Cardiothoracic Flashcards

(237 cards)

1
Q

What are the imaging features of sarcoidosis?

A

Bilateral hila + right paratracheal lymph nodes

Perilymphatic nodules with upper lobe predominance

Late : upper lobe fibrosis + traction bronchiectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the causes of right heart failure?

A

Left heart failure (most common)

Chronic PE

Right-sided valve issues (tricuspid regurgitation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Interstitial lung disease related to smoking with poorly defined apical centrilobular nodules

A

Respiratory bronchiolitis-interstitial lung disease

(RB-ILD)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the most common interstitial lung disease in scleroderma?

A

Non-specific interstitial penumonia

(NSIP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Interstitial lung disease with lower lobe, peripheral predominance and sparing of the immediate subpleural lung.

A

Non-specific interstitial pneumonia

(NSIP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the differential for perilymphatic pulmonary nodules?

A

Sarcoidosis (90%)

Silicosis

Lymphangitic spread of cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How can you differentiate between cancer and progressive massive fibrosis on MRI?

A

Cancer = T2 bright

PMF = T2 dark

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Silicosis increases your risk of which infection?

A

TB

(by 3-fold)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Which type of emphysema is seen in alpha-1-antitrypsin deficiency?

A

Panlobular with lower zone predominance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Which of the following options is negative on thallium201 scan?

  1. Kaposi 2. Lymphoma 3. PCP
A
  1. PCP
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Which of the following options is negative on gallium67 scan?

  1. Kaposi 2. Lymphoma 3. PCP
A
  1. Kaposi
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Which of the following options is positive on both gallium67 and thallium201 scan?

  1. Kaposi 2. Lymphoma 3. PCP
A
  1. Lymphoma
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Lymphocytic interstitial pneumonitis (LIP) is associated with which conditions?

A

Sjogren’s (most common)

HIV ← answer if in a child

SLE

RA

Castleman

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Birt Hogg Dube cystic lung disease has what kind of cysts?

A

Thin-walled oval cysts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Lymphangiomyomatosis (LAM) is associated with which kind of pleural effusions?

A

Chylous

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the most common cardiac manifestation of tuberous sclerosis?

A

Rhabdomyoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Lymphangiomyomatosis (LAM) is associated with which phakomatosis?

A

Tuberous sclerosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What are the patient and radiology characteristics of Langerhan’s cell histiocytosis (LCH)?

A

Smokers aged 20-30

Centrilobular nodules with upper lobe predominance which cavitate into cysts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Which conditions classically spare the costophrenic angles?

A

Langerhans cell histiocytosis (LCH)

Hypersensitivity pneumonitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Extralobar sequestration is associated with which other anomalies?

A

Congenital cystic adenomatoid malformation (CCAM)

Congenital diaphragmatic hernia

Vertebral anomalies

Congenital heart disease

Pulmonary hypoplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Which lung segment is most common segment for intralobar pulmonary sequestration?

A

Posterior segment of the left lower lobe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Which condition, intralobar or extralobar sequestration, presents in adolescence or adulthood with recurrent pneumonia?

A

Intralobar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Which condition, intralobar or extralobar sequestration presents in infancy with respiratory compromise?

A

Extralobar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Poland syndrome results in aplasia/hypoplasia of pec major (most common), pec minor, 2-5th ribs and breast/nipple. What other associations are there?

