Evidence map›Paper›PMID 41328102›Full record

ArticleCureus2025

Recurrent Intramuscular Hematoma Revealing Moderate Congenital Factor XIII Deficiency.

Nada Ben Halima, Salma Riahi, Ines Mazlout, Imen Mgarrech, Amina Bouatay

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 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
–field-weighted citation impact
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

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

5 authors.

Nada Ben HalimaLaboratory of Hematology and Blood Bank/Laboratory of Parasitology, Sahloul Hospital, Faculty of Medicine of Sousse, University of Sousse, Sousse, TUN.
Salma RiahiLaboratory of Hematology and Blood Bank, Sahloul Hospital, Faculty of Medicine of Sousse, University of Sousse, Sousse, TUN.
Ines MazloutDepartment of Cardiovascular and Thoracic Surgery, Sahloul Hospital, Faculty of Medicine of Sousse, University of Sousse, Sousse, TUN.
Imen MgarrechDepartment of Cardiovascular and Thoracic Surgery, Sahloul Hospital, Faculty of Medicine of Sousse, University of Sousse, Sousse, TUN.
Amina BouatayLaboratory of Hematology and Blood Bank, Sahloul Hospital, Faculty of Pharmacy of Monastir, University of Monastir, Sousse, TUN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe congenital factor XIII deficiency is a rare blood coagulation disorder that poses a risk of life-threatening bleeding complications. Conversely, patients with mild or moderate factor XIII deficiency frequently exhibit delayed or provoked bleeding patterns. This case report presents a patient who received a delayed diagnosis of moderate factor XIII deficiency following significant bleeding episodes in the postoperative period. We will examine the symptoms indicative of mild and moderate factor XIII deficiency, as well as the current therapeutic options. This discussion emphasizes the vital importance of early diagnosis for achieving optimal management and improved patient outcomes.

Indexed as

diagnosisfactor xiiihematomahemorrhagetreatment

Identifiers

PMID41328102
PMCPMC12665352

What OpenQuestion holds

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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.