Evidence map›Paper›PMID 34473883›Full record

ReviewPathology international2021

A case of an atypical teratoid/rhabdoid tumor with distinctive histology in the pineal region in an adult patient.

Masatomo Doi, Junki Koike, Yasuyuki Yoshida, Hisao Nakamura, Motohiro Chosokabe, Saeko Naruki, Shinya Tajima, Akira Endo, Takashi Matsumori, Yuichiro Tanaka

Open access · hybridAbstract readCase ReportsReview
In one paragraph

Review in Pathology international, 2021. 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 51% 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. 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.

Masatomo DoiDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.ORCID http://orcid.org/0000-0002-8365-7272
Junki KoikeDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Yasuyuki YoshidaDepartment of Neurosurgery, St. Marianna University School of Medicine, Toyoko Hospital, Kawasaki, Kanagawa, Japan.
Hisao NakamuraDepartment of Radiology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Motohiro ChosokabeDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Saeko NarukiDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Shinya TajimaDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Akira EndoDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Takashi MatsumoriDepartment of Neurosurgery, St. Marianna University School of Medicine, Toyoko Hospital, Kawasaki, Kanagawa, Japan.
Yuichiro TanakaDepartment of Neurosurgery, St. Marianna University School of Medicine, Toyoko Hospital, Kawasaki, Kanagawa, Japan.
St. Marianna University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 31-year-old man suffered from headaches and presented at a hospital after the symptom worsened. Obstructive hydrocephalus and a pineal tumor were identified, and he was transferred to our hospital for further investigation and treatment. Cranial computed tomography revealed a hypodense mass lesion on the right of the pineal region, and calcifications and enlargement of the lateral and third cerebral ventricles were also evident. Blood tests were negative for all tumor markers. Laparoscopic biopsy and third-ventricle fenestration were performed that day as an emergency surgery to treat the obstructive hydrocephalus. Postoperative cranial magnetic resonance imaging revealed a solid tumor that was hypointense on T1-weighted imaging, hyperintense on T2-weighted imaging, and heterogeneously enhanced by Gd. Subsequently, the tumor increased in size, and craniotomy and tumorectomy were performed. Histologically, the tumor proliferated as round or short spindle-shaped cells in a myxoid matrix, forming arrays that surrounded the blood vessels. As a few cells with eosinophilic cytoplasm were also present and immunostaining for INI-1 was negative, the patient was diagnosed with atypical teratoid/rhabdoid tumor (AT/RT). AT/RT of the pineal region in adults is rare, and herein, we report the morphological characteristics of this case and reviewed the relevant literature.

Indexed as

AdultBrain NeoplasmsHumansMalePineal GlandRhabdoid TumorTeratomaadultatypical teratoid/rhabdoid tumor (AT/RT)craniotomyheadacheobstructive hydrocephaluspineal region

Identifiers

PMID34473883
PMCPMC9292907
OpenAlexW3196804901

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.