path blood vessels - formatted Flashcards
- 72.APRIL02 You are asked for advice on screening for cerebral berry aneurysms. Which of the following conditions has THE LEAST risk of aneurysm of the circle of Willis?
- Neurofibromatosis type 1
- Marfan Syndrome
- Coarctation of the aorta
- Adult/ [Autosomal dominant] Polycystic Kidney Disease
- Systemic Lupus Erythematosis
- Systemic Lupus Erythematosis - F -
Known associations include: ADPCKD, Ehlers-Danlos type 4, NF1, Marfans, FMD of extracranial arteries, coarctation of aorta, hypertension (in 54% of patients). Most are sporadic.
- 68.APRIL02 A 53-year-old female has increasing congestive cardiac failure and normal vessels at coronary angiography. As a child she suffered rheumatic fever. The cardiac valves most likely to be affected are:
- Aortic alone
- Mitral and aortic
- Mitral and pulmonic
- Aortic and pulmonic
- Tricuspid and mitral
- Mitral and aortic - T - Rheumatic heart disease is overwhelmingly the most frequent cause of mitral stenosis (99% of cases). In patients with rheumatic heart disease, the mitral valve alone is involved in 65 to 70% of the cases, mitral and aortic in about 25%. Similar but generally less severe fibrous thickenings and stenoses can occur in the tricuspid valve
- 66.APRIL02 A 12-year-old male dies after a motor vehicle accident. At autopsy, mutiple yellow elongated lesions are seen on the intima of his otherwise normal abdominal aorta. Which of the following statements about this entity IS LEAST correct?
- Coronary lesions are less common than aortic lesions
- They are composed of lipid-filled foam cells and T lymphocytes
- More common in Western children than in Africa
- Can be seen in children less than 1 year of age
- Not all progress to fibrous atheromatous plaques
- More common in Western children than in Africa - F - Fatty streaks occur in all children older than 10y regardless of geography, race, sex or environment.
- 66.APRIL02 + APRIL 2004 A 12-year-old male dies after a motor vehicle accident. At autopsy, multiple yellow elongated lesions are seen on the intima of his otherwise normal abdominal aorta. Which of the following statements about this entity IS LEAST correct? (JS)
- Coronary lesions are less common than aortic lesions - T - Coronary fatty streaks are less common than aortic, beginning to form in adolescence, and they occur at the same anatomic sites that are later prone to develop plaques
- They are composed of lipid-filled foam cells and T lymphocytes - T - composed of lipid-filled foam cells with T lymphocytes and extracellular lipid present in smaller amounts than in plaques
- More common in Western children than in Africa - F - Fatty streaks occur in all children older than 10y regardless of geography, race, sex or environment.
- Can be seen in children less than 1 year of age - T
- Not all progress to fibrous atheromatous plaques T - although fatty streaks may be precursors of plaques, not all fatty streaks are destined to become fibrous plaques or more advanced lesions)
- Fatty streaks are not significantly raised and thus do not cause any disturbance in blood flow.
- They may be precursors, however, of the more ominous atheromatous plaques.
- The streaks begin as multiple yellow; flat spots ( fatty dots) less than 1 mm in diameter that coalesce into elongated streaks; 1 cm long or longer.
- Fatty streaks are composed of lipid-filled foam cells with T lymphocytes and extracellular lipid present in smaller amounts than in plaques.
- Fatty streaks appear in the aortas of some children younger than 1 year of age and all children older than 10 years, regardless of geography, race, sex, or environment.
- Coronary fatty streaks are less common than aortic but begin to form in adolescence, and they occur at the same anatomic sites that are later prone to develop plaques.
- They subsequently decrease in number as atherosclerotic plaques become more prevalent.
- The relationship of fatty streaks to atherosclerotic plaques is complex. o Fatty streaks are related to the known risk factors of atherosclerosis in adults (especially serum lipoprotein cholesterol concentrations and smoking), and some experimental evidence supports the concept of the evolution of fatty streaks into plaques.
- Fatty streaks, however, often occur in areas of the vasculature that are not particularly susceptible to developing atheromas later in life.
- Moreover, they frequently affect individuals in geographic locales and populations in which atherosclerotic plaque is uncommon.
- Thus, although fatty streaks may be precursors of plaques, not all fatty streaks are destined to become fibrous plaques or more advanced lesions.