A

Upper limb abnormalities (small hand + brachysyndactyly, simian crease)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Where does a persistent left SVC normally drain?
Coronary sinus
26
What syndrome is associated with pulmonary arteriovenous malformations (AVM)?
Hereditary haemorrhagic telangiectasia | (Osler-Weber-Rendu syndrome)
27
Which lung segment is most commonly involved in bronchial atresia?
Apical-posterior segment of the left upper lobe
28
AIDs patient with lung nodules, pleural effusion and lymphadenopathy. What is the most likely diagnosis?
Lymphoma (almost exclusively high grade NHL, CD4 \< 100)
29
Carcinoid heart disease can occur in which cancers _without_ liver metastases?
Bronchial carcinoid tumour Ovarian carcinoid tumour
30
What scan can be carried out to localise a carcinoid tumour?
Octreotide scan
31
Which cardiac valves can be affected in GI carcinoid syndrome?
Tricuspid & pulmonary
32
Which cancers can cause the classic “cannonball” metastases?
Renal cell Choriocarcinoma (testicle)
33
Which cancers cause lymphangitic calcinomatosis?
Bronchogenic (most common) Breast Stomach Pancreas Prostate
34
What is the bacterium responsible in the majority of cases of Lemierre syndrome?
Fusobacterium necrophorum
35
What is the syndrome characterised by seropositive rheumatoid arthritis and pulmonary fibrosis?
Caplan syndrome
36
Fungal infection with invasion of the mediastinum, pleura & chest wall?
Mucormycosis
37
What are the 6 major criteria for ABPA?
Asthma Central bronchiectasis Pulmonary opacities (transient or chronic) Blood eosinophilia Skin reactivity to Aspergillus antigen Increase serum IgE
38
What is the treatment for immune reconstitution inflammatory syndrome?
Steroids
39
What are the risk factors for immune reconstitution inflammatory syndrome?
Low CD4 count (\< 50) High plasma HIV RNA (before therapy) Rapid decrease in CD4 count of HIV RNA following initiation of therapy Initiation of HAART soon after diagnosis. of an opportunistic infection (TB, PML, cryptococcus, Kaposi)
40
A patient with AIDs is started on antiretroviral therapy. 1 month later they have worsening symptoms despite improvements in CD4 counts and falling viral load. What is the diagnosis?
Immune reconstitution inflammatory syndrome (IRIS)
41
An aneurysm in the context of a TB cavity is called what?
Rasmussen aneurysm
42
What are the 2 main differentials for hypervascular lymph nodes in AIDs patients?
Kaposi sarcoma Castleman disease
43
AIDs patient with lung cysts, ground glass opacification and pneumothorax. What is the likely diagnosis?
PCP
44
What is the most likely diagnosis in a patient with AIDs and “flame-shaped” perihilar opacification?
Kaposi sarcoma
45
Ground glass opacification in a patient with AIDs. What is the most likely diagnosis?
PCP (could be CMV if PCP not an option and CD4 \< 100)
46
What is the most common cause of pneumonia in AIDs patients?
Strep. penumoniae
47
Pneumonia following dental procedure with osteomyelitis/chest wall invasion?
Actinomycosis
48
Bacterial pneumonia common in patients in ICU on ventilator, CF and primary ciliary dyskinesia?
Pseudomonas
49
Bacterial pneumonia which causes “currant jelly sputum”?
Klebsiella
50
An aberrant right subclavian artery will cause obliteration of what on a lateral CXR?
Retrotracheal triangle aka Raider triangle
51
What are the imaging features of proximal interruption of the pulmonary artery?
Only one pulmonary artery Absence of the PA on the opposite side of the aortic arch Volume loss of one hemithorax
52
What is proximal interruption of the pulmonary artery associated with?
Patent ductus arteriosus. Interrupted left pulmonary artery associated with tetralogy of Fallot + truncus arteriosus.
53
Thymoma is associated with what?
Myasthenia gravis Pure red cell aplasia Hypogammaglobinemia
54
Empyema necessitans, where an empyema invades into chest wall and soft tissues is classically caused by what?
TB (70%) Actinomyces is 2nd most common
55
“Shrinking lung” is associated with which condition?
SLE (most common chest manifestation is pleuritis with/without effusion)
56
Which syndrome is characterised by primary ciliary dyskinesia and situs inversus?
Kartagener syndrome
57
What are the features of primary ciliary dyskinesia?
Chronic sinusitis Conductive hearing loss Bilateral lower lobe bronchiectasis 50% have Kartagener's syndrome Impaired fertility
58
_Irregular_ focal/short segment thickening of trachea/main bronchi with calcification. What is the most likely diagnosis?
