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
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container_title Annales de biologie clinique (Paris)
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creator Le Guyader, Maïlys
Pineau-Vincent, Fabienne
Lemaire, Pierre
description 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.
doi_str_mv 10.1684/abc.2015.1117
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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects 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
title Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report
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