Lung Pathology Flashcards

1
Q

Pathogenesis of asthma

A

 Sensitisation to allergen; followed by…
 Immediate phase = mast cell degranulation  mediator release  inc. vascular permeability, eosinophil and mast cell recruitment and bronchospasm
 Late phase = tissue damage, increased mucous production, muscle hypertrophy

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2
Q

Histology of asthma

A

Hyperaemia
 [Top right] Eosinophils and goblet cell hyperplasia
 Hypertrophic constricted muscle
 Mucus plugging and inflammation

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3
Q

Histology of COPD

A

 Dilatation of airways
 Hypertrophy of mucous glands
 Goblet cell hyperplasia

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4
Q

Causes of bronchiectasis

A

 Congenital (CF, ciliary dyskinesia

 Inflammatory (post-infectious, obstruction, 2nd to bronchiolar disease and interstitial fibrosis, asthma)

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5
Q

Histoogy of pulmonary oedema

A

 Intra-alveolar fluid on histology

 “Heart failure cells” = iron-laden macrophages (right)

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6
Q

Pathology of ARDS

A
  1. Capillary congestion
  2. Exudative phase
  3. Hyaline membranes
  4. Organising phase
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7
Q

Bronchopneumonia pathology

A

Patchy bronchial and peribronchial distribution, lower lobes, inflammation surrounding the airways themselves and is within the alveoli

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8
Q

Lobar pneumonia pathology

A
  • (1) Congestion Hyperaemia, Intra-alveolar fluid
  • (2) Red hepatization Hyperaemia, Intra-alveolar neutrophils (non-atypical)
  • (3) Grey hepatization (looks like liver) Intra-alveolar connective tissue
  • (4) Resolution Restoration normal architecture

90-95% pneumococci (i.e. strep)

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9
Q

Inflammation in atypical pneumonias

A

 Interstitial inflammation without the accumulation of intra-alveolar inflammatory cells

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10
Q

Pathogenesis of emphysema

A

Cigarette smoke inhibits A1AT- causes proteases to degrade the tissue causing permanent loss of alveolar parenchyma distal to terminal bronchiole

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11
Q

Causes of granuloma

A

TB, sarcoidosis, FB aspiration

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12
Q

Sarcoidosis lung involvement

A

 discrete epithelioid and giant cell granulomas, preferential distribution in upper zones with a tendency to peri-lymphatic and peri-bronchial  advanced disease becomes fibrocystic

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13
Q

Diagnosis of sarcoidosis

A

non-caseating granuloma, elevated serum ACE, hypercalcaemia (1a-hydroxylase)

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14
Q

Types of fibrosis interstitial lung disease

A

Idiopathathic pulmonary fibrosis
Extrinsic allergic alveolitis
Pneumoconiosis

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15
Q

IPF pathology

A
  • Macro = basal and peripheral fibrosis and cyst formation

* Micro = interstitial fibrosis (varying stages)

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16
Q

Diagnosis of IPF

A

 HR-CT ± biopsy diagnosis

17
Q

Which lung cancers are associated with smoking

A

Squamous cell carcinoma
Small cell carcinoma
Large cell

18
Q

Which lung cancer is not associated with smoking

A

Adenocarcnioma

19
Q

Features of Squamous CC

A

 Centrally located arising from bronchial epithelium  spread locally  metastasise late

20
Q

Features of adenocarcinoma

A
o	Peripheral (terminal airways) with multi-centric pattern 
o	Precursor lesion: atypical adenomatous hyperplasia 

 In smokers, the main mutations are K-ras, issues with DNA methylation and p53
 In non-smokers, EGFR mutations are very important (these are drug targets)

o Extra-thoracic metastases are COMMON and occur EARLY (80% present with metastases

21
Q

Histology of adenocarcinoma

A

 Gland formation
 Papillae formation
 Mucin

22
Q

Histology of large cell carcinoma

A

o Poorly differentiated tumours composed of large cells

23
Q

Features of small cell carcinoma

A

 Often CENTRAL and near the bronchi
 80% will present with advanced disease  very chemosensitive but VERY POOR PROGNOSIS
 May cause paraneoplastic syndromes (i.e. SIADH)

24
Q

Histology of small CC

A
	Small poorly differentiated cells 
	Common mutations: p53, RB1
o	Cytology:
	Small cells
	Ciliated normal respiratory cell
25
Q

Adenocarcinoma molecular targets

A
  • EGFR mutation (responder or resistance)
  • ALK translocation responds to Crizotinib
  • Ros1 translocatio
26
Q

Paraneoplastic conditions associated with lung cancer

A

ADH, ACTH, PTH