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CASE PRESENTATION  Dr. PRABHA
22yr old male presented with sudden loss of vision left eye of 12 days duration associated with photophobia , watering  and  metamorphopsia Past history of penetrating injury with uveal tissue prolapse RE eye 2 months back for which emergency wound repair done & treated with systemic & topical steroids & antibiotics
GENERAL EXAMINTION  Moderately built & nourished  No pallor , cyanosis , jaundice , clubbing , lymphadenopathy  No vitiligo , alopecia PR – 82/mt BP – 140 / 60 mmHg
SYSTEMIC  EXAMINATION  CNS – no convulsions , no FND  CVS – Loud S2 GIT – no organomegaly  RESP – NAD  MSK – NAD
OCULAR EXAMINATION  Vision  - RE CF ½ m                  LE  6/36
                    RIGHT EYE  Lid & adnexa no poliosis , vitiligo  Conjuctival congestion  Sutured full thickness corneoscleral wound from limbus at 9 o’clock to 6o’clock and is extended 2mm to the sclera  AC cells 2+  Flare 2+ Pupil dilated pharmacologically   Iris deficient at 6 o’clock
                          RIGHT EYE Lens phacodonesis+ Rosette cataract AVF– no cells  FUNDUS – media hazy due to cataractous lens & coarse vitreous floaters  Disc & vessels normal  FR dull Organized vitreous hge inferiorly
                LEFT EYE Conjuctival congestion Cornea clear AC cells 1+ Flare 1+ Pupil dilated pharmacologically   Lens clear AVF– no cells
                      LEFT EYE FUNDUS – media clear  Disc & vessels normal  CDR – 0.3 , NRR pink & even  Macular edema with ILM folds + 3 to 4 small yellowish white subretinal lesion seen just superior to macula Serous detachment of retina of 3DD seen between IT & IN  arcade starting from the inferior disc margin
INVESTIGATIONS Hb – 14.8 gm% TC – 12600 ccmm DC – N81 , L 18 . E2  ESR- 3mm/hr RBS – 110  BUN – 39mg% S creatinine – 0.7% S.biliribin – 1mg5  ALP – 202 IU SGOT – 42 IU SGPT-24IU Platelet – 3L PS- mild neutrophilia
FFA – hyperfluorescent , pin point leaks in peripapillary area which persists in late phase  Hypofluorescent area with late staining seen superior to macula
B scan  RE – vitreous floaters  LE – serous RD WITH CHOROIDAL THICKENING
                        LEFT EYE
                  RIGHT EYE
DIAGNOSIS OLD OPEN GLOBE INJURY TYPE B GRADE D PUPIL B ZONE 2 WITH VITREOUS HEMORRHAGE WITH ANTERIOR UVEITIS RE POSTERIOR UVEITIS WITH SPILL OVER ANTERIOR UVEITIS LE     – SYMPATHETIC OPHTHALMIA
TREATMENT Gatiquin P eye Drops QID BE  Homide eye drops BD BE Inj Methyl prtednisolone 500mg IV BD – 7D followed by  Inj Dexamethasone 2cc IM OD T. Azoran 50mg  BD
On discharge  Vision CF 1m RE ,NIG NIP               6/12 LE ,NIG NIP BE – AC no cells & flare  LE – serous detchment & macular edema reduced
SYMPATHETIC OPHTHALMIA It is a rare bilateral diffuse granulamatous non necrotizing panuveitis that may develop after either surgical or accidental trauma to one eye ( exciting eye ) followed by latent period and the appearance of uveitis in uninjured fellow eye                      ( sympathizing eye)
Incidence recently estimated is 0.03 per 1 lakh population  Key features are  Bilateral anterior or posterior uveitis of variable severity with uniform choroiditis Associated features Dalen-Fuch spots, papillitis , dysacousis , tinnitus , alopecia , poliosis , vitiligo , headache.
