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Презентация на тему Takayasu’s arteritis

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EpidemiologyMore case reports from Japan ,India, South-east Asia, MexicoNo geographic restrictionNo race – immuneIncidence-2.6/million/year-N.America/EuropeThe incidence in Asia is 1 case/1000-5000 women.
TAKAYASU’S ARTERITISDr Katya Dolnikov2017D_katya@rambam.health.gov.il EpidemiologyMore case reports from Japan ,India, South-east Asia, MexicoNo geographic restrictionNo race AgeMc-2nd & 3rd decadeMay range from infancy to middle ageIndian studies-age HistopathologyIdiopathic inflammatory arteritis of elastic arteries resulting in occlusive/ ectatic changesLarge vessels Pathogenesis Antigen-driven disease, with the site of immunologic recognition events being the Pathological findings in Takayasu arteritis. Heather L. Gornik, and Mark A. Creager MacroscopicGelatinous plaques-earlyWhite plaques-collagenDiffuse intimal thickening  Superficial– deep scarring  circumferential MacroscopicWall thickening, fibrosis, stenosis, thrombus formation →end organ ischemiaMore inflammation → destroys MicroscopicPanarteritis with inflammatory mononuclear cell infiltrates within the vessel wall with frequent Clinical featuresEarly pre-pulseless/gen manifestationsFever, weight loss,headache, fatigue,malaise,night sweats, arthralgiaSplenomegaly, cervical, axillary lymphadenopathy CLINICAL MANIFESTATIONS Coronary involvement in TAOccurs in 10~30%Often fatalClassified into 3 typesType1:stenosis or occlusion Occular involvementHypertensive retinopathyCommonArteriosclerotic –art narrowing, av nipping,silver wiringNeuroretinopathy-exudates and papilloedemaDirect opthalmoscopyNonhypertensive retinopathyUYAMA nee Severe arteritis with complete occlusion of left carotid and subclavian artery. The long-segment diffuse stenotic involvement of the DTAafter deployment of stents. remission after treatment Figure 4. Takayasu arteritis involving the coronary ostia. Heather L. Gornik, and Figure 3. Aortic occlusive disease in a patient with Takayasu arteritis and Figure 7. Combination of 18F-FDG PET and CTA for assessment of Takayasu ostial stenosis of the right renal arteryafter deployment of a stent a/c phase-Axial T1-weighted image  wall thickening of As aorta and PAAxial Diagnosis The diagnosis of Takayasu's arteritis should be suspected strongly in a Treatment Disease-related mortality most often occurs from congestive heart failure, cerebrovascular events, Treatment of TA ・  Steroidsimmunosuppressants:Cyclosporine,Cyclophosphamide,Mtx,Mycophenolate mofetilAnti-platelet therapy(low-dose Aspirin)angioplasty/surgeryIf uncontrolledControl of vasculitisSymptomatic occlusionthrombosis Pharmacological treatment 0.7-1 mg/kg/day –prednisone for 1-3 monthscommon tapering regimen once remission↓ Steroids → 50% responseMethotrexate →further 50% respond25% with active disease will not Critical issue is in trying to determine whether or not disease is Invasive treatmentHTN with critical RASExtremity claudication limiting daily activitiesCerebrovascular ischaemia or critical
Слайды презентации

Слайд 2


Слайд 7 Epidemiology
More case reports from Japan ,India, South-east Asia,

EpidemiologyMore case reports from Japan ,India, South-east Asia, MexicoNo geographic restrictionNo

Mexico
No geographic restriction
No race – immune
Incidence-2.6/million/year-N.America/Europe
The incidence in Asia

is 1 case/1000-5000 women.


Слайд 8 Age
Mc-2nd & 3rd decade
May range from infancy

AgeMc-2nd & 3rd decadeMay range from infancy to middle ageIndian

to middle age
Indian studies-age 3- 50 y

Gender diff


Japan-F:M=8-9:1
India-F:M ratio varies from -1:1 - 3:1




Epidemiology


Слайд 9

Genetics

Japan - HLA-B52 and B39
Mexican and Colombian patients - HLA-DRB1*1301 and HLA-DRB1*1602
India- HLA- B 5, -B 21


Слайд 10 Histopathology
Idiopathic inflammatory arteritis of elastic arteries resulting in

HistopathologyIdiopathic inflammatory arteritis of elastic arteries resulting in occlusive/ ectatic changesLarge

occlusive/ ectatic changes
Large vessels – Aorta and its main

branches (brachiocephalic, carotid, SCL, vertebral, RA)
Coronary and PA involvement
Aorta - usually not beyond IMA
Multiple segments with skipped areas
or diffuse involvement