Amyloidosis
59
Circumferential thickening of the trachea with _no_ calcification C-ANCA positive. What is the most likely diagnosis?
Granulomatosis with polyangiitis | (Wegener's)
60
Diffuse thickening of the trachea with sparing the posterior membrane and no calcification. What is the most likely diagnosis?
Relapsing polychondritis
61
Cartilaginous and osseous nodules within the submucosa of the trachea and bronchial walls with sparing of the posterior membrane. What is the most likely diagnosis?
Tracheobronchopathia osteochondroplastica
62
“Headcheese” is used to describe the imaging feature of which condition?
Chronic hypersensitivity pneumonitis (Describes GGO, consolidation, air trapping and normal lungs)
63
What are the causes of cryptogenic organising pneumonia (COP)?
Idiopathic Infection Drugs (amiodarone) Collagen vascular disease Fumes
64
What are the imaging features of cryptogenic organising pneumonia?
Patchy airspace or GGO in a peripheral or peri-bronchial distribution Reverse halo/ atoll sign
65
Patients with pulmonary alveolar proteinosis are at increased risk of what infection?
Nocardia
66
What are the CT findings of chronic rejection (bronchiolitis obliterans syndrome) following lung transplant?
Air trapping Bronchiectasis Bronchial wall thickening Interlobular septal thickening
67
What is the most common opportunistic infection following lung transplant?
CMV | (2-4 months after transplant)
68
What is the imaging features of acute rejection following lung transplant?
Ground glass opacities and intralobular septal thickening. | (No ground glass → no rejection)
69
Hot quadrate sign is seen in what pathology?
SVC obstruction
70
What are the 3 main causes of pulmonary artery aneurysms?
Iatrogenic from swan ganz catheter Behcet's (also have mouth/genital ulcers) Chronic PE
71
What are the causes of fibrosing mediastinitis (soft tissue mass with calcifications infiltrating fat planes)?
Idiopathic Histoplasmosis TB Radiation Sarcoid
72
A calcified papillary muscle, seen on prenatal ultrasound as an echogenic focus in the left ventricle and usually goes away by the third trimester is associated with an increased incidence of what?
Down's syndrome
73
What is the difference between lipomatous hypertrophy of the intra-atrial septum and a lipoma?
Lipomatous hypertrophy spares the fossa ovalis creating a "dumbbell appearance" It can also be hot on PETCT because it is often made of brown fat
74
What are the branches of the left main coronary artery?
Circumflex (divides into obtuse marginals which supply lateral margin) Left anterior descending (divides into septal branches and diagonals)
75
What are the branches of the right main coronary artery?
Acute marginal AV node branch Posterior descending artery (in most people)
76
What is meant by malignant origin of the left coronary artery?
When the LCA arises from the right coronary sinus and courses between the aorta and pulmonary artery This can get compressed and lead to sudden cardiac death.
77
Reversal of flow in the left coronary artery as the pressure decreases in the pulmonary circulation, termed STEAL syndrome, is caused by what?
Anomalous left coronary artery from the pulmonary artery (ALCAPA)
78
What are the causes of coronary artery aneurysms?
Atherosclerosis (most common cause in adults) Kawasaki (most common in children) Iatrogenic
79
Velocity encoded CINE MR imaging/ velocity mapping/ phase contrast imaging is an MR technique for what?
Quantifying the velocity of flowing blood
80
What is the most common congenital heart disease?
Bicuspid aortic valve | (if not an option chose VSD)
81
What is the differential for aortic stenosis?
Atherosclerosis (degenerative) William's syndrome Rheumatic heart disease Bicuspid aortic valve
82
Williams syndrome is characterised by what features?
Craniofacial dysmorphism Short stature Intellectual disability Supravalvular aortic stenosis Pulmonary artery stenosis Renal artery stenosis Hypercalcaemia
83
What is the most common associated defect with aortic coarctation?
Bicuspid aortic valve
84
What are the associations with a bicuspid aortic valve?
Dilatation of the ascending aorta (most frequent) Congenital heart diseases (ASD/VSD, PDA, hypoplastic left heart, coarctation) Turner syndrome Cystic medial necrosis Autosomal dominant polycystic kidney disease Intracranial aneurysm
85
What are the causes of aortic regurgitation?
Aortic root dilatation (HTN/ Marfans) Aortic dissection Bicuspid aortic valve Bacterial endocarditis
