Practice viva Flashcards

1
Q

Pulmonary hypertension, plain film

A

Elevated apex - RVH
Enlarged right atrium
Prominent pulmonary outflow tract, enlarged pulmonary arteries
Pruning of peripheral pulmonary vessels

Mural calcification of pulmonary vessels highly specific - seen in Eisenmengers

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2
Q

Pulmonary HTN 2008 world sympsosium

A

PA pressure >25, wedge pressure >15

1 - idiopathic, drug toxin induced, connective tissue disease
2 - left sided heart disease
3 - lung disease or hypoxia - COPD, interstitial lung disease
4 - thromboembolism
5 - multifactorial

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3
Q

Mediastinal mass localisation

A

Mediastinal masses create obtuse angles with lung, and disrupt mediastinal lines

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4
Q

Anterior mediastinal mass

A

Obliterated retrosternal clear space
Loss of sharp ascending aorta or anterior junctional line (lower of the two lines, doesn’t go above 1st rib / clavicle)
Hilum overlay (most will be anterior)
Loss of cardiophrenic angle

Lymphoma most common child (actually thymic hyperplasia 1), thymic adult

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5
Q

Middle mediastinal mass

A

To 1cm posterior to anterior vertebral line
AP window, paratracheal stripes
Azygooesophageal recess displacement (Right - new intervace, looks like a paravertebral line) (Can be displaced by posterior mass)
Left pseudoparavertebral line
Mass on posterior trachea on lateral
Doughnut sign - mass surrounds bronchus on lateral

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6
Q

Lateral chest x-ray (add stuff from the MCQ file)

A

.

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7
Q

Cervicothoracic sign

A

Superior border of mass descernible, above the clavicels

Must be in Apical upper lobe, pleural, or posterior medastinum

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8
Q

Foregut duplication cyst

A

Generic term
Encompasses neurenteric cysts and bronchogenic cysts., oephageal
Bronchogenic tend to be middle mediastinum, neurenteric posterior.

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9
Q

Paeds mediastinal masses

A

Lymphoma most common anterior
Duplication cyst most common middle
Neurogenic tumour most common posterior

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10
Q

ECMO

A

Venoarterial or venovenous
Venoarterial - out via right atrium (via femoral or IJV), in via femoral, subclavian artery line, aorta.
Venovenous - In and out via central venous lines. Can have double lumen catheter.
Anticoagulated (consider if need to put chest drain)

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11
Q

Mitral stenosis

A

Often secondary to rheumatic fever
Left atrial enlargement - splayed carina, elevation left main bronchus, convex left atrial appendage, double right heart border,
Upper lobe venous engorgement from venous hypertension

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12
Q

Other valvular diseases?

A

.

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13
Q

Chest wall soft tissues

A

Alway evaluate for mastectomy

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14
Q

Secondary findings

A

E.g. right sided arch, but also lymphoma

Or additional aberrant subclavian

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15
Q

Primary TB

A

Patchy or lobar consolidation, any lobe, preference for middle and lower lobes
Lymphadenopathy (especially in children - 90%, only 10-30% adults. Low density with rim enhancement)
May be miliary (immunocompromised more)
Pleural effusions (30-40% adults, 10% children)
May resolve without any radiological abnormality, or Ghon focus scar may remain (calcified granuloma)
Symptoms only in 5%
Cavitation uncommon
May have massive haemoptysis from erosion into a bronchial artery

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16
Q

Secondary TB

A
Upper zone predominant
Far more likely to cavitate
Lymphadenopathy less common
Effusion less common
Usually patchy
Can have lobar consolidation, miliary, tuberculoma
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17
Q

Massive haemoptysis

A
Cancer
Bronchiectasis, bronchitis
TB
Aspergilloma
Pneumococcal
Contusion
PE
Other

Bronchiectasis is most common cause of bronchial artery hypertrophy leading to massive haemoptysis

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18
Q

Left atrium, congenital

A

Enlarged in VSD, PDA. Normal size in ASD

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19
Q

Left atrial enlargement

A

Congenital (VSD, PDA)

Or acquired - mitral valve disease, most commonly Rheumatic

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20
Q

Tetralogy of fallot

A

VSD
Overarching aorta
Pulmonary stenosis
RVH

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21
Q

Dilated ascending aorta

A
Aneurysm
HTN
Dissection
Coarctation
Valvular disease including bicuspid valve
Congenital heart disease
Connective tissue disorders.
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22
Q

Bicuspid aortic valve

A
Major cause of aortic valve disease in young adults
2% incidence, more common in males
Dilated ascending aorta
70% of coarctations have bicuspid valve
10% of Turners have it
Associated with ADPKD
Associated with berry aneurysms
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23
Q

Pacemaker

A

Single chamber
Dual chamber
Biventricular (additional lead through coronary sinus to left ventricular vein)

Coronary sinus drains to RA, drains cardiac veins, courses along posterior LA.
Unroofed coronary sinus has opening to LA also, a rare ASD
Hiccups?

