Mohammad Reza Shakibi M.D Kerman university of medical sciences (KMU) Shafa Hospital, Rheumatology ward

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VASCULITIS SYNDROMES Mohammad Reza Shakibi M.D Kerman university of medical sciences (KMU) Shafa Hospital, Rheumatology ward

ILLUSTRATED CASE 1 A 56 years old lady refered me for prolonged fever, arthritis and burning pain in her foots and hands. She had history of transfusion during operation 5 years ago and HBV infection. She had history of 3 month fever, fatigue, loss of appetite, postprandial abdominal pain and 5 Kg weight loss during this time. She also had arthritis in hand joints and severe burning pain in foots and hands. She noticed inability to extent left wrist.

ILLUSTRATED CASE 1 (CONTINUE) Her Ph/Exam showed : Fever, arthritis, wrist drop, gangrene g in finger tips.

ILLUSTRATED CASE 1 (CONTINUE) She diagnosed vasculitis and treatment started. Two days later she had sever abdominal pain and operation showed massive intestinal gangrene. She die 2 days later.

WHAT IS VASCULITIS? Vasculitis is a clinicopathologic process characterized by inflammation of and damage to blood vessels. The vessel lumen is usually compromised, and this is associated with ischemia of the tissues supplied by the involved vessel. A broad and heterogeneous group of syndromes may result from this process, since any type, size, and location of blood vessel may be involved. Vasculitis and its consequences may be the primary or sole manifestation of a disease; alternatively, vasculitis may be a secondary component of another primary disease. Vasculitis may be confined to a single organ, such as the skin, or it may simultaneously involve several organ systems.

POTENTIAL MECHANISMS OF VESSEL DAMAGE IN VASCULITIS SYNDROMES Pathogenic immune complex formation and/or deposition Henoch-Schönleinpurpura Vasculitis associated with collagen vascular diseases Serum sickness and cutaneous vasculitis syndromes Hepatitis C associated essential mixed cryoglobulinemia Hepatitis B associated polyarteritis nodosa Production of antineutrophilic cytoplasmic antibodies Wegener's granulomatosis Churg-Strauss syndrome Microscopic polyangiitis Pathogenic T lymphocyte responses and granuloma formation Giant cell arteritis Takayasu's arteritis Wegener's granulomatosis Churg-Strauss syndrome

VASCULITIS CLINICAL MANIFESTATIONS Systemic symptoms Constitutional symptoms: fever, weight loss, malaise, arthralgias/arthritis, loss of appetite, generals body pain Localized symptoms (According vessel size ) Large Vessel Vasculitides Medium Vessel Vasculitides Small Vessel Vasculitides

Vasculitis Clinical manifestations Large Vessel Vasculitides Limb claudication Asymmetric blood pressures Absence of pulses Bruits Aortic dilation Renovascular hypertension

Vasculitis Clinical manifestations Large Vessel Vasculitides Takayasu arteritis (TAK) Giant cell arteritis (GCA)

Vasculitis Clinical manifestations Medium Vessel Vasculitides Cutaneous nodules Ulcers Livedo reticularis i Digital gangrene Mononeuritis multiplex Microaneurysms Renovascular hypertension

Vasculitis Clinical manifestations Medium Vessel Vasculitides Polyarteritis nodosa (PAN) Kawasaki disease (KD)

Vasculitis Clinical manifestations Small Vessel Vasculitides Purpura Vesiculobullous lesions Uti Urticariai Glomerulonephritis Alveolar hemorrhage Cutaneous extravascular necrotizing granulomas Splinter hemorrhages Uveitis/episcleritis/scleritis

Vasculitis Clinical manifestations Small Vessel Vasculitides Antineutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) Microscopic polyangiitis (MPA) Granulomatosis with polyangiitis (Wegener s) (GPA) Eosinophilic granulomatosis with polyangiitis (Churg- Strauss) (EGPA) Immune complex SVV Anti glomerular basement membrane (anti-gbm) disease Cryoglobulinemic vasculitis (CV) IgA vasculitis (Henoch-Scho nlein) nlein) (IgAV) Hypocomplementemic urticarial vasculitis (HUV) (anti-c1q vasculitis)

PANCA PATTERN

CANCA PATTERN

DIFFERENTIAL DIAGNOSIS FOR PRIMARY SYSTEMIC VASCULITIS Infection Endocarditis Sepsis Syphilis Meningococcemia Viral hepatitis Tuberculosis Disorders of Coagulation Disseminated intravascular coagulation Antiphospholipid p p antibody syndrome Thrombotic thrombocytopenic purpura Drug Toxicity Sympathomimetic ti agents Cocaine

DIFFERENTIAL DIAGNOSIS FOR PRIMARY SYSTEMIC VASCULITIS Atherosclerotic and Embolic Disease Peripheral vascular disease Cholesterol embolization syndrome Generalized atherosclerosis Cardiac myxomas Malignancy Lymphoma Disseminated i carcinomatosis i Secondary Vasculitides Associated with Other Autoimmune Conditions Systemic lupus erythematosus Sjögren syndrome Rheumatoid arthritis Behçet disease Sarcoidosis

DIFFERENTIAL DIAGNOSIS FOR PRIMARY SYSTEMIC VASCULITIS Congenital Abnormalities and Anatomic Variants Fibromuscular dysplasia Ehlers-Danlos syndrome Marfan syndrome Other Disorders Buerger disease Calciphylaxis Amyloidosis