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VKH

 

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Anterior Uveitis APMPPE ARN ARPE AZOOR Behcet's Birdshot Candida Churg Strauss CMV Drug induced DUSN Endogenous Fungal GCA Herpes zoster Histoplasmosis HSV JIA uveitis Lyme Lymphoma Masquerade MCP MEWDS MS PAN Pars Planitis Phacoanaphylaxis PIC PORN Posterior Uveitis Postoperative Psoriasis PUK Reiter's RP Sarcoidosis Scleritis Serpiginous SFUS SJS SLE SO Syphilis Toxocara Toxoplasmosis Traumatic Tuberculosis Vasculitis VKH White Dot

EYE REPUBLIC Ophthalmology Clinic - Medical Tourism Philippines

 

  1. What is VKH?
  2. What are the extraocular systemic findings of VKH?
  3. What are the ocular findings of VKH?
  4. What are the diagnostic criteria?
  5. What is the clinical course of VKH?
  6. What are the laboratory tests needed?
  7. What is the therapy for VKH?
  8. How do I get more information?

What is VKH?

VKH stands for Vog-Koyanagi-Harada syndrome. It is a systemic disorder involving many organ systems, including the eyes, ears, skin, and meninges.

Nussenblat R, Whitcup S, "Uveitis: Fundamentals and Clinical Practice", Third edition, Mosby-Year Book, 2004.

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What are the extraocular systemic findings of VKH?

There is a prodromal stage, wherein, the patient may complain of headache, orbital pain, stiff neck, and vertigo. Fever, facial weakness, sensorial and behavioral changes may be present. CNS, auditory and skin lesion may be part of the disease complex.

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What are the ocular findings of VKH?

The disease is usually bilateral, although one eye may be inflamed initially. The second eye usually follows within 2 weeks. Vision is decreased with light sensitivity, redness and pain. Your ophthalmologist will see signs of uveitis, scleritis, glaucoma, and other ocular inflammation.

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What are the diagnostic criteria?

COMPLETE VKH (Criteria 1 to 5 must be present)

 

  1. No history of penetrating ocular trauma or surgery preceding the initial onset of uveitis
  2. No clinical or laboratory evidence suggestive of other ocular disease entities
  3. Bilateral ocular involvement (early/late)
  4. Neurological/auditory findings (meningismus, tinnitus, cerebrospinal fluid pleocytosis)
  5. Integumentary finding (alopecia, poliosis, vitiligo)
INCOMPLETE VKH (Criteria 1 to 3 and either 4 or 5 must be present)

 

  1. No history of penetrating ocular trauma or surgery preceding the initial onset of uveitis
  2. No clinical or laboratory evidence suggestive of other ocular disease entities
  3. Bilateral ocular involvement (early/late)
  4. Neurological/auditory findings (meningismus, tinnitus, cerebrospinal fluid pleocytosis)
  5. Integumentary finding (alopecia, poliosis, vitiligo)
PROBABLE VKH (Isolated ocular disease; criteria 1 to 3 must be present)
  1. No history of penetrating ocular trauma or surgery preceding the initial onset of uveitis
  2. No clinical or laboratory evidence suggestive of other ocular disease entities
  3. Bilateral ocular involvement (early/late)

American Journal of Ophthalmology 131:647-652, 2001.

The Vogt-Koyanagi-Harada's (VKH) Disease Committee established the "Revised diagnostic criteria for VKH disease" in 2001.The VKH Committee's revised diagnostic criteria proved useful for VKH disease diagnosis, as the concordance rate for the two criteria was more than 90%. However, patients who had prior cataract surgery or who lacked signs of serous retinal detachment were not classified as having VKH disease because of exclusion by the VKH Committee's new criteria.

Am J Ophthalmol. 2005 Jun;139(6):1080-5. Comparative study of two sets of criteria for the diagnosis of Vogt-Koyanagi-Harada's disease. Kitamura M, Takami K, Kitachi N, Namba K, Kitamei H, Kotake S, Ohno S. Department of Ophthalmology and Visual Sciences, Hokkaido University Graduate School of Medicine, Kita 15 Nishi 7, Kita-ku, Sapporo 060-8638, Japan.

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What is the clinical course of VKH?

The clinical course of VKH is varied with some patients having a limited period of severe ocular inflammatory activity, followed by rapid depigmentation with no further episodes while other patients have continuing chronic disease.

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What are the laboratory tests needed?

  1. Flourescein angiography
  2. Indocyanine green angiography
  3. Electroretinogram and electrooculogram
  4. Lumbar puncture
  5. Glucose tolerance testing
  6. Blood serum testing

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What is the therapy for VKH?

The drug of choice is corticosteroid. Immunosuppresives are given for steroid resistant and chronic recurrent cases.

Corticosteroids at 2 mg/kg/day of prednisone or pulse therapy of 1 g/day methylprednisolone x 3 days followed by 1 mg/kg/day of prednisone

  1. Cyclophosphamide
  2. Chlorambucil 
  3. Azathioprine
  4. Cyclosporinel
  5. FK 506

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How do I get more information?

 

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EYE REPUBLIC Ophthalmology Clinic

Manila

3/F Don Santiago Building Units 309-310

1344 Taft Avenue, Ermita

Manila, 1000 Philippines

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EYE REPUBLIC Ophthalmology Clinic

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Pasig City, 1604, Philippines

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EYE REPUBLIC Ophthalmology Clinic

St. Luke's Medical Center

6/F Cathedral Heights Building Complex (CHBC)

North Tower Suite 614

279 E. Rodriguez Sr. Boulevard

Quezon City, 1102 Philippines

Direct and Fax: (632) 407-3883

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VOGT-KOYANAGI-HARADA SYNDROME information compiled by Dr. Manolette R. Roque and initially uploaded on June 3, 2005.

Last updated on September 14, 2007.

 

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