| Literature DB >> 31219421 |
Jérôme Debus1, Bénédicte Dumont1, Camille Le Breton2, Malo Emery2, Edith Peynaud-Debayle1, Louis Affo3.
Abstract
We report here a case of bone marrow necrosis and fat embolism syndrome in a 23-year-old sickle-cell disease (HbSS) patient. A brutal and severe bicytopenia conducted to suspect bone marrow necrosis, confirmed by bone marrow aspiration and analysis. This was the first life-threatening medical event for this patient. In the present case, a complex alloimmunization against blood group antigens complicated the treatment because of the risks associated with the transfusion strategy. These rare complications of sickle-cell disease may be fatal, but an efficient symptomatic treatment generally allows for recovery. Medical biologists should be aware of the danger of bone marrow necrosis in sickle-cell disease, so that they can help clinicians and accurately diagnose this serious complication.Entities:
Keywords: alloimmunization; bone marrow necrosis; fat embolism; sickle-cell disease; vaso-occlusive crisis
Mesh:
Year: 2019 PMID: 31219421 DOI: 10.1684/abc.2019.1451
Source DB: PubMed Journal: Ann Biol Clin (Paris) ISSN: 0003-3898 Impact factor: 0.459