Atherosclerosis
1) define
2) modiafiable factors
3) non-modifiable factors
4) describe fatty streaks
5) list the step of atherosclerosis
1)
- chronic vascular disease
- accumulation of cholesterol within the wall of the vessel causing progressive narrowing
2)
- smoking, drinking
- obesity
- DM
- hypertension
3) - age- sex- familial - genetics
4)
a) Fatty dots in intima
b) coalesce to call fatty streaks- foamy cells and cholesterol, less compared to an atheroma
- can occur in children
- aorta 1st, then all children have it by 10 years
- coronary artery in adolescent
- not all progress onto atheroma
5)
A) LDL move into intima- by vascular damage (smoking, hypertension)
b) oxidised LDL release cytokines- release MCP (monocyte attractant protein)
-> attract SM and monocyte- release M-CSF (macrophage stimulating factors)
-> change monocyte to macrophage
-> macrophage injest LDL
-> becomes foamy macrophage
Foamy cell-> cause SM proliferation
- > enlarging atheroma develop
- thin fibrous capsule
- eventually ruptures then clots with platelets and thrombin
- repeated rupture narrows lumen
- 62.APRIL02 Which of the following IS NOT correct regarding polyarteritis nodosa?
- There is a transmural necrotising vasculitis of small to medium size arteries
- There is associated glomerulonephritis
- There is sparing of the pulmonary circulation
- It is associated with Hepatitis B antigen positivity in over 20% of cases
- Remission or cure is achieved in 90% with steroid and cycle
- There is associated glomerulonephritis - F - Renal involvement is one of the prominent manifestations, BUT because there is no small vessel involvement, glomerulonephritis is not present.
- 62.APRIL02 Which of the following IS NOT a correct regarding polyarteritis nodosa? (JS)
- There is a transmural necrotising vasculitis of small to medium size arteries - T - Systemic vasculitis manifested by transmural necrotizing inflammation of small or medium-sized muscular arteries, typically renal and visceral, sparing pulmonary circulation. The common manifestations are malaise, fever,weight loss, hypertension, abdominal pain, malaena, muscle aches, peripheral neuritis. Little association with ANCA. Angiography shows aneurysms or occlusions of the main visceral arteries in 50% of cases. (Robbins)
- There is associated glomerulonephritis - F - Renal involvement is one of the prominent manifestations, BUT because there is no small vessel involvement, glomerulonephritis is not present.
- There is sparing of the pulmonary circulation - T
- It is associated with Hepatitis B antigen positivity in over 20% of cases - T - 30% patients have hepatitis B antigen in serum
- Remission or cure is achieved in 90% with steroid and cyclophosphamide - T - Disease is fatal if untreated but therapy is very effective.
SOh: PAN- Systemic vasculitis causing necrotizing inflammation of small and medium-sized vessels, resulting in microaneurysms, occlusions, and strictures. Acute renal failure, HTN, perirenal hematoma. GN not seen in PAN.
c.f. Microscopic polyangiitis: small arterioles and capillaries. Necrotizing GN (90%) and pulmonary capillaritis. No microaneurysms.
63.APRIL02 Which of the following would be an UNEXPECTED finding following coronary angioplasty?
- Luminal expansion
- Plaque rupture
- Thickened intact intima
- Medial dissection
- Proliferative restenosis in 30-50% of patients at 6 months
- Thickened intact intima - F - The split encompasses the intima and media
- 63.APRIL02 Which of the following would be an UNEXPECTED finding following coronary angioplasty? (JS)
- Luminal expansion - T - The key elements of luminal expansion in angioplasty are plaque rupture, medial dissection and stretching of the media of the dissected segment.
- Plaque rupture - T
- Thickened intact intima - F - The split encompasses the intima and media
- Medial dissection - T
- Proliferative restenosis in 30-50% of patients at 6 months - T -
The long-term success of angioplasty is limited by the development of proliferative restenosis that occurs in approximately 30 to 50% of patients within the first 4 to 6 months after angioplasty
• The process of balloon dilation of an atherosclerotic vessel characteristically causes plaque fracture, often with accompanying localized hemorrhagic dissection of the adjacent arterial wall.
• The plaque splits at its weakest point, which is not necessarily the area most severely obstructed.
• The key elements of luminal expansion in angioplasty are plaque rupture, medial dissection, and stretching of the media of the dissected segment, leading to local flow abnormalities and generation of new, potentially thrombogenic blood-contacting surfaces.
