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Giant cell arteritis
AGUN M.I
Case Presentation
• A 64
VASCULITIS
VASCULITIS(Pauci immune complexes)
Primary or Secondary
Systemic or Cutaneous
Large vessel- Giant Cell arteritis, Takayasu
Medium vessel-Polyarteritis nodosa, Behcet’s Disease, Kawasaki
Small vessel(AASV)- Wegeners Granulomatosis, Churg-Strauss,
Microscopic Polyangiitis.
Secondary vasculitis- RA,SLE,HIV,HCV,HBV Syphilis,Drugs-
(sulphonamides,ofloxacin),infections meningococcus,Staph,
Introduction
• Giant cell arteritis (GCA) is a disease of blood vessels, may occur
together with polymyalgia rheumatica.
• GCA occurs only in older adults, mainly those over age of 50, and
can cause swelling and thickening of the small artery under the
skin called the temporal artery.
• A new, persisting headache is a common symptom of GCA.
Symptoms of GCA promptly improve with corticosteroids.
• If GCA affects blood flow to the eye, loss of vision can occur.
Prompt detection and treatment of GCA can prevent loss of vision.
• GCA is a type of vasculitis or arteritis, a group of diseases whose
main feature is inflammation of blood vessels.
• In GCA, the vessels most often involved are the arteries of the
scalp and head, especially the arteries over the temples, which is
why another term for GCA is “temporal arteritis.”
Symptoms
• Persistent, severe head pain, usually in your temple area
• Scalp tenderness
• Jaw pain when you chew or open your mouth wide
• Fever
• Fatigue
• Unintended weight loss
• Vision loss or double vision, particularly in people who also have jaw
pain
• Sudden, permanent loss of vision in one eye( however proper treatment
can prevent this complication.)
Diagnosis
• There is no simple blood test or non invasive way to confirm the
diagnosis of GCA.
• The erythrocyte sedimentation rate (or sed rate) is a blood test
that measures inflammation by checking to see how the rate at
which red blood cells (erythrocytes) sediment (or fall) within an
hour.
• This rate is high in most people with GCA.
Diagnosis
• It is common to do a biopsy – or surgical removal – of a small piece
of the temporal artery and study it under a microscope for signs of
inflammation.
• This biopsy is an outpatient procedure, done under local
anesthesia (numbing of that site while you are awake). It leaves
just a small scar that usually cannot be seen at the hairline in
front of the ear.
• In GCA, the biopsy shows inflammation of the artery
Management
• The treatment for GCA should begin as soon as possible because of
the risk of loss of vision.
• If you doctor strongly suspects GCA, treatment can start before
you get the results of a temporal artery biopsy.
• GCA treatment usually involves high doses of corticosteroids.
Typically, the dose is 40-60 milligrams (mg) per day of prednisone .
Headaches and other symptoms quickly decrease with treatment,
and the sedimentation rate declines to a normal range.
Mgt Contd
• The high dose of corticosteroids usually continues for a month,
and then the dose is slowly decreased.
• The rate at which you lower the dose may change if the patient
has recurring symptoms of GCA or large increases in the
sedimentation rate.
• In most cases, though, the prednisone dose can be reduced to
about 5 – 10 mg per day over a few months.
• Patients are usually tapered off this medicine by one to two years.
GCA rarely returns after treatment.

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Giant cell arteritis.pptx111111111111111

  • 3. VASCULITIS VASCULITIS(Pauci immune complexes) Primary or Secondary Systemic or Cutaneous Large vessel- Giant Cell arteritis, Takayasu Medium vessel-Polyarteritis nodosa, Behcet’s Disease, Kawasaki Small vessel(AASV)- Wegeners Granulomatosis, Churg-Strauss, Microscopic Polyangiitis. Secondary vasculitis- RA,SLE,HIV,HCV,HBV Syphilis,Drugs- (sulphonamides,ofloxacin),infections meningococcus,Staph,
  • 4.
  • 5. Introduction • Giant cell arteritis (GCA) is a disease of blood vessels, may occur together with polymyalgia rheumatica. • GCA occurs only in older adults, mainly those over age of 50, and can cause swelling and thickening of the small artery under the skin called the temporal artery. • A new, persisting headache is a common symptom of GCA. Symptoms of GCA promptly improve with corticosteroids. • If GCA affects blood flow to the eye, loss of vision can occur. Prompt detection and treatment of GCA can prevent loss of vision.
  • 6.
  • 7. • GCA is a type of vasculitis or arteritis, a group of diseases whose main feature is inflammation of blood vessels. • In GCA, the vessels most often involved are the arteries of the scalp and head, especially the arteries over the temples, which is why another term for GCA is “temporal arteritis.”
  • 8. Symptoms • Persistent, severe head pain, usually in your temple area • Scalp tenderness • Jaw pain when you chew or open your mouth wide • Fever • Fatigue • Unintended weight loss • Vision loss or double vision, particularly in people who also have jaw pain • Sudden, permanent loss of vision in one eye( however proper treatment can prevent this complication.)
  • 9. Diagnosis • There is no simple blood test or non invasive way to confirm the diagnosis of GCA. • The erythrocyte sedimentation rate (or sed rate) is a blood test that measures inflammation by checking to see how the rate at which red blood cells (erythrocytes) sediment (or fall) within an hour. • This rate is high in most people with GCA.
  • 10. Diagnosis • It is common to do a biopsy – or surgical removal – of a small piece of the temporal artery and study it under a microscope for signs of inflammation. • This biopsy is an outpatient procedure, done under local anesthesia (numbing of that site while you are awake). It leaves just a small scar that usually cannot be seen at the hairline in front of the ear. • In GCA, the biopsy shows inflammation of the artery
  • 11. Management • The treatment for GCA should begin as soon as possible because of the risk of loss of vision. • If you doctor strongly suspects GCA, treatment can start before you get the results of a temporal artery biopsy. • GCA treatment usually involves high doses of corticosteroids. Typically, the dose is 40-60 milligrams (mg) per day of prednisone . Headaches and other symptoms quickly decrease with treatment, and the sedimentation rate declines to a normal range.
  • 12. Mgt Contd • The high dose of corticosteroids usually continues for a month, and then the dose is slowly decreased. • The rate at which you lower the dose may change if the patient has recurring symptoms of GCA or large increases in the sedimentation rate. • In most cases, though, the prednisone dose can be reduced to about 5 – 10 mg per day over a few months. • Patients are usually tapered off this medicine by one to two years. GCA rarely returns after treatment.