Evidence map›Paper›PMID 35846908›Full record

ArticleClinical case reports2022

Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report.

Tahereh Ashraf Ganjooei, Zanbagh Pirastehfar, Asieh Mosallanejad, Masoomeh Raoufi, Noushin Afshar Moghaddam, Mozhgan Hashemieh

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical case reports, 2022. 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
0.3field-weighted citation impact, top 48% 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, 4 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 1 country.

Tahereh Ashraf GanjooeiDepartment of Obstetrics and Gynecology, School of Medicine, Preventative Gynecology Research Center, Imam Hossein Medical Center Shahid Beheshti University of Medical Sciences Tehran Iran.
Zanbagh PirastehfarDepartment of Obstetrics and Gynecology, School of Medicine, Imam Khomeini Hospital Mazandaran University of Medical Sciences Sari Iran.ORCID https://orcid.org/0000-0002-0655-988X
Asieh MosallanejadDepartment of Pediatric Endocrinology & Metabolism, School of Medicine, Imam Hossein Medical Center Shahid Beheshti University of Medical Sciences Tehran Iran.
Masoomeh RaoufiDepartment of Radiology, School of Medicine, Imam Hossein Medical Center Shahid Beheshti University of Medical Sciences Tehran Iran.
Noushin Afshar MoghaddamDepartment of Pathology, School of Medicine, Imam Hossein Medical Center Shahid Beheshti University of Medical Sciences Tehran Iran.
Mozhgan HashemiehDepartment of Pediatric Hematology and Oncology, School of Medicine, Imam Hossein Medical Center Shahid Beheshti University of Medical Sciences Tehran Iran.
Imam Hossein Hospital · IRImam Khomeini Hospital · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Swyer syndrome is a 46, XY karyotype, with pure gonadal dysgenesis and primary amenorrhea. These females have primordial Mullerian structures and seek medical attention as they experience primary amenorrhea. Here, we report a 15-year-old girl, diagnosed as Swyer syndrome associated with left ovarian dysgerminoma.

Indexed as

dysgerminomapure gonadal dysgenesisSwyer syndrome

Identifiers

PMID35846908
PMCPMC9280751
OpenAlexW4285400678

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.