| Literature DB >> 24172778 |
Joseph Villiers1, Munther Khamashta, Alastair Hepburn.
Abstract
Antiphospholipid syndrome (APS) is characterised by recurrent arterial and/or venous thromboses and recurrent late miscarriages in the presence of antiphospholipid antibodies, and can be a hugely debilitating disorder. While the commonest thrombotic manifestations of this condition such as deep vein thrombosis and stroke are well documented, there has been increasing recognition of numerous less common complications in most organ systems. We present a female patient with APS and a lupus-like illness who had atraumatic sacral fractures as well as multiple spontaneous fractures affecting her ribs and the metatarsals in both her feet.Entities:
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Year: 2013 PMID: 24172778 PMCID: PMC3822211 DOI: 10.1136/bcr-2013-201311
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X