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Choroidal tuberculomas

Description

Ocular tuberculosis is a form of extrapulmonary involvement of tuberculous infection. It can involve all ocular structures, but most frequently affects the uvea, and the pathophysiology is directly infectious or of autoimmune origin. One of its classic presentations is in the form of choroidal tubercles and tuberculomas, true caseating granulomas that appear as yellow-grayish lesions preferably in the posterior pole and middle periphery. In autofluorescence, lesions with a central hypoautofluorescent nucleus can be observed, which corresponds to the area of necrosis surrounded by a hyperautofluorescent inflammatory halo with poorly defined edges. In optical coherence tomography, the presence of hyporeflective lesions in the choriocapillaris with overlying subretinal fluid in the outer layers of the retina is characteristic.

Comments

Choroidal tuberculomas may lead to exudative retinal detachments and, rarely, to retinal pigment epithelium tears with discharge of purulent material into the vitreous cavity and subsequent endophthalmitis.

Indication

34-year-old male with recently diagnosed HIV infection with CD4 lymphocyte count< 100 cells/mm3 and disseminated tuberculosis infection. Asymptomatic from an ophthalmological point of view