Difficulties of differential diagnosis
of brain alteration in a patient with systemic lupus erythematosus and secondary antiphospholipid
syndrome
Podrazilová L.1, Peterová V.2, Olejárová M.1, Seidl Z.2, Dostál C.1
1Revmatologický ústav, 1. LF UK, Praha 2MR oddělení, Radiodiagnostická klinika, 1. LF UK, Praha |
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Summary:
The authors present a case report of 36-year-old patient suffering from serious neurological symptoms. At
first, manifestation of ischemic cerebral infarction appeared, which was followed by epileptic convulsions.
Finally a diagnosis of systemic lupus erythematosus (SLE) with renal, endocardial, and neuropsychiatric
involvement was established together with secondary antiphospholipid syndrome (APS). It was difficult to
distinguish the etiology of central nervous system (CNS) alterations attested by hyperintense lesions on MRI,
while there were many risk factors of atherogenesis present (male sex, positive family history, corticosteroid
treatment, hypertension, and smoking). SLE vasculitis or antiphospholipid antibody induced vasculopathy
with subsequent microinfarcions is the most likely explanation. However, arterial hypertension or atherosclerotic
induced ischemic lesions within the white matter have to be considered as well.
Key words:
systemic lupus erythematosus, antiphospholipid syndrome, accelerated atherosclerosis,
CNS alteration, magnetic resonance image
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