Evidence map›Paper›PMID 39628748›Full record

ArticleCureus2024

A Rare Case of Congenital Factor XIII Deficiency Secondary to Hyperconsumption: A Case Report.

Amukthamalyada Koduri, Jagadeswar Kakumani, Magesh Kumar S

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. 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

3 authors.

Amukthamalyada KoduriGeneral Medicine, Saveetha Medical College, Chennai, IND.
Jagadeswar KakumaniGeneral Medicine, Saveetha Medical College, Chennai, IND.
Magesh Kumar SGeneral Medicine, Saveetha Medical College, Chennai, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acquired Factor XIII (FXIII) deficiency is a rare condition often associated with underlying medical conditions or medications. We present a case of a 23-year-old male, who presented with prolonged bleeding from a traumatic ulcer site on his left leg. Initial laboratory investigations revealed a severe deficiency in FXIII activity (30%) and antigen levels (25%), with no evidence of congenital disorders or other underlying pathologies. Further evaluation indicated a pattern of hyperconsumption due to ongoing bleeding episodes in the form of excessive use of clotting factors due to repeated bleeding episodes and impaired clot stability, leading to a coagulopathy where factors are consumed faster than they can be produced. The patient was treated with six units of cryoprecipitate to address the bleeding and was started on high-end antibiotics, including meropenem and vancomycin, to manage a suspected septic process. This comprehensive approach led to significant clinical improvement, with the resolution of symptoms and stabilization of the ulcer site. This case highlights the importance of considering acquired FXIII deficiency in patients with unexplained bleeding diathesis, especially in the context of alcohol abuse or conditions associated with hyperconsumption. Early recognition and immediate treatment are crucial for improving prognostic outcomes for these patients.

Indexed as

alcohol abusecryoprecipitatefactor xiiihyperconsumptionrare

Identifiers

PMID39628748
PMCPMC11614556

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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.