Epiteliopatía pigmentaria placoide multifocal aguda asociada a parálisis del VI par craneal
- A. Gibelalde
- A. Bidaguren
- J.I. Ostolaza
- L. Cortázar
- C. Irigoyen
ISSN: 0365-6691
Datum der Publikation: 2009
Ausgabe: 84
Nummer: 3
Seiten: 159-162
Art: Artikel
Andere Publikationen in: Archivos de la Sociedad Española de Oftalmologia
Ziele für nachhaltige Entwicklung
Zusammenfassung
Clinical case: We report the case of a 24-year-old patient who attended our hospital with an acute posterior multifocal placoid pigment epitheliopathy (APMPPE) which was later confirmed by fluorescein angiography. One month after presentation the patient developed a right VI nerve palsy. Discussion: APMPPE is an acute-onset bilateral inflammatory disease causing impaired vision. Although it is thought to be benign, neurologic manifestations have been described even months after presentation. There is no previous report of APMPPE associated with VI nerve palsy.
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