Evidence map›Paper›PMID 40691633›Full record

ArticleItalian journal of pediatrics2025

Pediatric non-alcoholic Wernicke's encephalopathy: a case report.

Lucia Corso, Laura Lucaccioni, Martina Buttera, Mattia De Agostini, Patrizia Bergonzini, Elisabetta Spezia, Elisa Caramaschi, Diego Biondini, Viviana Durante, Lorenzo Iughetti and 1 more

Abstract readCase Reports
In one paragraph

Article in Italian journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Lucia CorsoPostgraduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy.
Laura LucaccioniPostgraduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy. laura.lucaccioni@unimore.it.ORCID http://orcid.org/0000-0003-0288-8990
Martina ButteraPostgraduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy.
Mattia De AgostiniPostgraduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy.
Patrizia BergonziniPaediatric Unit, Department of Medical and Surgical Sciences of Mothers, Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Elisabetta SpeziaPaediatric Unit, Department of Medical and Surgical Sciences of Mothers, Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Elisa CaramaschiPaediatric Unit, Department of Medical and Surgical Sciences of Mothers, Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Diego BiondiniSurgical Paediatric Unit, Department of Medical and Surgical Sciences of Mothers, Children and Adults, University Hospital of Modena, Modena, Italy.
Viviana DuranteSurgical Paediatric Unit, Department of Medical and Surgical Sciences of Mothers, Children and Adults, University Hospital of Modena, Modena, Italy.
Lorenzo IughettiPostgraduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy.
Barbara PredieriPostgraduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wernicke-Korsakoff syndrome is a neurological disorder caused by thiamine (vitamin B1) deficiency. This encephalopathy is typically suspected in alcoholics adults, but it is important to remember that other less known and suspected causes can determine the development of the non-alcoholic Wernicke's encephalopathy. In non-alcoholic patients, the primary causes of Wernicke's encephalopathy include hyperemesis gravidarum, restrictive diets and malnutrition, cancer, post-operative complications following bariatric surgery. Few data are reported regarding non-alcoholic thiamine deficiency, especially within the paediatric population. We describe the case of an 11-year-old Caucasian male with obesity who experienced prolonged emesis after the beginning of a strictly hypocaloric dietary regimen. This resulted in biliary colic episodes and subsequent necessity for cholecystectomy. The day after surgery, the patient developed acute visual impairment, horizontal nystagmus and diplopia, which were attributed to thiamine deficiency. Wernicke's encephalopathy was suspected, so a blood sample was immediately collected to assay thiamine levels and empiric thiamine supplementation was started. Already from the day after the beginning of the treatment, the patient showed a significant improvement in his clinical conditions. This case study delineates clinical presentation, diagnosis, and treatment of our patient and provides information regarding the red-flag risk factors of non-alcoholic Wernicke's encephalopathy in children. The aim is to increase the likelihood of suspecting the diagnosis and to promptly start the therapy, which is both simple and lifesaving.

Indexed as

Thiamine DeficiencyWernicke EncephalopathyChildHumansMaleThiamineThiamineCase reportGallstoneNystagmusPaediatricThiamine deficiencyWernicke encephalopathy

Identifiers

PMID40691633
PMCPMC12282007

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