We present a 46 year old lady with a complicated background history. She was diagnosed with antiphospholipid syndrome after a DVT and PE in 2018 with positive β2-glycoprotein and negative anti-cardiolipin antibodies.
She has a significant neurological history and has attended Neurology outpatient clinics for 10 years. She has a longstanding diagnosis of migraine and has been diagnosed with psychogenic non epileptic seizures after an EMU admission in 2018 as well as functional intermittent left hemiparesis. She has previously had unremarkable MRI imaging of her Brain in 2015
A repeat MRI Brain in January 2019 revealed diffuse left sided meningeal thickening. Serum ACE was elevated at 127 (8-53) but CSF was unremarkable and CSF ACE negative. PET body showed splenomegaly and stable lymphadenopathy. An inguinal lymph node biopsy showed no evidence of malignancy or granulomas.
A repeat MRI Brain in March 2019 showed complete interval resolution of the previously described meningeal thickening.