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Chorea and high antiphospholipid antibodies: probable primary antiphospholipid syndrome
1Department of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.
Insights
Chorea, a movement disorder, can be the first sign of antiphospholipid syndrome. Early screening for antiphospholipid antibodies is recommended for unexplained chorea cases.
Area of Science:
- Neurology
- Rheumatology
- Immunology
Background:
- Antiphospholipid syndrome (APS) is an autoimmune disorder associated with an increased risk of thrombosis and pregnancy morbidity.
- Neurological manifestations of APS are diverse, with chorea being a rare but recognized symptom.
Purpose of the Study:
- To report a case of generalized chorea as the initial presentation of probable primary antiphospholipid syndrome.
- To highlight the importance of considering APS in the differential diagnosis of unexplained chorea.
Main Methods:
- Case report of a young male patient presenting with generalized chorea.
- Comprehensive laboratory investigations including coagulation studies, autoimmune markers, and serological tests.
- Brain magnetic resonance imaging (MRI) to evaluate for neurological abnormalities.
Main Results:
- The patient exhibited involuntary choreiform movements, mild thrombocytopenia, prolonged partial thromboplastin time (PTT), and positive antiphospholipid antibodies (aPL).
- Brain MRI revealed scattered white matter lesions.
- Treatment with aspirin and prednisone led to rapid symptomatic improvement.
Conclusions:
- Chorea can be the inaugural symptom of primary antiphospholipid syndrome.
- Screening for antiphospholipid antibodies should be considered in patients with unexplained chorea.
Abstract:
A young man presented with generalized chorea as the first manifestation of probable primary antiphospholipid syndrome. He was well till 3 months before admission when he started to have involuntary, choreiform movements involving all extremities, the head and the bulbar muscles. Apart from these movements his physical examination was otherwise unremarkable. Laboratory investigations revealed mild thrombocytopenia, high partial thromboplastin time (PTT) only partially corrected by the addition of normal plasma, false positive syphilis serology, weakly positive antinuclear antibody and a high level of IgG anticardiolipin antibodies. Brain magnetic resonance imaging (MRI) showed multiple scattered small areas of high signal intensity on T2 weighted image in the area of centrum semiovale bilaterally. The patient was started on aspirin and prednisone with rapid symptomatic improvement. Despite the difficulty in proving the association between chorea and the high antiphospholipid antibodies, chorea appears in this case to be the initial symptom of primary antiphospholipid syndrome and we suggest screening for antiphospholipid antibodies in unexplained cases of chorea.
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