Challenges in the Diagnosis and Management of Non-Severe Hemophilia

Author:

Boeriu Estera,Arghirescu Teodora Smaranda,Serban Margit,Patrascu Jenel Marian,Boia Eugen,Jinca Cristian,Schramm Wolfgang,Traila Adina,Ursu Cristina EmiliaORCID

Abstract

(1) Background: Mild and moderate hemophilia, synonymous with non-severe hemophilia (NSH), are of constant interest for the clinicians. Bleeding occurs usually after trauma, injury, surgery, or inhibitor development, sometimes leading to a shift of the clinical phenotype from mild to severe, even with life-threatening and unexpected outcomes. (2) Methods: We performed a retrospective observational study conducted on 112 persons with congenital coagulopathies, 26 of them with NSH, admitted to our clinic in the period 2000 to 2022. For the diagnosis, we used laboratory studies (complete blood cell count, coagulation assays, biochemistry, thromboelastography, genetic tests) and imaging investigations (X-ray, ultrasound, CT, MRI). We selected four cases confronted with pitfalls of diagnosis and evolution in order to illustrate the sometimes provocative field of NSH. (3) Results: Confronted with challenging cases with under-, missed or delayed diagnosis and severe consequences, we aimed at presenting four such selected cases with mild or moderate hemophilia, real pitfalls in our clinical activity. (4) Conclusions: In the field of NSH, if not timely recognized, tending sometimes to remain ignored by caregivers and patients themselves, we can be confronted with challenging diagnostic situations and life-threatening bleeds.

Publisher

MDPI AG

Subject

General Medicine

Reference39 articles.

1. WFH Annual Global Survey http://www1.wfh.org/publication/files/pdf-1627.pdf

2. WFH Annual Global Survey https://www1.wfh.org/publications/files/pdf-1731.pdf

3. Hemophilia in Sweden. Studies on demography of hemophilia and surgery in hemophilia and von Willebrand’s disease;Larsson;Acta Med. Scand Suppl.,1984

4. Inhibitor development in haemophilia B: an orphan disease in need of attention

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