Слайд 11 Pathogenesis
Antigen-driven disease, with the site of immunologic

Pathogenesis Antigen-driven disease, with the site of immunologic recognition events being

recognition events being the adventitia.
DC in adventitia activated by

AG release IL-18 and chemokines that “recruit” T cells from vasa vasorum to the vessel wall
CD4+ T cells secrete interferon-γ→
stimulate macrophages and multinucleated giant cells
The results of this inflammatory cascade are :
granulomatous inflammation
destruction of the internal elastic lamina
arterial wall hyperplasia, smooth muscle cell proliferation, intimal thickening, vascular occlusion


Слайд 12 Pathological findings in Takayasu arteritis.
Heather L. Gornik,

Pathological findings in Takayasu arteritis. Heather L. Gornik, and Mark A.

and Mark A. Creager Circulation. 2008;117:3039-3051
Copyright © American Heart

Association, Inc. All rights reserved.

Слайд 13 Macroscopic
Gelatinous plaques-early
White plaques-collagen
Diffuse intimal thickening

Superficial– deep

MacroscopicGelatinous plaques-earlyWhite plaques-collagenDiffuse intimal thickening Superficial– deep scarring circumferential

scarring

circumferential stenosis
Mural thrombus
2⁰

atheromatous changes
long standing,
HTN






Слайд 14 Macroscopic

Wall thickening, fibrosis, stenosis, thrombus formation →end organ

MacroscopicWall thickening, fibrosis, stenosis, thrombus formation →end organ ischemiaMore inflammation →

ischemia
More inflammation → destroys arterial media → Aneurysm (fibrosis

inadequate)
Most patients with aneurysms also have stenosis


Слайд 15 Microscopic
Panarteritis with inflammatory mononuclear cell infiltrates within the

MicroscopicPanarteritis with inflammatory mononuclear cell infiltrates within the vessel wall with

vessel wall with frequent giant cell formation
There is proliferation

of the intima and fragmentation of the internal elastic lamina



Слайд 17 Clinical features
Early pre-pulseless/gen manifestations
Fever, weight loss,headache, fatigue,malaise,night sweats,

Clinical featuresEarly pre-pulseless/gen manifestationsFever, weight loss,headache, fatigue,malaise,night sweats, arthralgiaSplenomegaly, cervical, axillary

arthralgia
Splenomegaly, cervical, axillary lymphadenopathy
Late ischemic phase
Sequel

of occlusion of Ao arch/br
Diminished/absent pulses (84–96%)
Bruits (80–94%)
Hypertension (33–83% )
RAS(28–75%)

Слайд 18 CLINICAL MANIFESTATIONS

CLINICAL MANIFESTATIONS

Слайд 20 Coronary involvement in TA

Occurs in 10~30%
Often fatal
Classified into

Coronary involvement in TAOccurs in 10~30%Often fatalClassified into 3 typesType1:stenosis or

3 types

Type1:stenosis or occlusion of coronary ostia
Type2:diffuse or focal

coronary arteritis
Type3:coronary aneurysm

Слайд 21 Occular involvement
Hypertensive retinopathy
Common
Arteriosclerotic –art narrowing, av nipping,silver wiring
Neuroretinopathy-exudates

Occular involvementHypertensive retinopathyCommonArteriosclerotic –art narrowing, av nipping,silver wiringNeuroretinopathy-exudates and papilloedemaDirect opthalmoscopyNonhypertensive

and papilloedema
Direct opthalmoscopy
Nonhypertensive retinopathy
UYAMA & ASAYAMA CLASS
stage 1- Dil

of small vessels
stage 2- Microaneurysm
stage 3- Art-ven anastomoses
stage 4- Ocular complications






Слайд 24 Severe arteritis with complete occlusion of left carotid

Severe arteritis with complete occlusion of left carotid and subclavian artery.

and subclavian artery. The right subclavian artery is also

occluded

Слайд 25
long-segment diffuse stenotic involvement of the DTA
after deployment

long-segment diffuse stenotic involvement of the DTAafter deployment of stents.

of stents.


Слайд 26

remission after treatment

remission after treatment

Слайд 27 Figure 4. Takayasu arteritis involving the coronary ostia.

