Primary antiphospholipid syndrome manifesting as partial status epilepticus.

Abstract

Primary antiphospholipid syndrome (APS) is an autoimmune disease defined by vascular thrombosis, pregnancy complications, and persistent antiphospholipid antibodies. Neurological manifestations include stroke, seizures, and chorea among others. Seizures are often precipitated by an acute ischemic event, but occasionally, structural abnormalities are absent. We present a 61-year-old man who developed partial seizures that progressed into partial status epilepticus. His seizures were intractable and required aggressive treatment with multiple anti-epileptic medications. He was diagnosed with primary APS and treated with anticoagulation. Head imaging did not reveal any acute ischemic events. This case demonstrates that primary APS may present as a refractory status epilepticus unrelated to acute cerebral ischemia.

• Authors: Nancy N Maalouf, Archana Hinduja, Bashir S Shihabuddin
• Journal: Neurosciences (Riyadh, Saudi Arabia) (Neurosciences (Riyadh)) Vol. 18 Issue 2 Pg. 160-2 (Apr 2013) ISSN: 1319-6138 [Print] Saudi Arabia
• PMID: 23545615 (Publication Type: Case Reports, Journal Article)

Chemical References

• Antibodies, Antiphospholipid

Topics

• Antibodies, Antiphospholipid (immunology)
• Antiphospholipid Syndrome (complications, diagnosis, immunology)
• Brain (pathology)
• Electroencephalography
• Humans
• Male
• Middle Aged
• Status Epilepticus (diagnosis, etiology, immunology)