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Macular serpiginous choroiditis

Description

Serpiginous choroiditis is an inflammation of the choriocapillaris and retinal pigment epithelium (RPE) of unknown etiology, although an autoimmune origin with probable vascular occlusion at the level of the choriocapillaris is suspected. In active lesions, poorly defined creamy borders can be observed in the fundus, possibly showing edema of deep layers of the retina, with the lesions evolving towards chorioretinal atrophy with a typical serpiginous form. In active phases, autofluorescence shows hyperautofluorescent halos surrounding hypoautofluorescent lesions. In chronic lesions, complete hypoautofluorescence with sharp borders is observed. In optical coherence tomography, areas with disruption of the outer layers of the retina and edema coexist with inactive areas of atrophy and fibrosis. It is very important, due to its therapeutic implications, to assess whether there is peripapillary involvement and vitritis. In cases where serpiginous choroiditis is suspected but the peripapillary area is spared, serpiginous-like choroiditis should be suspected. In this clinical case, the IGRA results were negative. Therefore, immunosuppressive treatment was started with a good response.

Comments

Serpiginous choroiditis is a type of posterior uveitis that is difficult to treat, as the lesions frequently reactivate and the involvement of the foveal area can cause drastic loss of visual acuity. Follow-up with autofluorescein and OCT-angiography is important, as well as aggressive immunosuppressive treatment, provided that tuberculous etiology has been ruled out.

Indication

A 53-year-old woman presented with central vision loss, presenting a “dog-shaped” scotoma ( sic ) that had been developing for 2 months. Quantiferon Tb-Gold was negative and the chest X-ray was normal.