Figure 4. Takayasu arteritis involving the coronary ostia. Heather L. Gornik,


Heather L. Gornik, and Mark A. Creager Circulation. 2008;117:3039-3051
Copyright

© American Heart Association, Inc. All rights reserved.

Слайд 28 Figure 3. Aortic occlusive disease in a patient

Figure 3. Aortic occlusive disease in a patient with Takayasu arteritis

with Takayasu arteritis and bilateral leg claudication.
Heather L.

Gornik, and Mark A. Creager Circulation. 2008;117:3039-3051

Copyright © American Heart Association, Inc. All rights reserved.


Слайд 29 Figure 7. Combination of 18F-FDG PET and CTA

Figure 7. Combination of 18F-FDG PET and CTA for assessment of

for assessment of Takayasu arteritis.
Heather L. Gornik, and

Mark A. Creager Circulation. 2008;117:3039-3051

Copyright © American Heart Association, Inc. All rights reserved.


Слайд 30
ostial stenosis of the right renal artery

after deployment

ostial stenosis of the right renal arteryafter deployment of a stent

of a stent


Слайд 31
a/c phase-Axial T1-weighted image
wall thickening of

a/c phase-Axial T1-weighted image wall thickening of As aorta and PAAxial

As aorta and PA
Axial T1-weighted image- improvement of wall

thickening of As Ao and PA after steroid therapy

Слайд 33 Diagnosis

The diagnosis of Takayasu's arteritis should be suspected

Diagnosis The diagnosis of Takayasu's arteritis should be suspected strongly in

strongly in a young woman who develops a decrease

or absence of peripheral pulses, discrepancies in blood pressure, and arterial bruits.
The diagnosis is confirmed by the characteristic pattern on arteriography, which includes irregular vessel walls, stenosis, poststenotic dilation, aneurysm formation,

Слайд 34 Treatment
Disease-related mortality most often occurs from congestive

Treatment Disease-related mortality most often occurs from congestive heart failure, cerebrovascular

heart failure, cerebrovascular events, myocardial infarction, aneurysm rupture, or

renal failure.
The course of the disease is variable, and although spontaneous remissions may occur, Takayasu's arteritis is most often chronic and relapsing.
Glucocorticoid therapy for acute signs and symptoms.
An aggressive surgical and/or arterioplastic approach to stenosed vessels. Unless it is urgently required, surgical correction of stenosed arteries should be undertaken only when the vascular inflammatory process is well controlled with medical therapy.
In individuals who are refractory to or unable to taper glucocorticoids, methotrexate in doses up to 25 mg per week has yielded encouraging results.
Anti-TNF therapies have encouraging results

Слайд 35 Treatment of TA
 

  
Steroids
immunosuppressants:
Cyclosporine,Cyclophosphamide,
Mtx,Mycophenolate mofetil
Anti-platelet therapy(low-dose Aspirin)
angioplasty/surgery
If uncontrolled
Control of

Treatment of TA ・  Steroidsimmunosuppressants:Cyclosporine,Cyclophosphamide,Mtx,Mycophenolate mofetilAnti-platelet therapy(low-dose Aspirin)angioplasty/surgeryIf uncontrolledControl of vasculitisSymptomatic occlusionthrombosis

vasculitis
Symptomatic occlusion
thrombosis


Слайд 36 Pharmacological treatment

0.7-1 mg/kg/day –prednisone for 1-3 months

common

Pharmacological treatment 0.7-1 mg/kg/day –prednisone for 1-3 monthscommon tapering regimen once

tapering regimen once remission
↓ pred by 5 mg/week →

20 mg/day.
Thereafter, ↓by 2.5 mg/week → 10 mg/day
↓1 mg/day each week, as long as disease does not become more active
Pulse iv corticosteroids - CNS symptoms- no data to support

Слайд 37
Steroids → 50% response
Methotrexate →further 50% respond
25% with

Steroids → 50% responseMethotrexate →further 50% respond25% with active disease will

active disease will not respond to current treatments
resistant

to steroids/ recurrent disease once corticosteroids are tapered
cyclophosphamide (1-2 mg/kg/day),
azathioprine (1-2mg/kg/day), or
methotrexate (0.3 mg/kg/week)
Mycophenolate mofetil/ anti TNF α agents


Слайд 38
Critical issue is in trying to determine whether

Critical issue is in trying to determine whether or not disease

or not disease is active
During Rx- regular clinical examination

and ESR+ CRP initially - every few days
CT or MRA - 3 to 12 months - (active phase of Rx), and annually thereafter
Criteria for active disease


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