Respiratory Flashcards

(72 cards)

1
Q

non cardiac APO

A
HARD MONTH
Head injury
ARDS
Radiation, Renal failure
Drugs - C+ media, narcotics,  heroin
MI
O2 therapy
Near drowning 
Transfusion reaction 
HP
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2
Q

Batwing

A

Pulmonary oedema
Bronchopn
PCP
Viral pn

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3
Q

Reverse batwing

A
OP
Bronchoalv  carcinoma
Sarcoidosis
EG pn.
vasculitis
contusion
pulm haemorrhage
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4
Q

Anterior mediastinal mass fx

A
Hilum  overlay 
Obliterates l & r heart border
Paravertabral/Para tracheal stripe thick
Blunt margins above clavicle
Retrosternal clear space preserved on lateral
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5
Q

Anterior mediastinal mass ddx

A
5Ts
thyroid
teratoma
terrible lymphoma
thymoma
thoracic aorta
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6
Q

Middle mediastinal mass fx

A
lt and rt paratracheal stripe >5mm
loss of Aortopylm window
loss of hilarious strictures visible
loss SVC
lateral doughnut sign
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7
Q

middle mediastinal mass ddx

A
LN
bronchial ca
vascular aneurysm
bronchitis cyst
tracheal mass
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8
Q

posterior mediastinal mass fx

A

widened Paravertabral lines
cervicothoracic sign
azygo-oesophageal line disrupted
hilum and cardiac borders visible

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9
Q

Posterior mediastinal mass ddx

A

along VBS - Mets, myeloma, extramedullary haematopoiesis, ganglioneuroma
anterior upper - oesophageal, aorta, thyroid
anterior lower - hiatus hernia, bochdalek hernia

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10
Q

if PE go to limb aa

A

must have PFO. need to do echo to assess heart and urgent embolectomy or thrombolysis
when have PE always suggest assess for DVT

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11
Q

thallium vs gallium

A

thallium. Kaposi sarcoma and lymphoma both positive

gallium. lymphoma positive, Kaposi negative

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12
Q

upper lobe fibrosis

A
CASSET P
CF
Ank spon
Sarcoidosis
Silicosis
EG
Tb
PCP
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13
Q

halo

A

infective, neoplasm, haemorrhage, other

infective. atypical ( fungus, angio invasive, cryptococcus coccidicoyoycosis,),,mycobacteria, septic embolism, viral (HSV, cmv)
neoplasm. lymphoma, adenocarcinoma, Kaposi, scc
haem. trauma, Wegeners
other. EG, op,

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14
Q

reverse halo

A
fungal pn
op
Tb
infarct
Wegeners
radiation necrosis 
alveolar sarcoid
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15
Q

cavitation

A
CAVITY
CA.  SCC, mets
autoimmune - rheumatology nodule, PMF
Vascular. Wegeners 40s, good pastures 20s. check kidneys. septic or bland embolism
Infection. staph, Tb,  klebsiella, staph
Trauma. pneumatocele, haematoma
Youth. CCAM,  sequestration
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16
Q

non resolving consolidation

A
wrong abx
immunocompromised
bronchial obstruction
recurrent aspiration
underlying pathology. abscess, bronchiectesis, sequestration, mass
organising pneumonia
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17
Q

pulmonary calcification

A

single focus:
granuloma. previous mycoplasma infection
hamartoma. fat
neoplasm. carcinoid, GI (central or popcorn), osteosarcoma ( solid)
rxt
old infarct or injury

multiple foci:
healed miliary Tb, fungal or VCV
silicosis
post rx lymphoma
alveolar microlithiasis (sand lung)
interstitial:
chronic bronchitis
ARDS
asbestosis
busulphan long term use
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18
Q

eggshell ca+

A
Tb
sarcoid
silicosis
pneumoconiosis
lymphoma. post rx
ddx: pulm aa, aortic, ant mediastinal mass (thymoma, teratoma)
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19
Q

unilateral hyperlucent hemithorax

A
Swyer James.  post viral or mycoplasma as child
Pulm agenesis with hypertrophy other lung
Pneumonectomy
Ptx
Obstruction with air trapping
Embolism
Mucous plug
Mastectomy 
Poland sx
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20
Q

bilateral hyperlucency

A

Normal lung volume:
oligaemia 2ndry to congenital heart abno. rt to lt shunt
bilateral PE
pulm htn