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24
Q

Ribbon ribs

A

Thinned ribs
Commonly due to neurofibromas in NF1
Also seen in OI, Edwards (18), Gorham disease (progressive massive osteolysis)

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25
Q

Left to right shunt

A

ASD, VSD, PDA, AVSD

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26
Q

Sarcoid, biochemical markersm, imaging stage

A

ACE - 40% false negative, 10% false positive
30-50% hypercalcuric, 10-20% hypercalcaemic
May be stage 1-3 at presentation, unlikely 4 (fibrosis)

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27
Q

Common cavitating lesions

A

Malignancy most common
Then infection
Cancer, autoimmune, vascular, infection, trauma, young
Sarcoid can cavitatae

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28
Q

Transposition

A

L - congenitally corrected
D - egg-on-a-string - narrowed superior mediastinum due to stress thymic atrophy and pulmonary hyperexpansion, parallel great vessels, globular heart from LA enlargement and convex RA
L - AV discordance and VA discordance
Plain film appearance?

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29
Q

Scleroderma

A

Dilated oesopagus
Soft tissue calcification - subcutaneous and periarticular

Acroosteolysis
Finger contractures
Atrophic finger tips
Resorption

UIP, NSIP, PAH
Egg-shell calcification of mediastinal nodes (seen in other conditions e.g. silicosis (more pathognomonic of this), treated lymphoma rarely sarcoid)

30
Q

TIP

A

Be wary of recommending CT on chest viva. Get most out of the plain film

31
Q

Cystic lung disease

A

LIP (Sjogrens, women), LAM, LCH (smokers)
LIP lower zone (and ground glass), LCH upper (nodules which cavitate), LAM uniform (prone to chylothoraces and pneumothoraces)

UIP, Cystic bronchiectasis, pneumocystis, pulmonary lac

Burt-Hogg-Dube - Lower zone lung cysts, chromophobe RCC and oncocytomas, cutaneous manifestations, chromosome 17, AD, rare

32
Q

Pneumomediastinum

A
Asthma
Barotrauma
Interstitial lung disease
Infection
Booerhaves
Oesophageal cancer
33
Q

Supine pneumothorax

A

Deep sulcus

34
Q

Cannonball mets

A

RCC, choriocarcinoma

Less commonly, prostate, synovial, endometrial. bladder TCC

35
Q

Chest wall mass

A

Soft tissue, benign, malignant
Ribs, benign, malignant

ST B - haemangioma, lymphangioma, lipoma, nerve sheath
ST M - rhabomyosarc, Askin Ewings sarc, malignant fibrous histiocytoma (/PUS), neuroblastoma, malignant peripheral nerve sheath tumour
Ribs B - Fibrous dysplasia, ABC, GCT
Ribs M - myeloma, mets, osteosarcoma, chondrosarcoma

36
Q

TNM staging of lung cancer

A

.8th edition staging 2016
T1 <3, 2 2-5 or main bronchial involvement or atelectatic, 3 5-7 or tumour nodule same lobe, 4 >7 or tumour nodule different lobe or invasive
N1 ipsilateral hilar, N2 ispilateral mediastinal or subcarinal, N3, contraleteral mediastinal or hilar, or supraclavicular
M1a - pleural or pericardial, b single extrathoracic, c multiple extrathoracic

Once N3 or T3/4 N2, can’t operate, stage 3b

37
Q

Posterior medastinal mass

A

Neurogenic tumour - benign and malignant (most common. Includes neurofibroma, schwannoma, MPNST, neuroblastoma, ganglioneuroblastoma, ganglioneuroma - ganglioneuroma most common, with both the ganglios in older patients than neuroblastoma)
Neurenteric duplication cyst
Paravertebral mass - include abscess, haematoma, mets
Descending thoracic aneurysm
Lymphadenopathy / extramedullary haematopoiesis
Oesophageal neoplasm
Also pancreatic pseudocyst, dermoid, sarcoid

38
Q

Double aortic arch

A

Narrowed trachea
Most common symptomatic aortic arch variant
50-60% of vascular rings

39
Q

Thoracic nodal stations

A
1 - supraclavicular
2-4 - superior medastinal
5-6 - aortic
7-9 - Inferior mediastinal
10-14 - N1 nodes, hilar, then through lungs

2 upper paratracheal
3 prevascular and retrotracheal
4 lower paratracheal

5 AP window
6 para-aortic

7 subcarinal
8 paraoesophageal (below carina)
9 pulmonary ligament

10 hilar
11 interlobar
12 lobar
13 segmental
14 subsegmental
40
Q

Dense bones and no splenic flexure visible

A

Myelofibrosis with splenomegaly

41
Q

Hampton hump

A

Dome-shapled pleural based opacification from embolism and infarction
The apex of the wedge may be spared due to collateral supply causing the rounding.
If infarcts, linear scar. Otherwise melting sign.

