HaNDL with bilateral central venous occlusions

Abstract

BackgroundThe syndrome of Headache and focal Neurological Deficits with cerebrospinal fluid Lymphocytosis (HaNDL) is considered a rare, idiopathic and self-limited condition.MethodsWe present a patient with HaNDL who had unique findings of florid optic disc haemorrhages from bilateral central retinal vein occlusions.ResultsOur patient made a full recovery with conservative management.ConclusionIt is important for medical attendants to recognise that HaNDL syndrome can be associated with neuro-ophthalmic complications.