86
What is the most common cause of mitral stenosis?
Rheumatic heart disease
87
What are the imaging features of mitral stenosis?
Left atrial enlargement (double density sign, splaying of the carina, posterior oesophageal displacement)
88
Isolated right upper lobe pulmonary oedema is associated with what?
Mitral regurgitation
89
What are the causes of acute mitral regurgitation?
Myocardial infarction with papillary muscle rupture (most commonly posteromedial papillary muscle) Infective endocarditis Chordae tendinae rupture in myxomatous degeneration
90
What are the causes of chronic mitral regurgitation?
Annular calcification Myxomatous degeneration Previous infective/ inflammatory illness Dilated cardiomyopathy Hypertrophic obstructive cardiomyopathy
91
What are the causes of pulmonary stenosis?
Noonan syndrome Williams syndrome Tetralogy of Fallot
92
What are the features of Alagille syndrome?
Paucity/ stenosis of the intrahepatic biliary ducts Renal anomalies (cystic kidney disease, small kidneys, nephrocalcinosis) Hypoplasia of the posterior semicircular canal Butterfly vertebrae Coarctation of the aorta Peripheral pulmonary artery stenosis
93
Peripheral pulmonary artery stenosis can be seen in what syndrome?
Alagille syndrome
94
What are the causes of pulmonary regurgitation?
Congenital valve disease repair (TOF) Pulmonary arterial hypertension
95
What are the causes of tricuspid regurgitation?
Pulmonary arterial hypertension (most common cause in adults) Ebstein anomaly (most common congenital cause) Endocarditis Carcinoid syndrome
96
What is Ebstein anomaly?
Abnormal tricuspid valve which is displaced apically into the right ventricle resulting in atrialisation of part of the ventricle above the valve.
97
What are the imaging features of Ebstein anomaly?
Severe cardiomegaly with right atrial enlargement ("box-shaped" heart) Tricuspid regurgitation
98
A right aortic arch with mirror branching is associated with what?
Tetralogy of Fallot (most common) Truncus arteriosus (2nd most common) Tricuspid atresia Transposition of the great arteries
99
What is a Kommerell diverticulum?
Bulbous origin of an aberrant subclavian artery (either left with right arch or right with left arch)
100
Cyanotic heart anomaly characterised by agenesis of the tricuspid valve and right ventricular inlet.
Tricuspid atresia
101
What are the associations with tricuspid atresia?
ASD or PFO (almost always for circulation to be complete) VSD Transposition of the great arteries Right-sided aortic arch Asplenia
102
What is the most common vascular ring?
Double aortic arch
103
What is the difference between subclavian steal syndrome and subclavian steal phenomenon?
Syndrome also has associated cerebral ischaemic symptoms
104
What are the causes of subclavian steal syndrome?
Atherosclerosis (most common) Takayasu arteritis (most common if young) Radiation Preductal coarctation of the aorta
105
Small mass attached to the inter-atrial septum by a small stalk which is iso/ hypointense on T1 weighted imaging. What is the diagnosis?
Atrial myxoma (most common location is the left atrium)
106
“Egg on a string” classically describes the CXR appearance of which congenital heart disease?
Transposition of the great arteries
107
“Snowman appearance” classically describes the CXR appearance of which congenital heart disease?
Supra-cardiac total anomalous pulmonary venous return (TAPVR)
108
“Boot-shaped” classically describes the CXR appearance of which congenital heart disease?
Tetralogy of Fallot
109
“Figure of 3” classically describes the CXR appearance of which congenital heart disease?
Coarctation of the aorta
110
“Box-shaped” classically describes the CXR appearance of which congenital heart disease?
Ebstein anomaly
111
“Scimitar sword” classically describes the CXR appearance of which congenital heart disease?
Partial anomalous pulmonary venous return (PAPVR) with pulmonary hypoplasia
112
What is truncus arteriosus?
Cyanotic congenital heart disease in which a single trunk supplies both the pulmonary and systemic circulation (cotruncal anomaly) Almost always associated with a VSD
113
Right sided aortic arch with increased pulmonary vasculature. What is the diagnosis?
Truncus arteriosus
114
Right sided aortic arch with decreased pulmonary vasculature. What is the diagnosis?
Tetralogy of Fallot
115
What is Tetralogy of Fallot?
Right ventricular outflow obstruction Ventricular septal defect (VSD) Right ventricular hypertrophy Overriding aorta
116
