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57 Cards in this Set
- Front
- Back
resistance vessels (2)
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small arteries
arterioles |
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small arteries are ___ in diameter
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<2 mm
|
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in arterioles, ___ aren't identifiable
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3 layers
|
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vasculitis is ___. it can cause ___ to tissues
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inflammation of vessels causing luminal narrowing
ischemia |
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___ happens to an ischemic luminal organ
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ulceration
|
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3 causes of vasculitis
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immune complexes
cell mediated immunity anti-endothelial Abs |
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2 kinds of large artery vasculitis
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giant cell (temporal) arteritis
takayasu arteritis |
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giant cell arteritis is a ___ inflammation of ___. it only affects people over ___. it affects women ___ times more frequently than men.
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granulomatous
external branches of carotid a. 50 2.5 |
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T/F: giant cell arteritis is rare
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false
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giant cell arteritis most commonly affects ___ (3) arteries.
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temporal
vertebral ophthalmic |
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rarely, GCA can occur at ___ (3)
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coronaries
aorta GI arteries |
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if the ophthalmic artery is affected, ___ can result
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sudden blindness
|
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diagnosis of GCA is via ___
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biopsy
|
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treatment of GCA is with ___
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steroids
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any chronic inflammatory disease can cause ___
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anemia
|
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GCA presents with (6)
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headache
fever weakness weight loss elevated ESR polymyalgia rheumatica |
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takayasu's arteritis is aka (2)
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granulomatous-sclerosing aortitis
pulseless disease |
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TA is ___. it mostly affects ___ in ___.
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stenosing inflammation of aortic arch and tributaries
young women far east |
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TA presents with (3)
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ocular disturbances
weakened pulse in upper extremities neurologic disorders |
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2 kinds of medium artery vasculitis
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polyarteritis nodosa
kawasaki's disease |
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PAN is ___ attacking arteries to ___ (7).
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systemic vasculitis
kidneys heart liver GIT testes skeletal muscle PNS |
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PAN does not affect ___
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pulmonary arteries
|
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acute PAN lesions have (3)
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fibrinoid necrosis
inflammatory cells (neutrophils) in wall luminal thrombus |
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healing PAN lesions have
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intiimal fibroblast proliferation
chronic inflammatory cells (macrophages) |
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healed PAN lesions have (3)
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intimal fibrosis
medial fibrosis loss of elastica interna |
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T/F: all 3 lesions may be present in different segments of same artery
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true
|
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PAN mostly affects ___. It presents with ___ (7)
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young and middle aged people
fever fatigue weakness renal symptoms musculoskeletal symptoms GIT symptoms PNS symptoms |
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PAN lab findings
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normocytic anemia
elevated ESR 30%: HBsAg |
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PAN treatment (2)
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steroids
cyclophosphamide |
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PAN inflammation is more common at ___, where it can cause ___
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bifurcations
microaneurysm |
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PAN inflammation can trigger release of ___, which can cause.
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procoagulatory proteins
thrombosis |
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3 kinds of small vessel vasculitis
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ANCA associated
immune complex associated others |
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treatment for small vessel vasculitis (2)
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steroids
cyclophosphamide |
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3 kinds of ANCA-associated vasculitis
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microscopic polyangiitis
wegener's granulomatosis churg-strauss angiitis and granulomatosis |
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microscopic polyangiitis can be identified serologically by ___
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P-ANCA
|
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P-ANCA Abs are against
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MPO
|
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MP presents with (2)
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glomerulonephritis
pulmonary vasculitis |
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glomerulonephritis manifests as (3)
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hematuria
proteinuria renal failure |
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pulmonary vascultis manifests as (2)
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pneumonitis
hemoptysis |
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Wegener's granulomatosis presents with (3)
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necrotizing granulomas of respiratory tract
granulomatous vasculitis (RT and elsewhere) glomerulonephritis |
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T/F: WG is common
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false
|
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WG can be identified serologically by ___. these are Abs against
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C-ANCA
proteinase 3 |
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like MP, WG symptoms include ___ (2). they also include ___ (4)
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hemoptysis
renal failure arthritis neuritis rash myalgia |
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Churg-Strauss is associated with ___
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P-ANCA
|
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Churg-Strauss is aka ___. it is characterized by ___
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allergic angiitis
eosinophilis and granulomas of venules and capillaries |
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Churg-Strauss affects
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pulmonary vessels
nerves heart |
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3 kinds of immune complex associated vasculitis
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Henoch-Schönlein purpura
cryoglobulinemic purpura cutaneous leukocytoclastic vasculitis |
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Henoch-Schönlein presents with (4)
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purpura
arthralgia colicky abdominal pain 50%: renal symtpoms |
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T/F: Henoch-Schönlein has a good prognosis
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true
|
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Henoch-Schönlein usually follows ___. It is most common in ___ age ___
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URTI
children 3-8 |
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cryoglobulinemic purpura presents with (3)
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purpura
arthralgia glomerulonephritis |
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cryoglobulinemic purpura is usually associated with ___
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HCV
|
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CP serum has ___ and low ___ (2)
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cryoglobulins
C3 C4 |
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in cutaneous leukocytoclastic vasculitis, ___ infiltrates ___ (2). ___ may also be present.
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neutrophils
venules capillaries fibrinoid necrosis |
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CLV presents with and has 3 kinds of etiologies:
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palpable purpura
idiopathic iatrogenic infective |
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treatment for CLV is ___
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symptomatic
|
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non-ANCA, non-immune related causes of small vessel vasculitis (2)
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paraneoplastic
IBD |