Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report

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 cytop...

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Veröffentlicht in:	Annales de biologie clinique (Paris) 2016-01, Vol.74 (1), p.106-109
Hauptverfasser:	Le Guyader, Maïlys, Pineau-Vincent, Fabienne, Lemaire, Pierre
Format:	Artikel
Sprache:	fre
Schlagworte:	Aged, 80 and over Diabetes Mellitus, Type 2 - complications Hemoglobinuria, Paroxysmal - complications Hemoglobinuria, Paroxysmal - pathology Humans Male Myelodysplastic Syndromes - complications Myelodysplastic Syndromes - pathology Urolithiasis - complications
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Zusammenfassung:	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.
ISSN:	1950-6112
DOI:	10.1684/abc.2015.1117