• Med Glas (Zenica) · Feb 2013

    Case Reports

    Acute posterior multifocal placoid pigment epitheliopathy-retinal "white dot syndrome".

    • Desanka Grković, Ana Oros, Tatjana Bedov, Jelena Karadžić, Ljiljana Gvozdenović, and Sandra Jovanović.
    • 1University Eye Clinic, 2Clinic of Anesthesiology and Intensive Care; Clinical Center of Vojvodina, Novi Sad, Srbija.
    • Med Glas (Zenica). 2013 Feb 1; 10 (1): 194196194-6.

    AbstractAcute posterior multifocal placoid pigment epitheliopathy- APMPPE is an acquired idiopathic inflammatory disease of the chorioretina. This case report presents a typical clinical manifestation of a very rare condition: a twenty ive-year old female complained of a sudden bilateral decrease of vision. She reported lu-like symptoms and taking antibiotics therapy. Fundus examination revealed numerous discrete yellow-white lesions at posterior pole involving the macula. After a period of 7 days oral prednisone treatment she was completely recovered. Usage of steroids is recommended for treating APMPPE in cases where macula is involved and in recurrent cases.

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