    Histopathology Shows predominantly consists of mononuclear and epitheloid cells  Choriocapillaries are spared   Immunohistopathology  ,[object Object],[object Object]
          TREATMENT  Enucleation of the inciting eye as a treatment modality is still controversy  Treatment should address the T cell mediated nature of the disease  Large doses of topical & systemic corticosteroids should be given early in he course of the disease  Other immunosuppressive therapies may be considered isolated or in association with steroids
PROGNOSIS visual prognosis is good with 50% of patient achieving a final visual acuity of 20/40 or better in at least one eye  The cause of sympathetic ophthalmia is chronic with frequent exacerbations and if left untreated leads to loss of vision & phthisis bulbi Long term follow up is essential
Syp op dr prabha

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Syp op dr prabha

  • 1. CASE PRESENTATION Dr. PRABHA
  • 2. 22yr old male presented with sudden loss of vision left eye of 12 days duration associated with photophobia , watering and metamorphopsia Past history of penetrating injury with uveal tissue prolapse RE eye 2 months back for which emergency wound repair done & treated with systemic & topical steroids & antibiotics
  • 3. GENERAL EXAMINTION Moderately built & nourished No pallor , cyanosis , jaundice , clubbing , lymphadenopathy No vitiligo , alopecia PR – 82/mt BP – 140 / 60 mmHg
  • 4. SYSTEMIC EXAMINATION CNS – no convulsions , no FND CVS – Loud S2 GIT – no organomegaly RESP – NAD MSK – NAD
  • 5. OCULAR EXAMINATION Vision - RE CF ½ m LE 6/36
  • 6. RIGHT EYE Lid & adnexa no poliosis , vitiligo Conjuctival congestion Sutured full thickness corneoscleral wound from limbus at 9 o’clock to 6o’clock and is extended 2mm to the sclera AC cells 2+ Flare 2+ Pupil dilated pharmacologically Iris deficient at 6 o’clock
  • 7. RIGHT EYE Lens phacodonesis+ Rosette cataract AVF– no cells FUNDUS – media hazy due to cataractous lens & coarse vitreous floaters Disc & vessels normal FR dull Organized vitreous hge inferiorly
  • 8. LEFT EYE Conjuctival congestion Cornea clear AC cells 1+ Flare 1+ Pupil dilated pharmacologically Lens clear AVF– no cells
  • 9. LEFT EYE FUNDUS – media clear Disc & vessels normal CDR – 0.3 , NRR pink & even Macular edema with ILM folds + 3 to 4 small yellowish white subretinal lesion seen just superior to macula Serous detachment of retina of 3DD seen between IT & IN arcade starting from the inferior disc margin
  • 10.
  • 11. INVESTIGATIONS Hb – 14.8 gm% TC – 12600 ccmm DC – N81 , L 18 . E2 ESR- 3mm/hr RBS – 110 BUN – 39mg% S creatinine – 0.7% S.biliribin – 1mg5 ALP – 202 IU SGOT – 42 IU SGPT-24IU Platelet – 3L PS- mild neutrophilia
  • 12. FFA – hyperfluorescent , pin point leaks in peripapillary area which persists in late phase Hypofluorescent area with late staining seen superior to macula
  • 13.
  • 14. B scan RE – vitreous floaters LE – serous RD WITH CHOROIDAL THICKENING
  • 15. LEFT EYE
  • 16. RIGHT EYE
  • 17. DIAGNOSIS OLD OPEN GLOBE INJURY TYPE B GRADE D PUPIL B ZONE 2 WITH VITREOUS HEMORRHAGE WITH ANTERIOR UVEITIS RE POSTERIOR UVEITIS WITH SPILL OVER ANTERIOR UVEITIS LE – SYMPATHETIC OPHTHALMIA
  • 18. TREATMENT Gatiquin P eye Drops QID BE Homide eye drops BD BE Inj Methyl prtednisolone 500mg IV BD – 7D followed by Inj Dexamethasone 2cc IM OD T. Azoran 50mg BD
  • 19. On discharge Vision CF 1m RE ,NIG NIP 6/12 LE ,NIG NIP BE – AC no cells & flare LE – serous detchment & macular edema reduced
  • 20. SYMPATHETIC OPHTHALMIA It is a rare bilateral diffuse granulamatous non necrotizing panuveitis that may develop after either surgical or accidental trauma to one eye ( exciting eye ) followed by latent period and the appearance of uveitis in uninjured fellow eye ( sympathizing eye)
  • 21. Incidence recently estimated is 0.03 per 1 lakh population Key features are Bilateral anterior or posterior uveitis of variable severity with uniform choroiditis Associated features Dalen-Fuch spots, papillitis , dysacousis , tinnitus , alopecia , poliosis , vitiligo , headache.
  • 22.
  • 23. TREATMENT Enucleation of the inciting eye as a treatment modality is still controversy Treatment should address the T cell mediated nature of the disease Large doses of topical & systemic corticosteroids should be given early in he course of the disease Other immunosuppressive therapies may be considered isolated or in association with steroids
  • 24. PROGNOSIS visual prognosis is good with 50% of patient achieving a final visual acuity of 20/40 or better in at least one eye The cause of sympathetic ophthalmia is chronic with frequent exacerbations and if left untreated leads to loss of vision & phthisis bulbi Long term follow up is essential