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[Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report]
Maïlys Le Guyader1, Fabienne Pineau-Vincent1, Pierre Lemaire1
1Laboratoire d'hématologie et immunologie, Centre Hospitalier, Le Mans, France.
Annales De Biologie Clinique
|January 9, 2016
Abstract:
Paroxysmal nocturnal hemoglobinuria is a rare clonal non-malignant disease, linked to an acquired PIG-A gene mutation. We report the case of 81 years old patient hospitalized for articular ache, swelling and temporal arteries' induration in which we diagnose PNH associated with refractory cytopenia with multilineage dysplasia.

