| Literature DB >> 28447244 |
Marc Sorigue1, Jordi Juncà2, Elisa Orna2, Nevena Romanic3, Edurne Sarrate4, Jordi Castellvi3, Montse Soler3, Ines Rodríguez-Hernandez2, Evarist Feliu2, Susana Ruiz3.
Abstract
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disorder associated with increased risk for thrombosis and reduced life expectancy. Retinal vein occlusion (RVO) is a frequent cause of vision loss but its relationship with PNH has not been studied systematically. Patients followed up for RVO in our ophthalmology department were screened for the presence of a PNH clone in peripheral blood by means of flow cytometry. The presence of other well-documented risk factors for RVO was also analyzed. In a series of 110 patients (54 males, median age of 67) we found no evidence of PNH. Most patients (97/110) had cardiovascular risk factors and/or hyperhomocysteinemia (67/110). Inherited thrombophilias were rare (three confirmed cases). Therefore, PNH does not appear to play a role in the development of RVO. However, this finding does not necessarily apply to young patients and/or those with no conventional risk factors for RVO, due to the low number of patients in these subgroups in our population.Entities:
Keywords: Flow cytometry; Paroxysmal nocturnal hemoglobinuria; Retinal vein occlusion; Thrombophilia
Mesh:
Year: 2017 PMID: 28447244 DOI: 10.1007/s11239-017-1502-4
Source DB: PubMed Journal: J Thromb Thrombolysis ISSN: 0929-5305 Impact factor: 2.300