42
Q

Diffuse alveolar haemorrhage

A

Vasculitis (Wegeners, Churg-strauss, Goodpastures), SLE, coagulation disorder, PE, mitral stenosis and regurg, diffuse alveolar damage

43
Q

PCP

A
CD4 <200
Lavage to confirm diagnosis
Perihilar distribution
Pneumatoceles and subpleural blebs
Effusions rare
Adenopathy uncommon (10%)
44
Q

PCP

A
CD4 <200
Lavage to confirm diagnosis
Perihilar distribution
Pneumatoceles and subpleural blebs
Effusions rare
Adenopathy uncommon (10%)

Atypical findings more common in those receiving aerosolised prophylaxis - upper lobe predominant, adenopathy, effusions

45
Q

Malplaced PICC line

A

Going into neck

46
Q

Malplaced intercostal drain

A

Straight course, in a fissure

47
Q

Miliary metastases

A

Breast, ovarian, thyroid, renal, melanoma, pancreatic, trophoblasic

48
Q

Metastatic calcification

A

Centrilobular ground glass nodules, may appear calcified
Upper zone predominant
Renal failure most common
But also primary HPT, sarcoid, osteolysis e.g. mets, vit D intoxication

49
Q

Right sided aortic arch

A

Mirror image branching associated with cyanotic heart disease - TOF, truncus, tricuspid, transposition
Aberrant left no association

50
Q

Pericardial effusion, mm

A

Must be at least 3mm on CT

51
Q

Bronchial carcinoid

A
Bronchial obstruction, wheeze
Carcinoid syndrome rare (diarrhoea, flushing, RHF, bronchospasm, pain, from excess serotonin)
May produce Cushings
Association with MEN1
Marked homogeneous contrast enhancement
Endobronchial
Can have peripheral calc but not common
52
Q

Cystic adventitial disease

A

Young to middle age without evidence of vasculitis or atherosclerosis
Male predominant
Peripheral arteries
Striking prediliction for popliteal region
See cysts in the wall, which may displace the artery
Main differential in popliteal region is popliteal artery entrapment syndrome (medial head of gastroc, or popliteus or fibrous band)

(not same as cystic medial necrosis or degeneration, seen in aorta in Marfans)

53
Q

Upper lobe predominant

A

Beryllosis, radiation, EAA (HSP), ank spond, sarcoid, TB (secondary), histiocytosis X (metastatic calc and PCP in patients receiving prophylaxis)

54
Q

Hypersensitivity pneumonitis

A

Upper lobe predominant
Bird fanciers, hot-tub
Ground glass, centrilobular nodules, air trapping,

Small airways inflammation, interstitial lymphocytic infiltrates, granuloma formation
Fibrosis in latter stages

55
Q

CAVITY

A

Cancer (SCC), autoimmune (Wegeners, RA), vascular (PE), infection (abscess, TB), trauma, young (CPAM, sequestration, cyst)

56
Q

VOTE SSSX

A

.

57
Q

Pulmonary hamartoma

A

6% of solitary pulmonary nodules
Fat pathognomonic
Popcorn calc

Other benign option is chondroma, but has ossified segments, form part of Carneys triad

58
Q

Carneys triad

A

Pulmonary chondroma, GIST, spinal paraganglioma

59
Q

Grid cutoff

A

Can stimulate assymetric lucency / opacity

60
Q

NF1 MSK manifestations

A
Rib notching
Ribbon ribs
Vertebral body scalloping
Limb bowing
Limb pseudoarthroses - tibial, ulnar
Scoliosis
Multiple non-ossifying fibromas
61
Q

Chronic airspace opacity

A

Organising pneumonia (peripheral), chronic eosinophilic pneumonia (upper lobe predominant usually)
Atypical infection - TB, fungal
Neoplasia esp adenocarcinoma, also consider lymphoma

62
Q

Other lung patterns e.g. crazy paving

A

.

63
Q

Don’t forget to look at neck

A

Don’t forget

64
Q

Perilymphatic nodules

A

Sarcoid, lymphangitis, silicosis

Coal pneumoconiosis, amyloidosis, LIP

65
Q

Centrilobular nodules

A
Infection
Neoplasia with airway spread
HSP
RB-ILD (becomes DIP) (lower zone predominant)
Vasculitides e.g. Churg-Strauss
66
Q

Random nodules

A

Haematogenous mets, septic emboli

67
Q

Lateral radiograph

A

.

68
Q

Plombage

A

Extrapleural pneumonolysis
Historical treatment of upper lobe cavitatory TB
Surgical cavity created under upper ribs, filled with inert material e.g. ping pong balls, parrafin wax, gauze, acrylic / lucite balls

69
Q

Oleothorax

A

.

70
Q

Thoracoplasty

A

.

71
Q

Thoracic lymph node levels

A
10 hilar
11-14 Interlobar through subsegmental
7 subcarinal
1-6 higher than carina
8-9 lower than carina