Tetralogy of Fallot is associated with which extra-cardiovascular conditions?
Congenital lobar emphysema DiGeorge syndrome Fetal rubella syndrome Prune belly syndrome Tracheo-oesophageal fistula VACTERL association
117
In which congenital heart diseases will the child be cyanotic?
Tetralogy of Fallot Total anomalous pulmonary venous return (TAPVR) Transposition of the great arteries Truncus arteriosus Tricuspid atresia
118
What is transposition of the great arteries?
The aorta arises from the right ventricle and the pulmonary trunk arises from the left ventricle Presents in first 24 hours of life with cyanosis Survival requires ASD, VSD or PDA
119
What is L-type transposition of the great arteries?
“Lucky type" Congenitally corrected TGA where the right atrium connects with the left ventricle and the left atrium connects with the right ventricle A PDA is therefore not required
120
Following a LeCompte Maneuver, a patient has their pulmonary arteries draped over the aorta. What was this procedure carried out for?
Corrected D-transposition of the great arteries
121
What is the most common VSD?
Membranous (just below the aortic valve)
122
What is a patent ductus arteriosus?
Persistent patency of the ductus arteriosus, a normal connection of the fetal circulation between the aorta and the pulmonary arterial system.
123
What is the most common type of ASD?
Secundum
124
Which syndrome would you find an ASD and upper limb anomalies?
Holt-Oram syndrome
125
Secundum ASD and atrioventricular septal defects (AKA endocardial cushion defect) is associated with which syndrome?
Down's syndrome
126
A sinus venosus ASD is associated with what congenital heart disease?
Partial anomalous pulmonary venous return
127
Unroofed coronary sinus is strongly associated with which normal variant?
Persistent left SVC
128
What is partial anomalous pulmonary venous return?
Where 1 (or more) pulmonary veins drain into the right heart (most common: right upper pulmonary vein connects to RA/ SVC. Often associated with a sinus venosus ASD)
129
What is total anomalous pulmonary venous return?
Cyanotic heart disease where all of the pulmonary veins drain into the right side of the heart Requires a large PFO or ASD (less commonly) for survival
130
Right sided PAPVR is associated with what?
Sinus venosus type ASD
131
Right sided PAPVR with pulmonary hypoplasia. What is the diagnosis?
Scimitar syndrome
132
There are 3 types of TAPVR. Which is the most common?
Type 1: supracardiac (gives snowman appearance)
133
There are 3 types of TAPVR. Which type gives full on pulmonary oedema appearance in the newborn?
Type 3: infracardiac (veins drain below the diaphragm)
134
Of the patients with asplenia who also have congenital heart disease (approx 50%), how many have TAPVR?
100% 85% also have endocardial cushion defect (AV canal/ atrioventricular septal defect)
135
What is the most common complication following surgery for tetralogy of Fallot?
Pulmonary regurgitation
136
Which ribs are involved in rib notching, secondary to aortic coarctation?
4-8th ribs (does NOT involve 1st and 2nd as those are supplied by the costocervical trunk)
137
What pathology gives you a tri-atrium heart?
Cor triatriatum sinistrum (abnormal pulmonary vein draining into the left atrium with an unnecessary fibromuscular membrane that causes a sub-division of the left atrium)
138
What is a stunned myocardium?
Dysfunction of the myocardium which persists after restoration of blood flow following an acute injury (MI or reperfusion injury)
139
What are the imaging features of a stunned myocardium?
Abnormal wall motion Normal perfusion on Thallium and Sestamibi
140
What is a hibernating myocardium?
Chronic process resulting from severe coronary arterial disease causing chronic hypoperfusion There will be areas of decreased contractility and perfusion even when resting Reversible with revascularisation
141
What are the imaging features of hibernating myocardium?
Areas of decreased perfusion and contractibility Increased tracer uptake on PETCT Redistribution of Thallium
142
How is delayed cardiac imaging performed to look for infarction?
Inversion recovery technique to null normal myocardium followed by gradient echo. Bright on T1 = dead.
143
How can you differentiate acute from chronic MI?
Acute: delayed enhancement, normal thickness myocardium, increased T2 from oedema Chronic: delayed enhancement, thinned myocardium, T2 dark (scar)
144
