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Retinal vasculitis associated with tuberculosis

Description

Retinal vasculitis associated with tuberculosis is a heterogeneous and difficult to manage entity. It is characterized by occlusive retinal vasculitis, predominantly venous, with associated vitritis and peripheral retinal ischemia in patients with evidence of tuberculosis by laboratory test or biopsy. It typically appears as peripheral periphlebitis with a tendency to capillary closure and neovascularization. The lack of consensus in the diagnosis and management of this entity can lead to sequelae. Treatment is based on the use of antituberculosis drugs accompanied or not by oral steroid treatment and even immunosuppressants. Treatment success is defined as the resolution of inflammatory signs 6 months after finishing treatment, the ability to reduce the dose of oral steroids below 10 mg/day or 1 drop of oral steroids maximum every 12 hours. Sometimes, local complications such as neovascularization or tractional retinal detachment require additional treatment.

Comments

Did you know that this case shows a possible paradoxical paucibacillary reaction enhanced by the release of antigens after the start of antituberculosis treatment?

Indication

A 24-year-old woman from Iran came to the emergency room with a 24-hour history of floaters in her right eye. The patient had recently started antituberculosis treatment with isoniazid and rifampicin after a recent positive Mantoux test. On examination, she had a cellular reaction of +++/++++ in the anterior chamber and fundus, papilledema, vascular ensheathment and haemorrhages. Fluorescein angiography showed diffuse periphlebitis with peripheral occlusions. The chest tube showed lesions compatible with pulmonary tuberculosis, and the sputum was positive for Mycobacterium tuberculosis . The patient was receiving treatment for tuberculosis with four drugs and high-dose steroids. On discharge, visual acuity was 1 in AO and she had no inflammatory signs.