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Polymyalgia Rheumatica (PMR) Temporal Arteritis (TA)
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Diagnostic Criteria- PMR (healey 1984) 1.Age> 50 yrs 2.Pain corresponding to proximal muscles of the limbs. 2 out of 3 regions: neck, shoulder & pelvic girdle. Symptoms> 1 month 3.Morning stiffness> 1 hr 4.Elevated ESR (>40 mm/hr) 5.Rapid response to low dose of steroids
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Diagnostic Criteria- TA (ACR 1990) 1.Age> 50 years 2.Recent localized headache 3.Temporal artery abnormality 4.Elevated ESR 5.Temporal biopsy positive for vasculitis * Diagnosis ≥ 3
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Epidemiology Central+north of Europe, north America Mainly Caucasian Women>men X2-3 Older age 90%> 60 years Annual prevalence: TA: 6.7/10 5 PMR: 53/10 5
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Etiology Genetic tendency (familial+ethnic). HLA-DR 4 Infectious agent? (Clusters of cases+annual variation) Immune response involving 2 processes: a.An immune response with presence of active mononuclear cells in peripheral blood (IL-6) +systemic symptoms. b.Granulomatotic inflammation with involvement of CMI against Ag in the inner elastic membrane or near
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Pathology 1.Lymphocytic infiltration (CD4) near the elastica 2.Thickening of the intima without prominent infiltration 3.Massive infiltration: lymphocytes+macrophages+giant cells+granulomas 4.Necrosis of the arterial wall 5.Thrombosis of blood vessels in inflamed areas 6.Recanalization
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Arteries Involved: - Superficial temporal, Vertebral, Posterior Ciliary, Ophtalmic - Central retinal, Carotid, Subclavian, Brachial, Aorta,
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Clinical Features The onset usually insidious I. Constitutional symptoms II. TA III. PMR
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I. Constitutional Symptoms 1.Fatigue, depression 2.Anorexia, weight loss (50%, 6 Kg) 3.Fever (50%) 15% of cases with FUO age>65 yrs TA
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II. Temporal Areteritis 1.Headache- often localized to temples or occiput (2/3). On physical exam: Nodular, thickened, tender vessel +absent or weak pulse 2.Ophthalmic manifestation: 20-50%. a. Diplopia b. Ptosis c. Visual loss: 6-10%. Usually sudden, painless and permanent. Fundus: Anterior>Posterior ischemic optic neuropathy
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II. Temporal Areteritis 3. Neurological manifestation: 30% a. Peripheral neuropathy b. Involvement of carotid or vertebrobasilar TIA, CVA 4. Jaw claudication 5. Sore throat 6. Hoarseness
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II. Temporal Areteritis 7. Occlusion of large as: 10-15%. a. Claudication of the hands. On exam: Bruits + weak pulses b. Raynaud phenomenon c. Aneurysm, dissection of thoracic aorta- late
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III. Polymyalgia Rheumatica 1.Arthralgia/myalgia. Usually starts in neck, shoulder +pelvic girdle Symetrical Infrequent distal involvement On exam: muscle strength usually unimpaired 2. Morning stiffness 3. Night pains 4. Tenderness of periarticular structures: capsule,bursa, tendon 5. +Mild & transient synovitis usually knees, wrists, SCJ
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Relationship between PMR & TA 1.Similar Age & sex & ethnic distribution 2.In both + systemic features 3.10-15% of PMR have positive temporal biopsies 4.Good response to steroids 5.40-60% of TA patients +PMR 6.20-40% of TA patients PMR is the presenting symptoms * PMR may precede, coincide with or follow TA
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Investigations 1.ESR 2.Anemia-normocytic, mild to moderate 3.ILFT- 30%, ALP (70%) 4.RF, ANA- negative 5.Doppler of temporal as 6.CT, MRI if involvement of large as is suspected 7.Temporal biopsy
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Differential Diagnosis 1.Malignancy a. Solid tumors b. Hematological malignancy: MM, Leukemia, Lymphoma 2. Joint diseases a. OA, especially +cervical involvement b. RA c. Collagen vascular diseases
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Differential Diagnosis 3. Muscles diseases a. Polymyositis b. Myopathy 4. Chronic infections a. SBE b. osteomyelitis 5. Hypothyroidism 6. Parkinson disease 7. Functional
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Treatment 1.Steroids a. Initial dose PMR: 10-20 mg of prednisone per day TA: 40-60 mg per day +Eye involvement: Pulse IV methylprednisolone 1 gr X 3 ds b. Gradual decease of steroids dose 2. Steroid sparing agents: Methotrexate
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