Odds & Ends Flashcards

1
Q

Most common primary tracheal malignancies

A

1) Squamous cell carcinoma
2) Adenoid cystic carcinoma (4th-5th decades, not associated with smoking, submucosal, circumferential/infiltrative growth)
3) Mucoepidermoid carcinoma (favour airways distal to the trachea)

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2
Q

5 main subtypes of pulmonary HTN and causes

A

1) PAH
PPH (idiopathic), familial, shunts, PVOD, PCH

2) Pulm venous HTN
Left sided heart disease

3) Pulm HTN ass. chronic hypoxemia
Chronic lung disease

4) Pulm HTN due to chronic PE
5) Pulm HTN from miscellaneous d/o (sarcoid, malignancy, fibrosing mediastinitis)

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3
Q

Imaging findings in PH

A

Enlarged PA (>2.9 cm), rapid peripheral tapering
Calcification in chronic setting
Other findings dependant on cause:
- Mosaic attenuation (esp. in CTEPH)

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4
Q

Possible causes of PVOD

A

Pregnancy
Drugs (esp bleomycin)
Bone marrow transplant

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5
Q

Plain film findings of PE

A

Fleischner sign - widening of pulm arteries due to clot
Westermark sign - paucity of vessels in the upper lobes
Hampton’s hump - airspace opacity from infarct

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6
Q

Timing and findings in radiation changes

A

Radiation pneumonitis - Geographic ground glass at radiation port, sharp margins, can start 1 month post (4-12 weeks post rads), most severe 3-4 months post; can be positive on PET/CT

Radiation fibrosis - 6-12 months post radiation, fibrosis and traction bronchiectasis in rad port

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7
Q

Causes of exudative effusion

A

Infection - Parapneumonic, empyema, TB
Mesothelioma
Pleural mets
Collagen vascular disease - i.e. rheumatoid

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8
Q

What is post-pneumonectomy syndrome?

A

Compression of the airway, central bronchus after pneumonectomy, more commonly involves the left mainstem bronchus after RIGHT pneumonectomy

Often occurs in younger patients, less than 1% of cases

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9
Q

Possible appearances of drug reaction

A

OP, NSIP, HP, AIP/ARDS, Hemorrhage

Treat with steroids, can flare after stopping these

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10
Q

What is talcosis? Imaging findings?

A
  • Filler in oral tablets
  • Hyperdense micronodules <1 mm, or conglomerate masses like those seen in silicosis
  • If panlobular emphsema present - more likely to be from Ritalin injection
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11
Q

DDx pleural calcification

A

Asbestos (bilateral, small plaques)
Prior hemothorax
Prior infection (particularly TB)
Talc pleurodesis

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12
Q

What is Kaplan syndrome?

A

Rheumatoid pneumoconiosis (i.e. patients with rheumatoid who also have CWP, silicosis, etc. )

Large necrobiotic nodules, with more numerous additional nodules and usual changes of pneumoconiosis

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13
Q

What is Lofgrens syndrome?

A

Acute presentation of sarcoid

  • lymphadenopathy
  • erythema nodosum
  • polyarthralgias
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