Evidence map›Paper›PMID 36982983›Full record

ArticleInternational journal of molecular sciences2023

An Uncommon Case of Moyamoya Syndrome Is Accompanied by an Arteriovenous Malformation with the Involvement of Dural Arteries.

Chingiz Nurimanov, Iroda Mammadinova, Yerbol Makhambetov, Serik Akshulakov

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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 1 institution in 1 country.

Chingiz NurimanovVascular and Functional Neurosurgery Department, National Center for Neurosurgery, Astana 010000, Kazakhstan.
Iroda MammadinovaVascular and Functional Neurosurgery Department, National Center for Neurosurgery, Astana 010000, Kazakhstan.ORCID 0000-0002-0427-1751
Yerbol MakhambetovVascular and Functional Neurosurgery Department, National Center for Neurosurgery, Astana 010000, Kazakhstan.
Serik AkshulakovVascular and Functional Neurosurgery Department, National Center for Neurosurgery, Astana 010000, Kazakhstan.
National Research Center for Maternal and Child Health · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: This report describes the surgical management of a case of concurrent AVM with the involvement of dural arteries and moyamoya syndrome. Given the infrequency of this combination, there is currently no established management strategy available. (2) Case Description: A 49-year-old male patient with multiple symptoms including headaches, tinnitus, and visual impairment diagnosed with the coexistence of an arteriovenous malformation with the involvement of dural arteries and moyamoya syndrome was admitted to the national tertiary hospital. The patient underwent surgical management through embolization of the AVM from the afferents of the dural arteries, which has resulted in positive clinical outcomes. However, this approach may not be suitable for all cases, and a multidisciplinary team approach may be required to develop an individualized treatment strategy. (3) Conclusion: The contradictory nature of the treatment approaches in cases of combined AVM with the involvement of dural arteries and MMD highlights the complex nature of this condition and the need for further research to identify the most effective treatment strategies.

Indexed as

Intracranial Arteriovenous MalformationsMoyamoya DiseaseArteriesHumansMaleMiddle AgedTreatment Outcomearteriovenous fistulaarteriovenous malformationmoyamoya syndromesurgical management

Identifiers

PMID36982983
PMCPMC10056675
OpenAlexW4328110120

What OpenQuestion holds

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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.