Microvascular obstruction, where islands of dark tissue are seen in amongst late Gd enhancement (i.e contrast is unable to get to these regions) is a poor prognostic finding seen in which kind of MI?
Acute It's NOT seen in chronic infarct
145
Ventricular aneurysms can occur secondary to MI. What are the features of a TRUE aneurysm?
Mouth is wider than body Myocardium is intact Antero-lateral wall
146
Ventricular aneurysms can occur secondary to MI. What are the features of a FALSE aneurysm?
Mouth is narrow compared to body Myocardium is NOT intact Posterior-lateral wall *higher risk of rupture*
147
Dressler syndrome is seen how long after a myocardial infarction?
4-6 weeks
148
What is the symptoms of Dressler syndrome?
Pleuritic chest pain, fever, malaise Pericardial effusion Leucocytosis/ raised inflammatory markers
149
What is the differential for restrictive cardiomyopathy?
Amyloid (most common) Endocardial fibroelastosis Haemochromatosis
150
What are the imaging features of cardiac amyloidosis?
Intra-atrial septal thickening and biatrial enlargement Concentric thickening of the left ventricle Subendocardial delayed myocardial hyperenhancement Granular echogenic myocardium Long T1 required. Buzzword: “*difficulty suppressing myocardium*”
151
What are the imaging features of cardiac sarcoidosis?
Nodular or patchy increased signal on T2 and enhanced images, often involving the septum (esp basal) and LV wall Right ventricle and papillaries rarely involved Focal wall thickening from oedema
152
What is the most common primary malignancy of the heart in adults?
Angiosarcoma
153
What is the imaging features of a cardiac angiosarcoma?
“Sun-ray appearance” Commonly right atrium involving the pericardium Bulky and heterogenous
154
How would you differentiate an atrial myxoma from a thrombus?
Myxoma will enhance Myxoma will be attached to the inter-atrial septum
155
Atrial myxoma is associated with what syndrome?
Carney complex
156
What is the most common fetal cardiac tumour and what are the imaging appearances?
Rhabdomyoma Typically arise within the ventricular myocardium (left more common) Isointense to myocardium on T1, mildly hyperintense on T2 and no enhancement
157
What are the imaging features of a cardiac fibroma (2nd most common cardiac tumour in childhood)?
Most common location is left ventricle and interventricular septum Dark on T1/T2 imaging Enhance avidly
158
What is the definition of adenocarcinoma in situ in the lung?
\< 3cm No features of necrosis or invasion
159
What is the definition of minimally invasive adenocarcinoma of the lung?
\< 3cm \< 5mm of stromal invasion
160
What is the first branch of the SMA?
Inferior pancreaticoduodenal artery
161
What arteries make up the arc of Riolan?
Left colic (from IMA) to middle colic (from SMA)
162
Which branches of the internal iliac arteries are from the posterior divisions?
Iliolumbar Lateral sacral Superior gluteal
163
What is the relationship of the subclavian vessels with the anterior scalene muscle?
The subclavian veins runs anterior to the muscle, the artery runs posterior
164
When does the subclavian artery become the axillary artery?
At the 1st rib
165
When does the axillary artery become the brachial artery?
At the lower border of teres major
166
When does the external iliac artery become the common femoral artery?
Once it gives off the inferior epigastric artery at the inguinal ligament
167
Most gastric varices are formed by which vein?
Left gastric vein (coronary vein)
168
Isolated gastric varices are caused by what?
Splenic vein thrombosis
169
Where do gastric varices drain?
Into the inferior phrenic, then into the left renal vein (forming a gastro-renal shunt)
170
Enlarged left renal vein with enlargement of the IVC at the level of the left renal vein can be caused by what?
Splenorenal shunt caused by portal hypertension Associated with hepatic encephalopathy NOT associated with GI bleeding
171
What is the most common congenital heart disease associated with a left IVC?
ASD
172
Azygous continuation of the IVC is associated with what splenic abnormality?
Polysplenia
173
What are the causes of aortic dissection?
Hypertension (most common) Marfans Turners (aortic valve defects) Infection Pregnancy Cocaine use
174
How do you identify the true lumen in aortic dissection?
Continuous with the undissected portion of the aorta Smaller cross sectional area Surrounded by calcification (if present) Usually contains the origin of the coeliac trunk, SMA and right renal artery
175
How do you identify the false lumen in aortic dissection?