• Thus, an atherosclerotic plaque after angioplasty is unstable, having many features of the disrupted plaque associated with the acute coronary syndromes and other complications of atherosclerosis
• Uncommonly, abrupt reclosure follows the angioplasty. o This reclosure usually occurs as a result of compression of the lumen by an extensive circumferential or longitudinal dissection or by thrombosis.o Nevertheless, most patients improve symptomatically after angioplasty, thereby avoiding the need for aortocoronary bypass graft surgery at that time.
• The long-term success of angioplasty is limited by the development of proliferative restenosis that occurs in approximately 30 to 50% of patients within the first 4 to 6 months after angioplasty
- 64.APRIL02 A 33-year-old woman has sudden onset of blindness in her left eye. The multislice CT angiogram shows marked diffuse narrowing of her brachiocephalic, subclavian and common carotid arteries. There is also involvement both of her external and internal carotid arteries. This distribution is most suggestive of:
- Takayasu arteritis
- Atherosclerosis associated with familial
hypercholesterolaemia - Giant cell arteritis
- Polyarteritis nodosa
- Fibromuscular hyperplasia
- Takayasu arteritis - T - clinical syndrome characterized principally by ocular disturbances and marked weakening of the pulses in the upper extremities (pulseless disease), related to fibrous thickening of the aortic arch with narrowing or virtual obliteration of the origins or more distal portions of the great vessels arising in the arch. It has been reported in most areas of the world, including the United States. The illness is seen predominantly in women younger than 40 years old6.
- APRIL02 A 33-year-old woman has sudden onset of blindness in her left eye. The multislice CT angiogram shows marked diffuse narrowing of her brachiocephalic, subclavian and common carotid arteries. There is also involvement both of her external and internal carotid arteries. This distribution is most suggestive of: (JS)
- Takayasu arteritis - T - clinical syndrome characterized principally by ocular disturbances and marked weakening of the pulses in the upper extremities (pulseless disease), related to fibrous thickening of the aortic arch with narrowing or virtual obliteration of the origins or more distal portions of the great vessels arising in the arch. It has been reported in most areas of the world, including the United States. The illness is seen predominantly in women younger than 40 years old
- Atherosclerosis associated with familial hypercholesterolaemia - F - causes premature atherosclerosis in the same distribution as non-familial cases (ie abdominal aorta, ostia of major branches, coronary arteries, popliteal, descending thoracic, ICA and circle of Willis)
- Giant cell arteritis - F - most common of the vasculitides, is an acute and chronic, often granulomatous, inflammation of medium-sized and small arteries. It affects principally the arteries in the head– especially the temporal arteries– but also the vertebral and ophthalmic arteries. The latter may lead to blindness. In other expressions of this disorder, lesions have been found in arteries throughout the body, and in some cases the aortic arch has been involved to produce so-called giant cell aortitis. The disease is most common in older individuals and rare before the age of 50
- Polyarteritis nodosa - F - necrotising inflammation of medium sized or small arteries without GN or vasculitis within arterioles, capillaries or venules.
- Fibromuscular hyperplasia - F - proliferation of the muscular and fibrous elements in middle and large sized arteries of unknown aetiology. Affects renal arteries, ICA or vertebral, iliac, visceral.
- 10.02.11 Which of the following conditions IS NOT a cause (or association) of dissection ?
- Hypertension
- Arteriosclerosis
- Pregnancy
- Marfan’s syndrome
- Cystic medial degeneration
- Arteriosclerosis - F - medial scarring obstructs advancement of a dissecting aneurysm.
- 02.11 Which of the following conditions IS NOT a cause (or association) of dissection ? Rob 341 (JS)
- Hypertension - T - more than 90% of cases
- Arteriosclerosis - F - medial scarring obstructs advancement of a dissecting aneurysm
- Pregnancy - T - for unknown causes occurs shortly after pregnancy
- Marfan’s syndrome - T - and other connective tissue disorders (Ehlers-Danlos syndrome, Turner’s) are associated with Cystsic Medial Degeneration
- Cystic medial degeneration - T - CMD consists of elastic fragmentation and separation of the elastic and fibromuscular elements of the tunica media. This is the most frequently preexisting histologically detectable lesion in dissection but it can be found incidentally at autopsy in patients free from dissection.
