Localisation of Pathologies
- Respiratory Epithelium Types
Location | Epithelium Type |
Nasal mucosa till Proximal bronchiole | Pseudostratified ciliated columnar epithelium |
Terminal bronchiole | Ciliated cuboidal epithelium • No goblet cells • Epithelium change • No hyaline cartilage from here |
Respiratory bronchiole | Non-ciliated cuboidal epithelium |
Alveolus | Simple squamous epithelium |






- Air bronchogram sign:
- Differentiate between parenchymal and extra parenchymal pathologies.
- Seen when:
- The lungs are white.
- The bronchi is patent (containing air - appears black).
- Seen in intraparenchymal pathologies:
- Consolidation.
- Hyaline membrane disease.
- Pulmonary edema
- Absent in
- Mediastinal mass
- Pleural effusion
Consolidation vs Collapse


Obstructive Lung Diseases (OLDs)

COPD (Chronic Obstructive Pulmonary Disease)

- COPD primarily encompasses Emphysema and Chronic Bronchitis.
- Both heavily associated with smoking.
- Permanent damage to airways distal to the terminal bronchioles.
- Damaged structures (collectively RDS):
- Respiratory bronchiole
- Alveolar duct
- Alveolar sac
Microscopic Finding:
- "floating septa" due to broken walls.



Types:
Type of Emphysema | Affected Part | Lobe Involved | Common Association |
Centriacinar | Central part (respiratory bronchiole) | Upper lobe | Smokers Most common clinically |
Panacinar | All of RDS (including alveoli) | Lower lobe | Alpha-1 antitrypsin deficiency |
Distal Acinar | Distal part (alveolar duct and sac) | ㅤ | Can cause spontaneous pneumothorax |
Irregular | Irregular damage (patchy involvement) | ㅤ | Most common histologically (on autopsy) |



- "pink puffers".
- Physiology:
- Inhalation is fine → exhalation of CO2 is problematic → air trapping → enlarged lungs.
Radiological Finding:
- Flattening of the diaphragm.

Chronic Bronchitis


- Blue bloaters
- Definition:
- Productive cough
- for at least 3 months in two consecutive years
- with other causes ruled out.
- Cyanosis (blue) → due to hypoxemia and hypercapnia.
- Obesity + edema (bloater) → right heart failure (cor pulmonale).
- Association:
- Primarily smoking → increased mucus production.
- Infections:
- M/c H. influenzae in COPD patients.
- Reid Index:
- Ratio of submucosal glands / wall thickness.
- In chronic bronchitis is > 40%
- Normal Reid Index is < 0.4.

A/w cor pulmonale
- M/c chronic bronchitis > emphysema.
- PAH + right-sided heart failure
CXR

- Hyperinflated lungs.
- Flat diaphragm.
- Tubular heart.
- Barrel chest on lateral CXR.
- DOC: Tiotropium
- MOA: M3 Antagonist
- Treats bronchoconstriction due to:
- Parasympathetic overactivity (reversible component)
- Fibrosis/sclerosis (irreversible component)
- Side Effects
- Dry mouth
- Worsening of BPH
VLABA → COPD only
- Olodaterol
- Vilanterol
- Carmoterol
- Karma (Carmeterol) for Old (Olodaterol) Villains (Vilanterol)
New drugs COPD :
- Roflumilast : PDE4 ⛔
- Ensifentrine : Both PDE3 ⛔ and PDE4 ⛔
- Rough (Roflumilast) Siphon (Ensifen)
Asthma
Genetics:
- Gene for atopy: Chromosome 5q gene Polymorphism
- At birth → TH2 Phenotype
- Normally
- switch to TH1 phenotype
- due to exposure to many outdoor antigens
- TH1 phenotype → Asthma disappears.
- No exposure to allergens
- Persistence of TH2 phenotype.
- Persistence of TH2 phenotype → Asthma persists.
- Associations:
- IL-13, ADAM33 gene polymorphisms.
- Note: mutation of ADAMTS-13: TTP
- Type 1 hypersensitivity (allergic) reaction.
- IL-5 → Eosinophil mediated Pathology.
Features of Asthma:
- Type I Respiratory Failure:
- No CO2 retention seen.
- No Type II respiratory failure.
- No parenchymal involvement.
- No diffusion defect.
- Normal to ↑ DLCO.
Sputum Microscopy (The Three C's):

- Charcot-Leyden crystals:
- Needle-shaped crystals made of galectin-10
- derived from eosinophils.
- Eda charley, needle vach easy aytt kalakku
- Creola bodies:
- Clusters of epithelial cells.
- Sloughed mucus epithelium.
- Curschmann spirals:
- Whorled Mucus Plugs.