“Cob-web sign”: linear areas of low attenuation Larger cross-sectional area Beak sign Usually contains the origin of the left renal artery Surrounds the lumen in type A dissection
176
What are the causes of ascending aortic calcification?
Takayasu arteritis Syphilis
177
Cystic medial necrosis is associated with which syndrome?
Marfan's syndrome
178
Describe a type 1 endoleak?
Leak at the top or the bottom of the graft
179
Describe a type 2 endoleak?
Filling of the aneurysm sac via feeder arteries (most likely IMA or a lumbar artery)
180
Describe a type 3 endoleak?
Defect/ fracture in the graft
181
Describe a type 4 endoleak?
Porosity of the graft (doesn't usually happen with modern grafts)
182
Describe a type 5 endoleak?
Endotension
183
What is the most common endoleak?
Type 2
184
What are the imaging findings of impending aortic aneurysm rupture?
Peri-aortic stranding Rapid enlargement (\>10mm per year) Draped aorta sign Focal discontinuity in circumferential wall calcification Hyperdense crescent sign
185
What are the vascular features of Marfan's?
Dilatation of the aortic root Aortic valve insufficiency/ severe aortic regurgitation Aortic aneurysm/ dissection Pulmonary artery dilatation
186
Which part of the bowel is most commonly involved in aorto-enteric fistula?
3rd and 4th parts of the duodenum
187
How can you differentiate between aorto-enteric fistula and perigraft infection?
You can only differentiate if you see contrast from the aorta go into the bowel lumen Both have perigraft gas, perigraft fluid and oedema and both lose the fat plains between the bowel and the aorta
188
What is Leriche syndrome?
Complete occlusion of the aorta, distal to the renal arteries (often secondary to bad atherosclerosis)
189
What is the triad associated with Leriche syndrome?
Buttock claudication Absent/ decreased femoral pulses Impotence
190
Young adult presents with hypertension, claudication and renal failure. CT shows progressive narrowing of the abdominal aorta and the major branches. What is the diagnosis?
Mid-aortic syndrome (thought to be secondary to intrauterine insult)
191
Elongation with narrowing and kinking of the aorta but no pressure gradient, collateral formation or rib notching. What is the diagnosis?
Pseudocoarctation (area of dilatation may occur distal to the area of narrowing and may be progressive so should be followed up)
192
What is the most common cause of thoracic outlet syndrome?
Compression by the anterior scalene muscle
193
What are the causes of TRUE splenic aneurysms?
Pregnancy Hypertension Portal hypertension Cirrhosis Liver transplant
194
What is the most common location involved in chronic mesenteric ischaemia?
Splenic flexure | (watershed area of the SMA and IMA)
195
What are the imaging features of colonic angiodysplasia?
Right sided Cluster of small arteries along the antimesenteric border of the colon Early opacification of dilated draining veins that persist late into the venous phase
196
Aortic stenosis and colonic angiodysplasia is referred to by which syndrome?
Heyde syndrome
197
Which arteries are most commonly involved in fibromuscular dysplasia?
Renal arteries (most common) Carotid arteries Iliac arteries
198
“String of beads” description of arteries is seen in which condition?
Fibromuscular dysplasia
199
What is May-Thurner syndrome?
Compression of the left common iliac vein by the right common iliac artery resulting in DVT
200
Young man with normal lower limb pulses which decrease with plantar flexion or dorsiflexion of the foot. Imaging shows medial deviation of the popliteal artery. Diagnosis?
Popliteal entrapment
201
Syndrome with a triad of port wine naevi, bony/soft tissue hypertrophy and venous malformation, often associated with a persistent sciatic vein. The marginal vein of Servelle (in lateral calf) is said to be pathognomonic.
Klippel-Trenaunay syndrome
202
What is a normal ankle to brachial index (ABI)?
1.0
203
At which ABI will patients experience rest pain?
\< 0.3
204
What is the most likely cause of re-stenosis 3-12 months after angioplasty?
Intimal hyperplasia
205
Takayasu tends to affect which patients?
Young Asian girls, typically aged 15-30
206
Polyarteritis nodosa (PAN) commonly affects which systems?
Renal (microaneurysms) Cardiac GI
207
Polyarteritis nodosa is associated with what?
Hepatitis B More common in men
208
What is the most common vasculitis in children?
Henoch-Schonlein purpura (HSP)
209
Which vasculitis is strongly associated with smokers and the development of corkscrew collateral vessels. Buzzword = auto-amputation
