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 Scleritis affects people between the
  ages of 30 and 60 years old, and is very
  uncommon in children.
 Slightly occurs more frequently in
  women.
 Affects a population of more than
  200,000 people, but less than 1 million.
 Scleritis is an inflammation of the sclera, which is the white outer
  wall of the eye.
 It is present within the entirety (depth) of the sclera.
 An eye and/or physical examination with blood tests are used to
  diagnose this disease.
 There are four types:
    › Diffuse anterior: The most common form. Presents with widespread
      inflammation of the anterior sclera. Accounts for 50% of scleritis cases.
    › Nodular: There are erythematous (red), tender, fixed nodules, which, in
      25% of cases progresses to necrotising scleritis. Commonly reccurs.
    › Necrotising: 10% of cases- characterized by extreme pain and marked
      scleral damage. Associated with underlying systemic disease (See:Why?)
    › Scleromalacia perforans: 5% of cases. Known as necrotising without
      inflammation . Notable for lack of symptoms.
   Blurred vision
   Sensitivity to light (can be painful)
   Eye pain and tenderness
   Tearing of the eye
   Fever
   Vomiting
   Headaches
   Red patches on the white part of eyeball
    › Normal cases are mild redness to this area
    › Severe cases are extreme redness to this area
   Normally associated with auto-immune
    diseases such as:
    › Rheumatoid arthritis
    › Systemic lupus erythematosus
    › Sometimes the cause is unknown
 If not treated, significant loss of vision can
  occur.
 Normally treated with oral anti-
  inflammatory medications, corticosteroids,
  and sometimes immunosuppressive drugs,
  depending on the evidence of an
  underlying systemic disease.
 Doesn’t normally respond to topical eye
  drop medications.
 Being based upon certain incurable auto-
  immune diseases, many cases cannot be
  cured, but managed.
   Meisler, D. (1999, June 14). British journal of opthamology.
    Retrieved from http://bjo.bmj.com/content/83/4/410.full
   Carpenter, J. (2002, March 8). John hopkins; depiction of
    scleritis. Retrieved from
    http://www.hopkinsmedicine.org/sebin/b/d/scleritis.jpg
   May, J. (2006, November 21). Legacy: Scleritis . Retrieved
    from http://legacy.revoptom.com/handbook/sect2g.htm
   Mary, D. (2002, January 9). Scleritis; an overview of
    symptoms and treatment. Retrieved from
    http://byebyedoctor.com/scleritis/
   Barry, T. (2001, April 2). Scleritis; about.com. Retrieved from
    http://vision.about.com/od/sportsvision/p/Scleritis.htm

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Scleritis symptoms, types, causes and treatment

  • 1.
  • 2.  Scleritis affects people between the ages of 30 and 60 years old, and is very uncommon in children.  Slightly occurs more frequently in women.  Affects a population of more than 200,000 people, but less than 1 million.
  • 3.  Scleritis is an inflammation of the sclera, which is the white outer wall of the eye.  It is present within the entirety (depth) of the sclera.  An eye and/or physical examination with blood tests are used to diagnose this disease.  There are four types: › Diffuse anterior: The most common form. Presents with widespread inflammation of the anterior sclera. Accounts for 50% of scleritis cases. › Nodular: There are erythematous (red), tender, fixed nodules, which, in 25% of cases progresses to necrotising scleritis. Commonly reccurs. › Necrotising: 10% of cases- characterized by extreme pain and marked scleral damage. Associated with underlying systemic disease (See:Why?) › Scleromalacia perforans: 5% of cases. Known as necrotising without inflammation . Notable for lack of symptoms.
  • 4. Blurred vision  Sensitivity to light (can be painful)  Eye pain and tenderness  Tearing of the eye  Fever  Vomiting  Headaches  Red patches on the white part of eyeball › Normal cases are mild redness to this area › Severe cases are extreme redness to this area
  • 5. Normally associated with auto-immune diseases such as: › Rheumatoid arthritis › Systemic lupus erythematosus › Sometimes the cause is unknown
  • 6.  If not treated, significant loss of vision can occur.  Normally treated with oral anti- inflammatory medications, corticosteroids, and sometimes immunosuppressive drugs, depending on the evidence of an underlying systemic disease.  Doesn’t normally respond to topical eye drop medications.  Being based upon certain incurable auto- immune diseases, many cases cannot be cured, but managed.
  • 7.
  • 8. Meisler, D. (1999, June 14). British journal of opthamology. Retrieved from http://bjo.bmj.com/content/83/4/410.full  Carpenter, J. (2002, March 8). John hopkins; depiction of scleritis. Retrieved from http://www.hopkinsmedicine.org/sebin/b/d/scleritis.jpg  May, J. (2006, November 21). Legacy: Scleritis . Retrieved from http://legacy.revoptom.com/handbook/sect2g.htm  Mary, D. (2002, January 9). Scleritis; an overview of symptoms and treatment. Retrieved from http://byebyedoctor.com/scleritis/  Barry, T. (2001, April 2). Scleritis; about.com. Retrieved from http://vision.about.com/od/sportsvision/p/Scleritis.htm