- 10.03.18 Patient A has dissection involving ascending aorta, Patient B has dissection involving ascending aorta, arch and descending aorta
- Both have type A
- Both have type B
- Patient A has type A and patient B has type B
- Patient A has DeBakey III and patient B has type B
- Patient A has DeBakey I and patient B has DeBakey III
- Both have type A
- 10.02.21 Kawasaki disease – which of the following is FALSE?
- Mostly occur in children younger than 2 years of age
- Is self-limited disorder with less than 1% death rate
- > 20% develop CVS sequale
- characterised by recurrent attacks
- characterised by recurrent attacks - F - Kawasaki syndrome is an arteritis involving large, medium and small arteries (often coronaries), associated with the mucocutaneous lymph node syndrome (fever, conjunctival and oral erythema and erosion, oedema of hands and feet, rash and cervical lymph nodes), usually in young children and infants. It is self limited.
- 10.02.21 Kawasaki disease – which of the following is FALSE? Rob p350 (JS)
- Mostly occur in children younger than 2 years of age - T - occurs in young children and infants with 80% younger than 4 years of age
- Is self-limited disorder with less than 1% death rate - T - acute fatalities occur in 1% of patients owing to coronary arteritis with superimposed thrombosis or ruptured coronary artery aneurysm
- > 20% develop CVS sequale - T - approximately 20% develop CVS sequelae including vasculitis of coronary arteries, ectasia, aneurysm formation with rupture, thrombosis, MI or sudden death
- characterised by recurrent attacks - F - Kawasaki syndrome is an arteritis involving large, medium and small arteries (often coronaries), associated with the mucocutaneous lymph node syndrome (fever, conjunctival and oral erythema and erosion, oedema of hands and feet, rash and cervical lymph nodes), usually in young children and infants. It is self limited.
KAWASAKI SYNDROME (MUCOCUTANEOUS LYMPH NODE SYNDROME)
• arteritis involving large, medium-sized, and small arteries (often the coronary arteries)• associated with the mucocutaneous lymph node syndrome, usually in young children and infants (80% younger than 4 years old).
• The acute illness is manifested by fever, conjunctival and oral erythema and erosion, edema of the hands and feet, erythema of the palms and soles, a skin rash often with desquamation, and enlargement of cervical lymph nodes
• It is usually self-limited
• Epidemic in Japan, the disease has also been reported in Hawaii and increasingly in the United States
• Approximately 20% of patients develop cardiovascular sequelae, with a range of severity from asymptomatic vasculitis of the coronary arteries, coronary artery ectasia, or aneurysm formation to giant coronary artery aneurysms (7 to 8 mm) with rupture or thrombosis, myocardial infarction, or sudden death.
• Kawasaki syndrome is the leading cause of acquired heart disease in children in the United States
• Acute fatalities occur in approximately 1% of patients owing to coronary arteritis with superimposed thrombosis or ruptured coronary artery aneurysm.
• Pathologic changes outside the cardiovascular system are rarely significant.
• Although the vasculitis resembles that of polyarteritis nodosa, with necrosis and pronounced inflammation affecting the entire thickness of the vessel wall, fibrinoid necrosis is usually less prominent in Kawasaki syndrome
- 10.02.31 What is the COMMONEST LESION/ SYSTEM involved in Wegener’s granulomatosis?
- Lungs
- Nasal cavity
- Kidneys
- Skin
- Paranasal sinus
- Lungs - T - persistent pneumonitis with bilateral nodular and cavitary infiltrates (95%)
- 10.02.31 What is the COMMONEST LESION/ SYSTEM involved in Wegener’s granulomatosis? Rob p351 (JS)
- Lungs - T - persistent pneumonitis with bilateral nodular and cavitary infiltrates (95%)
- Nasal cavity - F - mucosal ulceration of the nasopharynx (75%)
- Kidneys - F - evidence of renal disease (80%).
- Skin - F - Other features include skin rashes, muscle pain, articular involvement, mono or polyneuritis, fever
- Paranasal sinus - F - chronic sinusitis (90%)
- 10.02.73 Features of cystic lymphangioma do NOT include ?
- axillary location
- child 18 months old
- large cystic spaces
- benign lesion
- encapsulated
encapsulated - F - The margins of the tumor are not discrete, and these lesions are not encapsulated. Their removal can therefore be difficult.
