Evidence map›Paper›PMID 29445918›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2018

Persistent craniopharyngeal canal, bilateral microphthalmia with colobomatous cysts, ectopic adenohypophysis with Rathke cleft cyst, and ectopic neurohypophysis: case report and review of the literature.

Nazlı Gülsüm Akyel, Ayşe Gül Alımlı, Tülin Hakan Demirkan, Mesut Sivri

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Disorders Involving a Persistent Craniopharyngeal Canal: A Case Series.Journal of neurological surgery. Part B, Skull base · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. 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

4 authors at 2 institutions in 1 country.

Nazlı Gülsüm AkyelDepartment of Radiology, Ankara Child Health and Diseases Hematology Oncology Training and Research Hospital, University of Health Sciences, Şehit Ömer Halisdemir Cad. Kurtdereli Sok, 06110, Ankara, Altındağ, Turkey. nazligulsumakyel@gmail.com.
Ayşe Gül AlımlıDepartment of Radiology, Ankara Child Health and Diseases Hematology Oncology Training and Research Hospital, University of Health Sciences, Şehit Ömer Halisdemir Cad. Kurtdereli Sok, 06110, Ankara, Altındağ, Turkey.
Tülin Hakan DemirkanDepartment of Radiology, Ankara Child Health and Diseases Hematology Oncology Training and Research Hospital, University of Health Sciences, Şehit Ömer Halisdemir Cad. Kurtdereli Sok, 06110, Ankara, Altındağ, Turkey.
Mesut SivriDepartment of Radiology, Ankara Child Health and Diseases Hematology Oncology Training and Research Hospital, University of Health Sciences, Şehit Ömer Halisdemir Cad. Kurtdereli Sok, 06110, Ankara, Altındağ, Turkey.
Sağlık Bilimleri Üniversitesi · TRMinistry of Health · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPersistent craniopharyngeal canal (PCC) is a rare anomaly of the base of the skull. PCC is defined as a well-corticated osseous canal, extending from the roof of the nasopharynx to the base of the sella over the course of the sphenoid corpus. We reported a PCC case with unique associations. The magnetic resonance imaging findings are discussed. CASE PRESENTATION: We report a case of a 2-year-old boy with persistent craniopharyngeal canal, bilateral microphtalmia with large colobomatous cyst, and ectopic adenohypophysis with Rathke cleft cyst. He also has ectopic neurohypophysis and optic atrophy.

conclusionThe presence of orbital and optic tract malformations, craniofacial and intracranial anomalies, and tumors can accompany craniopharyngeal canals (CCs). MRI is helpful in the evaluation of PCC and associated anomalies in these patients.

Indexed as

Central Nervous System CystsChild, PreschoolChoristomaColobomaHumansMaleMicrophthalmosOsteoarthropathy, Primary HypertrophicPituitary Gland, AnteriorPituitary NeoplasmsColobomatous cystCraniopharyngeal canalCystEctopic neurohypophysisMicrophtalmos with cystRathke cleft

Identifiers

PMID29445918
OpenAlexW2792893426

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.