Differentials Flashcards

1
Q

Differential diagnosis for multiple round pulmonary lesions in elderly patient?

A

V - Mulitple AVMs = hereditary haemorrhage telangiectasia
I - Abscesses, (s. aureus), histo, hydatid
T - N/A
A - Wegener’s, rheumatoid, progressive massive fibrosis
M
I - N/A
Neoplastic: Metastases, Breast, thyroid, kidney, GI - lower lobes. Multiple synchronous lung cancers, benign metastasing tumours - fibroids, meningiomas, pleomorphic adenomas
Congenital: -

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2
Q

123

A

123

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3
Q

Causes of centrilobular micronodules

A

Infection: Viral, mycobacterial
Aspiration
Inflammation - hypersensitivity pneumonitis, respiratory bronchiolitis

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4
Q

Causes of tree-in-bud micronodules

A

Issue affecting the bronchi, vessels or axial interstitium

Infection –> bronchiolitis:
- Mycobacterial
- Viral
- Bacterial pneumonia
- Aspiration

Neoplastic
- Endovascular met - breast, stomach
- Lymphangitis carcinomatosis

Connective tissue disorders - RA, Sjogren’s

Inflammatory: Bronchiolitis obliterans (post-transplant), diffuse pan-bronchiolitis (Asians), follicular bronchiolitis (BALT)

Congenital - CF, immotile cilia syndrome

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5
Q

Causes of diffuse cystic lung disease

A
  • Pulmonary Langerhans cell histiocytosis (young adults, cigarettes) - sparing of lower lobes and medial middle lobe/lingula - “costophrenic sulci”
  • LAM - women of childbearing age - multiple cysts, no zonal predilection
  • Tuberous sclerosis
  • Birt-Hogg-Dube - low lobe predominant, cigar shaped cysts
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6
Q

Causes of non-diffuse cystic lung disease

A

V - N/A

I - Post-infective:
- Bacterial pneumonia (staph aureus, strep)
- Pneumocystis jirovecii
- Hydatid cyst (fluid filled, air)

T - Post-traumatic:
- Lung laceration

A, M, I - N/A

Neoplastic:
- Post treatment of lung mets
- Cystic lung metastases - colonic, subtypes of sarcoma

Congenital:
- CPAM - single multi-loculated cyst
- Bronchogenic cyst

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7
Q

Cavitating lung lesions (gas-filled space within mass/nodule/consolidation)

A

Vascular
- Infarction - apical predominance - compared to lower segment predilection of non-cavitating infarcts

Infective:
- Staph aureus/Klebsiella
- TB
- Septic emboli
- Aspiration - associated with foreign body e.g. tooth
- Infection of pre-existing bulla/cyst/sequestration
- Hydatid, amoebiasis

Trauma:
- Haematoma, traumatic lung cyst

Autoimmune/inflammatory:
- Wegener’s granulomatosis
- Rheumatoid nodules
- Sarcoidosis - later stages

Metabolic:

Iatrogenic: N/A

Neoplastic:
- Lung cancer - predilection for UL - more common in SCC
- Metastases - SCC, colon, sarcoma
- Lymphoma

Congenital: N/A

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8
Q

Miliary distribution of micro-nodules

A

Soft tissue density:
- Infection: Miliary infections (TB or fungal (crypto, histo))
- Papillary thyroid carcinoma
- Sarcoidosis - upper zones (fibrosis/bronchiectasis), hilar adenopathy
- Pneumoconioses - coal worker’s

High-than soft tissue density
- Healed varicella infection
- Haemosiderosis
- Silicosis - sparing of bases and apices

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9
Q

Fibrosing mediastinitis differentials, how to distinguish?

A

DDx are malignancies - Low T2 on MRI can be useful to differentiate from these

Can be indistinguishable from sclerosing non-Hodgkin’s lymphoma in the absence of

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10
Q

Solitary pulmonary lesion differentials

A

Vascular: AVM
Infection: Granuloma (TB, histo), round pneumonia, hydatid,
Trauma: Haematoma
Autoimmune: Wegeners, RA
Metabolic: N/A
Iatrogenic: N/A
Neoplastic: Benign (Hamartoma, carcinoid) or malignant (lung primary or solitary met)
Congenital: LN, bronchopulmonary sequestration, bronchogenic cyst

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11
Q

Upper zone predominant fibrosis

A

Old TB
Silicosis/pneumoconiosis
Chronic hypersensitivity pneumonitis
Radiation
Ankylosing spondylitis
Pleuroparenchymal fibroelastosis

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12
Q

Causes of upper zone bronchiectasis

A

CF
TB

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13
Q

Causes of mid-zone bronchiectasis?

A

Non-tuberculous mycobacterial infection
Middle lobe syndrome in children

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14
Q

Causes of central bronchiectasis?

A

ABPA
Tracheobronchomegaly - Mounier Kuhn syndrome
CF

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15
Q

Cases of lower-zone bronchiectasis?

A

Aspiration/Post-infective
Primary ciliary dyskinesia
Immunodeficiency: Hypogammaglobulinaemia

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