Evidence map›Paper›PMID 34130443›Full record

ArticlePsychiatry investigation2021

Pseudotumoral Presentation of Cerebral Amyloid-Beta Angiopathy: Case Report and Review of Literature.

Claudia Uribe Roca, Fabio Maximiliano Gonzalez, Marta Ines Bala, Miguel Saucedo, Lucrecia Bandeo, Luciana Leon Cejas, Sol Pacha, Pablo Bonardo, Carlos Rugilo, Pablo Dezanzo and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Psychiatry investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Inflammatory Cerebral Amyloid Angiopathy: A Broad Clinical Spectrum.Journal of clinical neurology (Seoul, Korea) · 2023
    Review
  3. 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

14 authors at 2 institutions in 1 country.

Claudia Uribe RocaDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Fabio Maximiliano GonzalezDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Marta Ines BalaDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Miguel SaucedoDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Lucrecia BandeoDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Luciana Leon CejasDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Sol PachaDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Pablo BonardoDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Carlos RugiloDepartment of Neuroradiology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Pablo DezanzoDepartment of Pathology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Rafael TorinoDepartment of Neurosurgery, Buenos Aires British Hospital, Buenos Aires, Argentina.
Gustavo SevleverDepartment of Pathology, FLENI, Buenos Aires, Argentina.
Manuel Fernandez PardalDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Ricardo ReisinDepartment of Neurology, Buenos Aires British Hospital, Buenos Aires, Argentina.
Hospital Británico de Buenos Aires · ARFundación para la Lucha contra las Enfermedades Neurológicas de la Infancia · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCerebral amyloid angiopathy-related inflammation (CAA-RI) is a rare and potentially treatable encephalopathy that usually affects people older than 50 years old and has an acute or subacute clinical presentation characterized by rapidly evolving cognitive decline, focal deficits and seizures. In a small subset of patients the disease can adopt a pseudotumoral form in the neuroimages that represents a very difficult diagnostic challenge.

methodsHere in we report a patient with a tumour-like presentation of histopathologically confirmed CAA-RI.

resultsWe also conducted a search and reviewed the clinical and radiological features of 41 cases of pseudotumoral CAA-RI previously reported in the literature in order to identify those characteristics that should raise diagnostic suspicions of the disease, there by avoiding unnecessary surgical treatments.

conclusionThe therapy of CAA-RI with steroids is usually effective and clinical and radiological remission can be achieved in the first month in approximately 70% of cases.

Indexed as

Cerebral amyloid angiopathyNeoplasmPseudotumoralTumor-like

Identifiers

PMID34130443
PMCPMC8256143
OpenAlexW3170845857

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.