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Describe ocular tuberculosis and sarcoidosis.

Ophthalmology · 3rd Professional

Ocular Tuberculosis

  • Tuberculosis is among the most important causes of uveitis in INDIA, accounting for a substantial proportion of cases, and it must be considered in every granulomatous, chronic or recurrent uveitis
  • Mechanism — either direct infection by haematogenous spread of Mycobacterium tuberculosis, or a hypersensitivity response to tubercular protein without viable organisms in the eye. The two require different treatment in principle, and cannot reliably be separated in practice — which is the central difficulty of the subject
  • Ocular tuberculosis is frequently isolated: the chest radiograph is often normal and there may be no systemic symptoms at all, so a normal chest film does not exclude it
ManifestationFeatures
Anterior uveitisChronic granulomatous iridocyclitis with mutton-fat KPs, Koeppe and Busacca nodules, broad posterior synechiae and iris granulomas
Choroidal tuberclesSmall, discrete, yellowish-white choroidal lesions, at the posterior pole, seen in miliary tuberculosis — and their presence is a valuable bedside sign of disseminated disease.
Choroidal tuberculomaA large solitary subretinal mass with exudative detachment.
Serpiginous-like choroiditisMultifocal choroiditis spreading in a serpiginoid manner.
Retinal vasculitis — EALES disease
  • An idiopathic obliterative periphlebitis of young adult males, characteristically in INDIA, widely attributed to hypersensitivity to tubercular protein.
  • Presents with recurrent vitreous haemorrhage and floaters; progresses through inflammation, ischaemia and neovascularisation to tractional detachment.
  • Treated with steroid in the inflammatory stage, laser photocoagulation to ischaemic retina, and vitrectomy for non-clearing haemorrhage
OthersScleritis, interstitial keratitis, orbital and lacrimal gland involvement, and optic neuropathy

Ocular Sarcoidosis

  • Sarcoidosis is a multisystem non-caseating granulomatous disease of unknown cause; the eye is involved in 25 to 50%, and uveitis may be the presenting feature
  • Ocular features — granulomatous anterior uveitis with mutton-fat KPs and iris nodules; candle-wax drippings (taches de bougie) — segmental perivenous exudates along the retinal veins, which are characteristic; vitreous snowballs in a "string OF pearls"; multifocal choroiditis; optic disc granuloma; and conjunctival nodules, which are easily biopsied and give a high yield
  • Systemic features — bilateral hilar lymphadenopathy, pulmonary infiltration, erythema nodosum, lupus pernio, arthralgia, hypercalcaemia, and cranial nerve palsy

Applied Aspects

  • Think of tuberculosis in every granulomatous uveitis in India, and do not be reassured by a normal chest radiograph; ocular disease is frequently isolated
  • Examine the fundus in suspected miliary tuberculosis; choroidal tubercles are a quick bedside confirmation of disseminated disease
  • Give steroid alongside antitubercular therapy, not instead of it; the hypersensitivity component worsens paradoxically when the organisms are killed

All questions in Diseases of the Uveal Tract

  1. Q1Describe the anatomy of the uveal tract. Classify uveitis and describe anterior uveitis with its management. ★
  2. Q2Describe intermediate and posterior uveitis with their causes and investigation. ★
  3. Q3Describe the complications of uveitis and the principles of its management. ★
  4. Q4Describe the tumours of the uveal tract. ★
  5. Q5Describe endophthalmitis and panophthalmitis with their management. ★
  6. SN1Describe sympathetic ophthalmitis with its prevention and treatment. ★
  7. SN2Describe keratic precipitates and the other signs of uveitis. ★
  8. SN3Describe ocular tuberculosis and sarcoidosis. ★
  9. SN4Describe ocular toxoplasmosis with its features and management. ★
  10. SN5Describe Vogt-Koyanagi-Harada disease and the other specific uveitic syndromes. ★
  11. SN6Describe uveal coloboma and the congenital anomalies of the iris. ★
  12. SN7Describe HLA-B27 associated uveitis and uveitis in the immunosuppressed.

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