| Literature DB >> 26847804 |
Luísa Azevedo1, Mariana Reis Costa1, Ana Catarina Fonseca1, Teresa Pinho e Melo1.
Abstract
The authors present a case of a 28-year-old man with a known history of paroxysmal nocturnal haemoglobinuria (PNH), under platelet antiaggregation, admitted following recurrent transitory arterial ischaemic attacks. Concomitant thrombosis of the superior mesenteric artery and bilateral renal infarction was found. Cardioembolism, namely patent foramen ovale, was excluded and anticoagulation added, with no further events on 10-month follow-up. PNH is a rare acquired disorder of haematopoietic stem cells, characterised by haemolytic anaemia, pancytopenia and thrombotic events classically involving the venous system. Reports of cerebral artery stroke and accompanying intra-abdominal arterial thrombosis are especially rare. Complementary investigation and treatment options in these patients are discussed. 2016 BMJ Publishing Group Ltd.Entities:
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Year: 2016 PMID: 26847804 PMCID: PMC4746544 DOI: 10.1136/bcr-2015-213603
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X