Paroxysmal nocturnal haemoglobinuria: a case presenting with isolated thrombocytopenia

Paroxysmal nocturnal haemoglobinuria (PNH) is a rare disease characterized by intravascular haemolysis, haemoglobinuria and thrombosis. The present study reported PNH patients presenting with isolated thrombocytopenia. A 31-year-old male patient was referred to haematology outpatient clinic because...

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Bibliographic Details
Main Authors: Mustafa Yilmaz, Beyhan Guvercin, Ceren Konca
Format: Article
Language:English
Published: Taylor & Francis Group 2016-03-01
Series:Biotechnology & Biotechnological Equipment
Subjects:
Online Access:http://dx.doi.org/10.1080/13102818.2015.1112750
Description
Summary:Paroxysmal nocturnal haemoglobinuria (PNH) is a rare disease characterized by intravascular haemolysis, haemoglobinuria and thrombosis. The present study reported PNH patients presenting with isolated thrombocytopenia. A 31-year-old male patient was referred to haematology outpatient clinic because of thrombocytopenia detection. Initially, there was no anaemia, but apparent haemolytic anaemia occurred in the patient within a year. The PNH was diagnosed by using fluorescently labelled inactive variant of the protein aerolysin test. Anaemia, jaundice, thrombosis, fatigue, dyspnoea, dark urine, abdominal or gastric pain, dysphagia and erectile dysfunction are primary symptoms of PNH, leading to diagnosis. This is an atypical PNH case presenting with isolated thrombocytopenia, which led to difficulty and delay in diagnosis.
ISSN:1310-2818
1314-3530