Buergers
210
HSP is associated with what?
Intussusception Massive scrotal oedema
211
What are the contraindications to beta-blockers?
2nd/3rd degree heart block severe asthma acute chest pain recent snorting of cocaine
212
What are the contraindications to nitroglycerine?
hypotension (SBP \<100) severe aortic stenosis HOCM phosphodiesterase
213
What are the branches of the external carotid arteries?
Some Anatomists Like Freaking Out Poor Medical Students Superior thyroid Ascending pharyngeal Lingual Facial Occipital Posterior auricular Maxillary Superficial temporal
214
Cardiac MRI finds circumferential endocardial fibrosis and biventricular thrombi. What is the most likely diagnosis?
Loeffler endocarditis Can be distinguished from amyloidosis by the adherent ventricular thrombi. Patients will also have peripheral blood eosinophilia
215
What are the imaging features of lymphocytic interstitial pneumonitis?
Mid to lower zone predominance Thickening of bronchovascular bundles and interstitial thickening Scattered thin walled cysts
216
Mosaic perfusion with no air trapping. What is the most likely diagnosis?
Pulmonary emboli
217
What is the most common CT chest finding in patients with history of acute respiratory distress syndrome?
Reticular changes in the anterior/ventral non-dependent lung
218
What are the radiographic findings of acute rejection following lung transplant?
Ground glass opacity Heterogeneous peri-hilar opacification New enlarging pleural effusion with septal thickening No signs of left ventricular failure
219
The bronchial tree receives blood from one right and two left bronchial arteries. From which vessel does the single right artery usually arise?
Third posterior right intercostal artery
220
What are the imaging features of pulmonary hamartomas?
Peripheral Popcorn calcification Fat in 50%
221
What are the imaging features of pulmonary carcinoid?
Tend to be more central and endobronchial in location Calcification Rarely cavitate No fat Prominent enhancement following contrast
222
What is the most common pulmonary finding on chest radiograph in rheumatoid arthritis?
Pleural effusion
223
Which lung segments are separated by the superior accessory fissure?
Apical segment of the lower lobes from the other lower lobe segments
224
Which lymphoma is usually almost entirely confined to the lymph nodes?
Hodgkins lymphoma
225
Pulmonary involvement in Hodgkins lymphoma indicates which stage of disease?
Stage IV
226
What is the dose for a CT pulmonary angiogram relative to a V/Q scan?
CT pulmonary angiogram has a higher total body dose but a lower uterine dose
227
What are the imaging features of amiodarone lung disease?
Alveolar and interstitial infiltrates and high density areas of consolidation (iodine)
228
What is hypertrophic obstructive cardiomyopathy?
Diffuse or segmental left ventricular hypertrophy with a non-dilated and hyperdynamic chamber in the absence of another condition to explain the hypertrophy
229
What are the imaging appearances of hypertrophic obstructive cardiomyopathy?
Asymmetric involvement of the interventricular septum is most common (60-70%) Hypertrophy of the muscle to \> 15mm in diastole “Spadelike” configuration of LV cavity at end diastole
230
What are the features of Kawasaki disease?
Fever and maculopapular rash Cervical lymphadenopathy Coronary artery aneurysms Myocarditis/ pericarditis/ pericardial effusions/ valvular disease
231
Where do cardiac fibroelastomas commonly arise and what is the key feature on imaging?
Cardiac valves (80% are aortic or mitral) Intense enhancement on delayed imaging (this is how they can be differentiated from a vegetation)
232
Dissection of the cervical portion of the ICA can result in which symptoms?
Partial Horners syndrome (miosis and ptosis) MCA territory stroke
233
Aneurysm with the origin at the “dural ring” is found where?
Ophthalmic (supraclinoid) segment of the internal carotid artery
234
Where are the most common sites of aneurysm formation in the posterior intracranial circulation?
Basilar (most common) PICA
235
“Caput medusa” and “large tree with multiple small branches” are terms used to describe what?
Developmental venous anomaly (associated with cavernous malformations)
236
What are the imaging features of intracranial cavernous malformations?
“Popcorn- like” with peripheral rim of haemosiderin without intervening normal brain tissue
237
The “crescent sign” of dissection is seen on which MRI sequence?
T1 (will be bright)