Evidence map›Paper›PMID 35509765›Full record

ArticleCureus2022

Report of a Rare Case of Beta-Thalassemia Major With Subperiosteal Hematomas.

Parag S Mahajan, Jouhar J Kolleri, Sara Ait Souabni, Sakshi Prasad, El Habib Belhaddad, Hussain Mohammed

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2022. 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
0.4field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

6 authors at 3 institutions in 3 countries.

Parag S MahajanClinical Imaging Department, Hamad Medical Corporation, Doha, QAT.
Jouhar J KolleriClinical Imaging Department, Hamad Medical Corporation, Doha, QAT.
Sara Ait SouabniFamily Medicine, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Sakshi PrasadInternal Medicine, National Pirogov Memorial Medical University, Vinnytsya, UKR.
El Habib BelhaddadFamily Medicine, Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, MAR.
Hussain MohammedSurgery Department, Hamad Medical Corporation, Doha, QAT.
National Pirogov Memorial Medical University, Vinnytsya · UACadi Ayyad University · MAHamad Medical Corporation · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beta-thalassemia represents a range of hemoglobinopathies that are a consequence of an impairment in the synthesis of beta-globin chains. They result in different degrees of hemolysis and ineffective erythropoiesis, depending on the underlying mutations. They can lead to severe complications mainly resulting from anemia. However, there is no bleeding tendency in this disorder, and it is uncommon to see hematoma formation in affected patients. To our knowledge, subperiosteal hematomas have been rarely described in the context of beta-thalassemia. Herein, we report a unique case of a 19-year-old boy who was diagnosed with transfusion-dependent beta-thalassemia and secondary hemochromatosis and developed atraumatic subperiosteal hematomas along the humerus.

Indexed as

beta thalassemia majormagnetic resonance imagingmusculoskeletal radiologysubperiosteal hematomaultrasound

Identifiers

PMID35509765
PMCPMC9062281
OpenAlexW4226517298

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.