Affiliation:
1. Klinički centar Niš, Klinika za očne bolesti, Niš
2. Medicinski fakultet, Institut za anatomiju, Niš
Abstract
Introduction. Multifocal choroidopathy syndromes are a group of rare
disorders, which involve a primary pathologic process occurring at or near
the level of the retinal pigment epithelium, with or without choriocapillaris
involvement. The aetiology of multifocal choroidopathy syndrome is still
unknown. A case report. We present a case of multifocal choroidopathy
syndrome. A 54-year-old woman was referred to our department with blurred
vision on both eyes, mild ocular pain, accompanied by metamorphopsia,
floaters, scotomas and photopsia. The anterior segment examination showed
small to medium size keratic precipitates, posterior synechiae, and iris
atrophy. Mild to moderate aqueous inflammation with cells and flair was
present in the anterior chamber. The fundus examination showed multiple small
yellow-white spots, round-shaped changes located at the level of the retinal
pigment epithelium and choriocapillaris. According to the fluorescein
angiography the active lesions exhibited blockage of the early choroidal
fluorescence followed by late staining. The old inactive lesions corresponded
to the retinal pigment epithelium windows defects. The laboratory examination
showed high level of blood glucose, C reactive protein, cholesterol HDL, LDL,
triglycerides. According to the immunological examination the C3 component of
complement was lower (0.630), as well as the C4 component of complement
(0.158), and the immunological complex in blood was elevated (171). ELIZA
test on viral infection showed Citomegalo viruses IgG positive, Herpes
Simplex Virus IgG positive, Varichela Zoster Virus IgG positive. The results
of human leucocyte antigen typization were human leucocyte antigen A1:A2,
human leucocyte antigen A2:A24(9), human leucocyte antigen B1:B44(12), human
leucocyte antigen B2:B60(40), human leucocyte antigen C1:Cw3, human leucocyte
antigen C2:Cw5. The radiological examination of lungs, the Mantoux test,
Treponemal serology, Toxocara and Toxoplasma serology, magnetic resonance of
endocranium and orbit were also performed. The multiple viral infection,
which was detected in our patient with immunological abnormalities pointed to
an underlying autoimmune mechanism, possibly triggered by an infectious
agent, a virus.
Publisher
National Library of Serbia