Increased lung vol:
emphysema
asthma
bronchiolitis. kids <1yo

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21
Q

unilateral opacity hemithorax

A
mediastinum centre:
airspace opacity. infection, oedema, haem, tumor
pleural effusion
chest wall mass/lipoma
rotation
mediastinum towards opacity:
vol loss. obst with atelectesis
Pneumonectomy
pulm agenesis/hypoplasia
mesothelioma
mediastinum away from opacity:
mass effect.  
mesothelioma
pleural effusion, hemithorax,  chylothorax
red hepatisation
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22
Q

bronchial obst

A

within lumen. inh Fb, mucous plug, ett, aspergilosis, bronchiolithiasis
within wall. carcinoid, bronchogenic ca, sarcoid, bronchial atresia, # bronchus
external. mediastinal mass. LN, primary or 2ndry malig, aortic aneurysm, LA enl, anomalous lt pulm aa arising rt pulm aa (rt main bronchus obst)

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23
Q

bronchiectesis

A

UL. CF, rxt, Tb, ABPA, endoluminal mass
ML. lady wyndimere non Tb mycoplasma. Mac
LL. ciliary dyskinesias, kartagners, asthma, chronic aspiration, ctd, viral infection as child, CCAM, ABPA, Williams Campbell (no cartilage in walls)

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24
Q

CF
bugs
abdo manifestations
chest manifestations

A

mycoplasma, pseudo Minas, staph aureus

abdo: me plug, rectal prolapse, cirrhosis, panc atrophy or ca+, GORD
chest: recurrent infections, ABPA, bronchiectesis UL bilateral, Pulm aa htn with bronchial aa dilatation

