Panuveitis

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    Panuveitis - Presentation Transcript

    1. Dr. Anupama Karanth
      www.ophthalclass.blogspot.com
      Panuveitis
    2. Classification of uveitis
      Anatomic Classification of Uveitis
      Anterior
      Intermediate
      Posterior
      Panuveitis
      Clinical Classification of Uveitis
    3. Anatomic classification
      Panuveitis
      Primary site of inflammation: anterior chamber, vitreous, retina or choroid
    4. Clinical Classification of Uveitis
      Infectious
      Bacterial / Viral / Fungal / Parasitic / Others
      Non-infectious
      Known/No known systemic association
      Masquerade
      Neoplastic / Non-neoplastic
    5. Panuveitis
    6. Definition
      It is a rare, bilateral, granulomatous panuveitis which occurs after penetrating ocular trauma to one eye, the injured eye is referred to as the exciting eye while the uninjured eye is the sympathizing eye.
      Sensitization to some intraocular antigen/s occurs and results in bilateral ocular inflammation
      Sympathetic ophthalmia
    7. Penetrating injury is the precursor
      Commoner after non-surgical trauma than surgical trauma
      Incarceration of uveal tissue in the wound is a risk factor
      In 80% of cases, presentation is between 2 weeks to 3 months after injury
      May even occur after 50 years
      Sympathetic ophthalmia
    8. Prodromal symptoms in the sympathizing eye (due to iridocyclitis)
      Photophobia
      Blurring to near objects (accommodation affected)
      Redness
      Early signs
      Keratic precipitates
      Retrolental cells and flare
      Sympathetic ophthalmia
    9. Granulomatous iridocyclitis
      Mutton-fat KPs
      Plastic iridocyclitis
      Vitritis
      Multiple yellow white nodules in the choroid – Dalen-Fuchs nodules
      Thickening of uveal tract
      Papillitis
      Can result in blindness in both eyes
      Established disease in both eyes
    10. Prophylaxis
      Enucleation of the injured eye before onset of sympathetic ophthalmia is the only way of prevention, usually within 2 weeks of injury
      ? Enucleation within 2 weeks of onset
      Therapy
      Corticosteroids – topical, periocular, systemic
      Antimetabolites and cyclosporine
      Therapy
    11. A few other common causes of panuveitis….
    12. 10 year history of recurrent bilateral granulomatous uveitis with waxing and waning exudative retinal detachments, on steroids and immunosuppressives…
      www.ophthalclass.blogspot.com
      http://www.aao.org/publications/eyenet/200804/am_rounds.cfm
      • Koeppe and Busacca nodules in the iris
      • Koeppe and Busacca nodules in the iris
      • Extensive pigment alterations in the fundus
      • Koeppe and Busacca nodules in the iris
      • Extensive pigment alterations in the fundus
      • Dalen-Fuchs like peripheral nodules
      • Koeppe and Busacca nodules in the iris
      • Extensive pigment alterations in the fundus
      • Dalen-Fuchs like peripheral nodules
      • Subretinal fibrosis
    13. Bilateral granulomatous iridocyclitis
      Variable vitritis, exudative retinal detachments
      Commoner in pigmented races
      Associated extraocular features important in diagnosis
      CSF pleocytosis, neck stiffness, seizures, paralysis (CNS)
      Vitiligo, alopecia, poliosis (skin)
      Hearing loss and tinnitus (ear)
      Vogt-Koyanagi-Harada disease
    14. Diagnosis
      Classical clinical picture but rule out SO
      CSF lymphocytosis
      Management
      Vigorous use of steroids- local, periocular and systemic
      Immunosuppressives
      Vogt-Koyanagi-Harada disease
    15. A 50 year old diabetic with blurry vision…
      http://www.aao.org/publications/eyenet/200710/am_rounds.cfm
    16. Peripapillary atrophy
    17. Peripapillary atrophy
      Areas of RPE atrophy with underlying large choroidal vessels visible
    18. Peripapillary atrophy
      Areas of RPE atrophy with underlying large choroidal vessels visible
      Pigments in a bony spicule pattern adjacent to vessels
    19. Hereditary
      Retinitis pigmentosa
      Sequelae of auto-immune disease
      Toxic etiologies
      Chloroquine, thioridazine
      Sequelae of infectious disease
      Tuberculosis
      Syphilis
      Lyme disease
      D/D Pigmentary retinopathies
    20. RPR reactive and positive FTA-ABS…… syphilis
    21. Secondary syphilis
      Granulomatous iridocyclitis
      Iris roseola, iris papulosa, iris nodosa
      Focal/multifocal choroiditis
      Retinitis, perivasculitis
      Papillitis, neuroretinitis
      Syphilis – the great masquerader
    22. Management
      Ocular involvement to be treated as neurosyphilis
      CSF evaluation should be done in any syphilitic uveitis
      Penicillin G 2-5 million units IV 4th hourly – 2 weeks
      Steroids only after effective antibiotic therapy
      Syphilis – the great masquerader
    23. A 35 year old male patient with blurry vision…
    24. Hypopyon uveitis, nongranulomatous, vitritis
    25. Core lab tests…Mantoux highly positive, Chest x-ray suggestive….Tuberculosis
    26. Chronic iridocyclitis
      Granulomatous / nongranulomatous
      Choroiditis
      Focal / multifocal / choroidal tubercles
      Retinal vasculitis, vitritis, papillitis
      Difficulty - in establishing the diagnosis and ensuring treatment compliance
      Tuberculosis
    27. A 46 year old lady with floaters…
      http://www.aao.org/publications/eyenet/200801/am_rounds.cfm
    28. Granulomatous KPs, aqueous flare and cells
    29. Infections
      Tuberculosis
      Syphilis
      Lyme disease
      Non-infectious
      Sarcoidosis
      VKH syndrome
      D/D granulomatous iridocyclitis
    30. Chest x-ray, serum ACE…… elevated ACE, hilar lymphadenopathySarcoidosis
    31. Granulomatous KPs
      Bilateral hilar lymphadenopathy
      Conjunctival follicles
      Noncaseatinggranuloma
    32. Multisystem granulomatous disease
      Ocular findings
      Acute / chronic granulomatous iridocyclitis
      Vitreous snowballs
      Retinal periphlebitis, candle wax drippings
      Choroidal small or large granulomas
      Sarcoidosis
    33. Suspect in any uveitis
      Chest x-ray or CT, serum ACE and lysozyme
      Biopsy from skin / conjunctiva / lacrimal gland
      Management
      Corticosteroids – topical, periocular and systemic
      Immunosuppressives may be required
      Sarcoidosis
    34. Behçet’s disease
      Generalized occlusive vasculitis
      Four major criteria
      Oral aphthous ulcers
      Genital ulcers
      Skin – e.g. erythemanodosum
      Ocular inflammation
      Acute iritis with transient hypopyon
      Retinal arteritis, periphlebitis, vitritis
      Ocular disease recurrent and explosive
      Initial immunosuppressives indicated
    35. Aphthous ulcers
      Hypopyoniritis
      Occlusive vasculitis
      Sheathing and optic atrophy

    + Dr. Anupama KaranthDr. Anupama Karanth, 5 months ago

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