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white dot syndromes/touse
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Acute posterior multifocal placoid pigment epitheliopathy associated with a systemic necrotizing vasculitis.
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OBJECTIVE
The authors present a case of acute posterior multifocal placoid pigment epitheliopathy (APMPPE) associated with a systemic necrotizing vasculitis with mixed features of Wegener granulomatosis and polyarteritis nodosa (PAN).
METHODS
Case report.
RESULTS
A 29-year-old woman developed a
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