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25
airspace opacity
acute or chronic Acute: fluid. cardio and non cardio haem. Wegeners, good pastures, contusion, Pulm heamosiderosis, anti GBM infection. PCP, Tb, VCV, viral pn, bronchopn infarct ``` Chronic. sarcoid EG OP lymphangitis ca Malignancy. adenoca, lymphoma lipid pn sequestration ```
26
pulmonary cysts
LCH. nodules>cavitate>bizarre cysts. smoker. LAM. even distribution. female childbearing age. check kidneys for AML and uterus for leiomyoma LIP. smooth and scattered. GGO and nodules. bronchovascular thickening. immunocompromised or CTDs Birt hogg dube. AD. pulm cysts basal and large +/- multiseptated, bilateral renal RCC/Oncocytoma and cutaneous angiofibromas acquired. PCP, cystic bronchiectesis, honeycombing, end stage sarcoid, pneumatocele, cryptococcus, staph a, hydatiform congenital. CCAM, congen lobar emphysema, pie, bpd
27
nodules mx
benign ca (solid, popcorn, lamellar, central, target), fat = leave alone 4-8mm flies cheer >8mm bx, PET
28
SPN
``` granuloma primary neoplasm met hamartoma carcinoid infection. pneumonia (round in kids, pneumococcal), hydatid, round atelectesis, OP autoimmune. RA, Wegeners, sarcoid vascular. AVM (multiple HTT), haematoma congenital. sequestration, bronchogenic cyst, intrapulm LN ```
29
mets to lung
breast sarcoma RCC seminoma
30
cannonball mets
rcc chorioca prostate
31
flieschner
low risk: 4-6. 12m 6-8. 6 and 18m >8. 3, 9, 24m ``` high risk: <4. 12m 4-6. 6 and 18m 6-8. 3, 9, 24m >8. bx +/- pet ```
32
pinpoint nodules
``` must be dense if can see. barytosis. MZ silicosis. UZ stannosis. Even UZ and LZ alveolar microlithiasis. sand lung with obliteration of heart and diaph shadow talcosis ```
33
miliary nodules
ST density: febrile or afebrile Febrile: Tb, fungal, early HP Afebrile: CWP (MZ and spares bases and apicies), sarcoid (MZ and UZ), Miliary TB, Mets (LZ), HP High density: heamosiderosis (middle age male), silocisi, barytosis, stannosis, healed VZV
34
conglomeration of nodules
``` sarcoid silicosis. PMF secondary mets bronchoalveolar ca in situ Tb fungal HP EG lymphoid granulomatosis ```
35
reticular density cxr
``` acute or chronic. Acute: pulm odema. cardiacardiac or non infection. Viral, PCP, mycoplasma drug reaction pulm haemorrhage ``` Chronic: post infectious scars. Tb, PCP chronic interstitial oedema. MR/MS CTDs. Ank spon, RA, scleroderma (oesoph dilated) pulm haem inhalation. asbestosis (LZ), CW (MZ), HP (MZ), silicosis (UZ) sarcoid drugs. amiodarone (bright liver), chemo, rxt neoplasm. lymphangitis carcinomatosis, lymphatic spread, lymphoma idiopathic. UIP, TS, LAM, amyloid
36
lymphangitis spread ca
breast stomach thyroid
37
HRCT nodule distribution
Centrilobular, perilymphatic, random Centrilobular: TIB. infection No TIB. infection, HP, oedema, RB-ILD, adenoca, early LCH, vasculitis Perilymphatic: patchy. Sarcoid, silicosis, CWP, LIP, lymphoma, amyloid, perilymphatic spread ca Random: Haem mets, early LCH, Miliary TB, Miliary fungal, HP
38
Honeycomb
UIP Fibrosis sarcoid Chronic HP
39
reticulonodular
Lymphangitis carcinomatosis Silicosis Sarcoid
40
Crazy paving
``` GGO with interlob septal thickening Pulm alv protinosis ARDS PCP Bacterial pn Pulm.oedema NSIP RXT Alveolar sarcoid ```
41
Mosaic
sharply defined and geographical airtrapping- stays lucent on exp (should normally be more opac) any small airways disease, so ignore unless main finding constructive bronchiolitis asthma HP Vascular cause-oligaemia rather than airtrap (Pulm stenosis, congen heart rt to lt shunt, big PEs)
42
UIP pattern
definate must have all 4: 1. subpleural basal predomin 2. reticulation/traction bronchiectesis 3. honeycomb 4. absence of inconsistent findings possible UIP: no honeycomb ``` Inconsistent: UZ or MZ Peri bronchovascular Extensive GGO Profuse nodules Discrete cysts Diffuse mosaic/airtrap Consolidation ```
43
Causes of UIP
``` IPF CTD. RA (Scleroderma and polymyositis NSIP, sjogrens and RA LIP) Asbestosis HP CWP and silicosis Sarcoidosis Drugs. bleomycin, cyclophosphamide Bone marrow tx ```
44
Causes OP
``` Infection Drugs Fumes HP COP. idiopathic ```
45
NSIP
``` Basal and subpleural GGO Reticulation/fibrosis +/- cysts Homogenous. No normal lung between ``` younger than UIP (40-50s) inflammatory type. better prognosis fibrotic type. inflamm, RB-ILD, DIP, OP and LIP progress to
46
Causes NSIP
``` Drugs CTDs Idiopathic RB-ILD/DIP OP LIP ```
47
HIV Infections
CD4 >200. Tb, viral and bronchopn (GGO and TIB) CD4 <200. MAC, PCP, CD4 <100. CMV, Disseminated fungal (candida, cryptococcus, aspergilosis), lymphoma, Kaposi Chronic. Lymphoma, kaposis
48
Aspergillus
N immunity. Aspergilloma. fungal ball in pre existing cavity. CF, sarcoid, TB, emphysema Decreased immunity. angioinvasive aspergillosis. infiltrates bronchial aa and can disseminate kidneys, cns, git. nodules with GG halo airways invasive. infiltrates BM. wall thickening, bronchiolitis, TIB Hyperimmunity. ABPA. Chronic asthma, CF. Finger in glove mucous plugging.
