@article{10.11648/j.ijovs.20210601.15,
  author = {Deepesh Arora and Kanika Gupta and Ankit Parasher and Deepak Anthwal and Niyaaz Ahmad and Dinesh Sharma},
  title = {Vogt-Koyanagi-Harada Disease and Vogt-Koyanagi-Harada Resembling Syndrome},
  journal = {International Journal of Ophthalmology & Visual Science},
  volume = {6},
  number = {1},
  pages = {29-40},
  doi = {10.11648/j.ijovs.20210601.15},
  url = {https://doi.org/10.11648/j.ijovs.20210601.15},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijovs.20210601.15},
  abstract = {Background: To present myriad and unique presentation of Vogt-Kayanagi-Harada Disease (VKHD) and Vogt-Koyanagi-Harada (VKH) resembling syndrome. Methods: This is observational series of four cases of VKH disease with variable unique visual presentation which ranged from blurring of vision, tinnitus, hot flushes on face and abdomen, presence of floaters with hedache, breathlessness and history of weight loss. The patient age ranged from 14-56 years. Symptoms developed acutely ranging from 4-12 weeks. Visual acuity varied from 1/60 to 6/6 on Snellen chart. A detailed ophthalmic evaluation, radio imaging and neuroimaging were done as needed on patients. FFA confirmed disc leakage, subretinal pooling of dye in posterior pole and pin point leaks in three cases. The fourth case revealed dilated capillaries, pin point leaks outside zone of hyperflourescence and presence of leopard spots.USG B-scan in same case showed choroidal thickening and an oval hypointense juxtapappilary lesion. OCT-macula revealed a convex retinal profile, thickening of retinal pigment epithelium choriocapillaries complex, multiple subretinal low reflective areas consisting with serous neurosensory detachment and hyper reflective spots in inner retinal areas consistent with findings suggestive of metastasis. All four patients presented in acute uveitic stage. Barring one patient, three patients had bilateral disease. Incomplete VKH disease was diagnosed in three cases. Metastatic intraocular carcinoma with multiorgan involvement with primary in cervix was diagnosed in one case. Two cases of VKH disease were in remission having responded well to oral steroids and immunesuppresive therapy. One case passed to chronic stage with visual deterioration. One case with multi-organ metastasis went on to receive chemotherapy, brachytherapy, whole body and pelvic radiation. Conclusions: VKH disease has variable presentation and a high degree of suspicion is needed to differentiate it from similar occurring malignant and non-malignant intraocular inflammation. Early staging of VKH disease helps in planning adequate treatment leading to greater improvement in disease outcome and simultaneously preventing progression to chronic stage.},
 year = {2021}
}

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TY  - JOUR
T1  - Vogt-Koyanagi-Harada Disease and Vogt-Koyanagi-Harada Resembling Syndrome
AU  - Deepesh Arora
AU  - Kanika Gupta
AU  - Ankit Parasher
AU  - Deepak Anthwal
AU  - Niyaaz Ahmad
AU  - Dinesh Sharma
Y1  - 2021/02/26
PY  - 2021
N1  - https://doi.org/10.11648/j.ijovs.20210601.15
DO  - 10.11648/j.ijovs.20210601.15
T2  - International Journal of Ophthalmology & Visual Science
JF  - International Journal of Ophthalmology & Visual Science
JO  - International Journal of Ophthalmology & Visual Science
SP  - 29
EP  - 40
PB  - Science Publishing Group
SN  - 2637-3858
UR  - https://doi.org/10.11648/j.ijovs.20210601.15
AB  - Background: To present myriad and unique presentation of Vogt-Kayanagi-Harada Disease (VKHD) and Vogt-Koyanagi-Harada (VKH) resembling syndrome. Methods: This is observational series of four cases of VKH disease with variable unique visual presentation which ranged from blurring of vision, tinnitus, hot flushes on face and abdomen, presence of floaters with hedache, breathlessness and history of weight loss. The patient age ranged from 14-56 years. Symptoms developed acutely ranging from 4-12 weeks. Visual acuity varied from 1/60 to 6/6 on Snellen chart. A detailed ophthalmic evaluation, radio imaging and neuroimaging were done as needed on patients. FFA confirmed disc leakage, subretinal pooling of dye in posterior pole and pin point leaks in three cases. The fourth case revealed dilated capillaries, pin point leaks outside zone of hyperflourescence and presence of leopard spots.USG B-scan in same case showed choroidal thickening and an oval hypointense juxtapappilary lesion. OCT-macula revealed a convex retinal profile, thickening of retinal pigment epithelium choriocapillaries complex, multiple subretinal low reflective areas consisting with serous neurosensory detachment and hyper reflective spots in inner retinal areas consistent with findings suggestive of metastasis. All four patients presented in acute uveitic stage. Barring one patient, three patients had bilateral disease. Incomplete VKH disease was diagnosed in three cases. Metastatic intraocular carcinoma with multiorgan involvement with primary in cervix was diagnosed in one case. Two cases of VKH disease were in remission having responded well to oral steroids and immunesuppresive therapy. One case passed to chronic stage with visual deterioration. One case with multi-organ metastasis went on to receive chemotherapy, brachytherapy, whole body and pelvic radiation. Conclusions: VKH disease has variable presentation and a high degree of suspicion is needed to differentiate it from similar occurring malignant and non-malignant intraocular inflammation. Early staging of VKH disease helps in planning adequate treatment leading to greater improvement in disease outcome and simultaneously preventing progression to chronic stage.
VL  - 6
IS  - 1
ER  - 

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