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
Argitalpen urtea: 2009
Alea: 84
Zenbakia: 3
Orrialdeak: 159-162
Mota: Artikulua
Beste argitalpen batzuk: Archivos de la Sociedad Española de Oftalmologia
Garapen Iraunkorreko Helburuak
Laburpena
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.
Erreferentzia bibliografikoak
- Çomu, S, Verstraeten, T, Rinkoff, J, Busis, N. (1996). Neurological manifestations of acute posterior multifocal placoid pigment epitheliopathy. Stroke. 27. 996-1001
- Fishman, GA, Baskin, M, Jednock, N. (1977). Spinal fluid pleocytosis in acute posterior multifocal placoid pigment epitheliopathy. Ann Ophthalmol. 9. 36-46
- Wilson, CA, Choromokos, EA, Sheppard, R. (1988). Acute posterior multifocal placoid pigment epitheliopathy and cerebral vasculitis. Arch Ophthalmol. 106. 796-800
- Schenider, U, Inhoffen, W, Gelisken, F. (2003). Indocyanine green angiography in a case of unilateral recurrent posterior acute multifocal placoid pigment epitheliopathy. Acta Ophthalmol Scand. 81. 72-75
- Lim, LL, Watzke, RC, Lauer, AK, Smith, JR. (2006). Ocular coherence tomography in acute posterior multifocal placoid pigment epitheliopathy. Clin Exp Ophthalmol. 34. 810-812