49
Emphysema
Centrilobular. UL with central dot. Smokers. can cause pulm htn Pan lobular. LL. alpha 1 at. middle aged men. cirrhosis, panc ca and intracranial aneurysms Paraseptal. Smokers. Maran, IVDU, HIV
50
Primary lung ca
SCLC. Central. Neuroendocrine, local invasion into SVC, paraneoplastic. NSCLC. Adenoca, Large cell, Sq Adenoca. Peripheral. lobular or multiple small nodules. pseudo cavitation (bubbly), can be lepeidic. Non smokers Large cell. peripheral and >4cm Sq. cell. Central, cavitating, panc past, rib invasion
51
Primary lung cancer mets to
``` Brain Bone Adrenals LN Liver ```
52
Unilateral pleural effusion
Tumour. Mesothelioma, mets, bronchogenic ca, lymphoma Infection. Klebsiella, Empyem, parapneumonic, etc of subdiaph inf Chylothorax. ruptured or injured thoracic duct, tumour infiltration Haemorrhage. trauma, iatrogenic
53
Plural effusion
Transudate, exude, chylothorax or haemothorax Transudate. CCF, CRF, Meigs (ovarian tumor. Rt>lt), Liver failure Exudate. Protein >30. Infection, malig (lung, breast, ovary, lymphoma), infarct/PE, CVD (RA, SLE), Pancreatitis, subphrenic abscess, drugs (phenytoin) Haem. trauma, aneurysm, carcinoma, bleeding disorder
54
elevated diaphragm
``` Phrenic nn palsy. tumor, trauma, iatrogenic Subpulmonic effusion. diaph peaks lateral (medial peak = LL collapse) Liver or spleen enl subphrenic mass Eventration Ascities splint in from pain hemiplegia scoliosis ```
55
Empyema
``` obtuse angles with wall split rind C+ - pleural enhances late so do delayed scan (ie PV) air/fluid level biconvex cf crescentric *gram -ve, pneumococcus in kids, tb ``` Empyema necessitans. erodes into chest wall and OM ribs. +/- fistula
56
pleural ca+
``` old empyema old haemothorax talc pleurodesis asbestos silicosis ```
57
PTx
spontaneous. 20yo tall thin. ruptured subpleural bleb iatrogenic trauma lung disease. emphysema/bulla, CF, PCP, cystic lung disease, honeycomb, pn bronchopleural fistula. enl over time. don't resolve with chest drain alveolar rupture. asthma, ventilation, ards
58
Pleural mass
Mets. adenoca, breast and bronchus mesothelioma pleural fibroma. smooth, 2-15cm diam, pedicle and changes location on moving, c+ homogeneous. located effusion lipoma invasion from chest wall mass.. ewings fibro thorax. smooth wall cx thickening. prior Tb, empyema or haemothorax. v. high density with ca+ (cf meso)
59
Rib notching
``` Superior. Hyper PTH Osteogenesis imperfecta RA SLE Marfan NF ``` Inferior: Vascular collateral. SVC obst, AVM, Aortic coarct, TOF, absent pulm aa Neurogenic tumor. NF neurofibroma, schwannoma
60
Cardiac moguls
1. aortopulm window. Aortic aneurysm, HTN, ectasia 2. Above Lt main bronchus. Pulm stenosis, Pulm aa HTN. Concavity = pulm atresia, rt>lt shunt, TGA 3. Below Lt main bronchus. Lt atrial/appendage enl, coronary aa aneurysm, sinus valsalva aneurysm, cardiac aneurysm
61
Pulmonary HTN
``` Idiopathic. F child bearing age Anything causing hypoxia. Emphysema, chronic lung disease schistosomiasis mitral stenosis chronic PE Lt to Rt shunt. AD, VSD ```
62
Cardiac mass
``` Thrombus Myxoma. Lt atrium > Rt Lipoma Fibroelastoma Rhabdomyosarcoma. Assoc TS. Kids <1yo Sarcoma Mets. Melanoma ```
63
Pericardial mass
``` Primary. Mesothelioma, sarcoma, lipoma, teratoma Mets. Breast and lung Direct invasion from adj Pericardial cyst Pericardial effusion Pericarditis ```
64
Pericardial ca+
``` Pericarditis. Tb Trauma Rheum fever Malignant Renal failure Asbestos plaques myocarditis. rheum fever, MI, aneurysm ```
65
Thoracic outlet sx
``` 7th c rib non union 1st rib aberrant insertion ant scalene mm fibrous band supraclavicular tumour ```
66
cardiac wall outpouching
``` Ventricular aneurysm. often ca+ Enl lt atrial appendage Pericardial cyst Hydatid coronary aa aneurysm myocardial or pericardial 1ry or 2ry malig ```
67
Cardiomegaly
Cardiomyopathy. most xommon cause kids and young adults. Ischaemic, infective, Idiopathic, infiltration (sarcoid, amyloid), etoh, peripartum Pericardial effusion. globular, flask shape Multivalvular disease ASD. Congenital heart disease
68
Rt atrial enl
Rt heart border outpouching on PA. Loss retrosternal clear space on Lat ``` Rt heart failure TR/TS AF AVSD/ ASD Anomalous pulm vv return Rt atrial obst. myxoma ```
69
Rt Ventricle enl
Elevated cardiac apex PA Anterior prominence on Lat ``` TR/PR/PS ASD/VSD Anomalous pulm venous return Pulm HTN Acute PE ```
70
Lt atrial enl
3rd mogul, double rt heart border, elevated lt main bronchus, splayed carina on PA Prominent upper posterior heart border, oesoph impression, posterior displacement lt main bronchus on Lat. ``` MR/MS VSD PDA LV failure MV obst. myxoma ```
71
Lt ventricle enl
Cardiac apex down and out on PA Posterior inferior heart prominence on Lat ``` STEMI Dilated CM AR/AS MR HTN PDA ```
72
Honeycomb vs cysts
Honeycomb thick walled | cysts thin walled