Evidence map›Paper›PMID 31662812›Full record

ReviewPain research & management2019

Recurrent Painful Ophthalmoplegic Neuropathy and Oculomotor Nerve Schwannoma: A Pediatric Case Report with Long-Term MRI Follow-Up and Literature Review.

Maria Giuseppina Petruzzelli, Mariella Margari, Flora Furente, Maria Carmela Costanza, Anna Rosi Legrottaglie, Franca Dicuonzo, Lucia Margari

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in Pain research & management, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Neuroimaging of a Paediatric Ophthalmoplegic Migraine.Annals of Indian Academy of Neurology
    Article
  8. 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

7 authors at 1 institution in 1 country.

Maria Giuseppina PetruzzelliDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari "Aldo Moro", Bari, Italy.ORCID 0000-0003-1734-788X
Mariella MargariDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari "Aldo Moro", Bari, Italy.
Flora FurenteDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari "Aldo Moro", Bari, Italy.
Maria Carmela CostanzaDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari "Aldo Moro", Bari, Italy.
Anna Rosi LegrottaglieDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari "Aldo Moro", Bari, Italy.
Franca DicuonzoDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari "Aldo Moro", Bari, Italy.
Lucia MargariDepartment of Basic Medical Sciences, Neurosciences and Sense Organs Department, University of Bari "Aldo Moro", Bari, Italy.ORCID 0000-0002-9203-3373
University of Bari Aldo Moro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recurrent painful ophthalmoplegic neuropathy (RPON), previously known as ophthalmoplegic migraine (OM), is an uncommon disorder with repeated episodes of ocular cranial nerve neuropathy associated with ipsilateral headache. The age of presentation is most often during childhood or adolescence. MRI has a central role in the assessment of the RPON, especially to distinguish orbital, parasellar, or posterior fossa lesions that mimic symptoms of RPON. Actually, oculomotor nerve tumors may be masquerade as RPON so that MRI follow-ups are required to detect the possibility of tumor etiology. Case presentation: We report a 16-year-old boy with a 7-year follow-up and multiple brain MRI data, previously diagnosed as OM. The last brain MRI, performed during an acute phase of oculomotor paresis with ipsilateral headache, showed a nodular lesion described as schwannoma of III cranial nerve. Then, we reviewed the literature on OM and RPON in pediatric age with a focus on brain MRI findings. Conclusions: This review highlights the important role of serial brain MRIs in the long-term follow-up of RPON, especially in the cases with childhood onset, in order to not delay the diagnosis of a possible oculomotor nerve schwannoma.

Indexed as

AdolescentCranial Nerve NeoplasmsFollow-Up StudiesHumansMagnetic Resonance ImagingMaleNeurilemmomaOculomotor Nerve DiseasesOphthalmoplegic Migraine

Identifiers

PMID31662812
PMCPMC6778936
OpenAlexW2975583547

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.