAdultFemaleHumansMagnetic Resonance Imagingcase reportChordomadumbbellextraosseousneurogenic tumorretropharyngeal space

Identifiers

PMID33730897
PMCPMC8166386
OpenAlexW3137701515

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.