Evidence map›Paper›PMID 34621513›Full record

ArticleF1000Research2021

Case Report: Cerebral venous thrombosis revealing celiac disease.

Romdhane Wiem, Arfa Sondess, Chelly Jihene, Jomaa Olfa, Hammami Sonia, Hmida Karima, El Arbi Fatma, Berriche Olfa

Open access · goldAbstract readCase Reports
In one paragraph

Article in F1000Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 1 institution in 1 country.

Romdhane WiemDepartment of Endocrinology and Internal Medicine, Tahar Sfar University Hospital, Mahdia, 5100, Tunisia.ORCID 0000-0001-8559-0393
Arfa SondessDepartment of Endocrinology and Internal Medicine, Tahar Sfar University Hospital, Mahdia, 5100, Tunisia.ORCID 0000-0001-7797-4899
Chelly JiheneDepartment of Endocrinology and Internal Medicine, Tahar Sfar University Hospital, Mahdia, 5100, Tunisia.
Jomaa OlfaDepartment of Endocrinology and Internal Medicine, Tahar Sfar University Hospital, Mahdia, 5100, Tunisia.
Hammami SoniaFaculty of Medicine, University of Monastir, Monastir, 5000, Tunisia.
Hmida KarimaDepartment of Radiology, Tahar Sfar University Hospital, Mahdia, 5100, Tunisia.ORCID 0000-0001-6960-0301
El Arbi FatmaDepartment of Endocrinology and Internal Medicine, Tahar Sfar University Hospital, Mahdia, 5100, Tunisia.
Berriche OlfaDepartment of Endocrinology and Internal Medicine, Tahar Sfar University Hospital, Mahdia, 5100, Tunisia.
University of Monastir · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Celiac disease (CD) is an autoimmune enteropathy resulting from intolerance of an individual genetically predisposed to gluten. It has a large clinical polymorphism ranging from a classic digestive clinical presentation due to the malabsorption syndrome to extra-intestinal symptoms. Among the hematologic abnormalities, venous thromboembolic disease (VTE) has been reported, and they are most often located in the abdomen or lower limbs, but the cerebral localization was exceptionally described. We report a case of CD revealed by cerebral thrombophlebitis. A 44-year-old patient with no medical history and no drug intake, presented with hemiplegia followed by a status epilepticus in a context of apyrexia, initially hospitalized in intensive care. Magnetic imaging resonance displayed a cerebral venous thrombosis of the sigmoid sinus requiring anticoagulant treatment, then transferred to our department for the etiological investigation. On questioning, the patient reported chronic diarrhea and weight loss with no other associated symptoms. The examination revealed an underweight patient with pale conjunctiva, improvement of her deficit symptoms, and no other abnormalities. Laboratory tests noted biological signs of malabsorption. The thrombophilia assessment revealed a protein C deficiency with a slight increase in anticardiolipin antibodies and anti-Beta 2 glycoprotein 1 antibodies. Immunological tests noted positives anti-transglutaminase and IgA anti-endomysium antibodies. Duodenal biopsy demonstrated villous atrophy. After ruling out the other causes of VTE, the diagnosis of cerebral venous thrombosis secondary to CD was retained. Early diagnosis and treatment of CD improves the quality-of-life for patients and may spare them various long-term or even fatal complications.

Indexed as

Celiac DiseaseVenous ThrombosisAdultAutoantibodiesFemaleGlutensHumansTransglutaminasesAutoantibodiesGlutensTransglutaminasesCeliac disease; venous thromboembolic disease; malabsorption syndrome; Hypercoagulability.

Identifiers

PMID34621513
PMCPMC8447050.2
OpenAlexW3185958305

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Registered trials

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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.