- 10.02.73 Features of cystic lymphangioma do NOT include ? Rob p357
- axillary location - T - Almost invariably occur in children in the neck or axilla (rarely retroperitoneal)
- child 18 months old - T - Lymphangiomas are congenital malformations with 50-65% present at birth and 80-90% evident by 2 years
- large cystic spaces - T - made up of massively dilated cystic spaces lined by endothelial cells and separated by scant connective tissue stroma
benign lesion - T
encapsulated - F - The margins of the tumor are not discrete, and these lesions are not encapsulated. Their removal can therefore be difficult.
- Sep03.03 Which finding makes it less likely to be Wegener’s granulomatosis?
- lack of sinus involvement.
- Negative for cANCA
- Lack of renal involvement
- Negative for cANCA - T - cANCA is positive in 90% of patients with active generalised disease and has a specificity of 99% (according to Dahnert).
* Robbins says positive in up to 95% - Sep03.03 Which finding makes it less likely to be Wegener’s granulomatosis? (JS)
- lack of sinus involvement - F - 90% show chronic sinusitis
- Negative for cANCA - T - cANCA is positive in 90% of patients with active generalised disease and has a specificity of 99% (according to Dahnert)
- Lack of renal involvement - F - 80% show evidence of renal disease
- Sep03.47 Aortic dissection.
- Can occur without an intimal flap
- Longitudinal
- 30-50cm long
- aortic valve prevents involvement coronary arteries
- Can occur without an intimal flap - T - There is usually (but not always) an intimal tear that extends into but not through the media of the ascending aorta (Robbins). According to Primer, intimal flap is detectable in 85-90%.
- Sep03.47 + APRIL 2004 Aortic dissection. (JS)
- Can occur without an intimal flap - T - There is usually (but not always) an intimal tear that extends into but not through the media of the ascending aorta (Robbins). According to Primer, intimal flap is detectable in 85-90%.
- Longitudinal - F - tears are usually transverse or oblique, 1-5cm in length with sharp jagged edges
- 30-50cm long - F - I presume they mean the length of the tear (1-5cm) or the length of the dissection which is variable
- Aortic valve prevents involvement coronary arteries - F - occlusion of coronary aa in 8%
- PATH2004 Which of the following statements with regards to fatty plaques is LEAST CORRECT?
- frequently affect individuals in geographic locales and populations in which atherosclerotic plaque is uncommon.
- ?% of kids that have them
- ?site
- bld vess and heart pg 503 blue box know well
- frequently affect individuals in geographic locales and populations in which atherosclerotic plaque is uncommon. (T)
- PATH2004 Which of the following statements with regards to fatty plaques is LEAST CORRECT? (–)
- frequently affect individuals in geographic locales and populations in which atherosclerotic plaque is uncommon. (T)
- ?% of kids that have them (some younger than 1, all older than 10 yoa)
- ?site (aorta more common than coronary arteries)
- bld vess and heart pg 503 blue box know well
• Fatty streaks are not significantly raised and thus do not cause any disturbance in blood flow.
• They may be precursors, however, of the more ominous atheromatous plaques.
• The streaks begin as multiple yellow; flat spots ( fatty dots) less than 1 mm in diameter that coalesce into elongated streaks; 1 cm long or longer.
• Fatty streaks are composed of lipid-filled foam cells with T lymphocytes and extracellular lipid present in smaller amounts than in plaques.
• Fatty streaks appear in the aortas of some children younger than 1 year of age and all children older than 10 years, regardless of geography, race, sex, or environment.
• Coronary fatty streaks are less common than aortic but begin to form in adolescence, and they occur at the same anatomic sites that are later prone to develop plaques.
• They subsequently decrease in number as atherosclerotic plaques become more prevalent.
• The relationship of fatty streaks to atherosclerotic plaques is complex.
o Fatty streaks are related to the known risk factors of atherosclerosis in adults (especially serum lipoprotein cholesterol concentrations and smoking), and some experimental evidence supports the concept of the evolution of fatty streaks into plaques.
• Fatty streaks, however, often occur in areas of the vasculature that are not particularly susceptible to developing atheromas later in life.
• Moreover, they frequently affect individuals in geographic locales and populations in which atherosclerotic plaque is uncommon.
Thus, although fatty streaks may be precursors of plaques, not all fatty streaks are destined to become fibrous plaques or more advanced lesions.