Acute posterior multifocal placoid pigment

Acute posterior multifocal placoid pigment epitheliopathy... 

Acute posterior multifocal placoid pigment epitheliopathy is a rare and usually benign and self-limiting chorioretinal disorder, with rapidly deteriorating central vision. However, it can be complicated by systemic vasculitis, aseptic meningitis and stroke (Cornu et al. 1996 de Vries et al. 2006). 

De Vries JJ, den Dunnen WF, Timmerman EA et al. (2006). Acute posterior multifocal placoid pigment epitheliopathy with cerebral vasculitis a multisystem granulomatous disease. Archives of Ophthalmology 124 910-913... 

Three days after recombinant hepatitis B booster immunization, a 31-year-old man developed acute posterior multifocal placoid pigment epitheliopathy (visual loss) and eosinophilia (39,40). 

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