Antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE) are similar to be characterized by thromboembolic events and various clinical manifestations. We experienced a 21-year-old man with acute iliocaval deep vein thrombosis (DVT). Primary APS was initially diagnosed on the criteria, and after multidisciplinary treatment, iliocaval DVT was gradually regressed. Six months later, the patient complained of acute enteritis, followed by peripheral neuropathy and butterfly lupus. SLE was diagnosed, which suggested that the onset of SLE was preceded by APS. This case raises the question of a present consensus that these two diseases are clearly different clinical entities, although these are closely related.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11669031PMC
http://dx.doi.org/10.3400/avd.cr.24-00040DOI Listing

Publication Analysis

Top Keywords

antiphospholipid syndrome
8
systemic lupus
8
lupus erythematosus
8
iliocaval deep
8
deep vein
8
vein thrombosis
8
preceding antiphospholipid
4
syndrome onset
4
onset systemic
4
erythematosus presenting
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!