Lung Finding:
- Shows airway remodeling.
Micropathological Changes:

- Patchy Epithelial Necrosis
- Sub-Mucosal Glandular Hyperplasia
- Hypertrophy of bronchial smooth muscle
- Reid's Index is normal.

Classification | Symptom Frequency | Night Awakenings | Impact on Activity | FEV1 (% Pred.) | PEFR Variability | Recommended Treatment (GINA 2019) |
Intermittent | < 2 episodes per month | ㅤ | None | ㅤ | ㅤ | Relievers (LABA) + ICS (if needed) |
Mild Persistent | ≥ 2 episodes per month | ≥ 1 night/ month | Minor limitation | > 80% | < 30% | Relievers (LABA) + Low dose ICS (Daily) |
Moderate Persistent | Daily, not continuous | ≥ 1 episode / week | Some limitation | 60-80% | > 30% | Medium dose ICS (Daily) OR Low dose ICS (Daily) + LABA (Formetrol) |
Severe Persistent | Continuous | Frequent | Significant limitation | < 60% | > 30% | High dose ICS (Daily) + LABA (Formetrol) |
GINA (GLOBAL INITIATIVE FOR ASTHMA) GUIDELINES

Therapy Type | Drug of Choice (DOC) |
Acute Attack (Rescue Therapy) | Inhalational formoterol + Low dose inhaled corticosteroids |
Maintenance Therapy | Formoterol + Low dose ICS |
Brittle Asthma
- Frequent, sudden, and life-threatening attacks
- Occurs despite appropriate therapy
Types of Brittle Asthma
Type 1 | Type 2 |
Persistent variability in PEFR | Normal or near-normal PEFR |
Wide day-to-day fluctuations | Sudden unpredictable exacerbations No obvious trigger |
Management • Oral steroids • Infusion of bronchodilators • Dietary exclusion of allergens | Management • Respond only to subcutaneous epinephrine |
Extrinsic Asthma | Intrinsic Asthma |
• Atopic → childhood onset • Boys > Girls | • Adult Onset |
• Type I Hypersensitivity | • Negative Skin Test |
• ↑ IgE levels – Eosinophils | • Normal IgE levels |
Associated with: • Allergic Rhinitis • Atopic Dermatitis | Super antigen: • Staph Aureus Enterotoxin |
MC allergen : • Dermatophagoides (House dust mites) | Samter's Triad : • Adult onset Asthma • Aspirin Intake • Nasal Polyps • Bad Prognosis • Males = Females |
- Airway Hyperresponsiveness assessed by:
- MCT (Methacholine Challenge Test).
- IgE levels:
- RAST (Radio AllergoSorbent Test).
- Non Invasive Test to assess airway inflammation:
- Fractional Exhalation of Nitric Oxide (FeNO).
Pulmonary Function Tests:
- ↓ FEV1/FVC ratio.
Response | ㅤ |
Response to inhaled β2 agonist | • ↑ 12% in FEV1, • ≥ 200mL ↑ • β2 → 12 |
Diurnal variation in PEFR/FEV | • ↑ > 20%. • 24 hrs → 20 |
Exercise challenge | • ↓ > 15% in FEV1. |
Acute Severe Asthma | Life-threatening Asthma |
Dyspneic, Speaks in words | Altered mental status with drowsiness. |
Agitated Patient | Exhaustion, Cyanosis |
Loud wheeze throughout Respiration | Silent Chest (Absent chest sounds) Mute |
Respiratory Rate = 30/min | RR > 30bpm (in adults) RR > 60bpm (in children) |
Peak Expiratory Flow 25-40 ml/min | PEFR < 25% predicted or best. |
Accessory muscles are used | Poor respiratory effort. |
Heart rate > 120 : Tachycardia | Hypotension, Arrhythmia, Relative Bradycardia |
Pulsus Paradoxus (+) | Sp02 < 90%. PaO2 < 8 kPa; < 60mmHg of Hg PaCO2: < 40 mmHg. Paradoxial ◦ PaCO2 is normal (4.6-6 kPa) ◦ Paradoxical Breathing ◦ Relative Bradycardia ◦ No pulsus paradoxus |
Peak expiratory flow meters

- Portable, hand-held devices
- Used at home for monitoring PEFR
- Increase diurnal variability of PEFR (peak expiratory flow rate) >13%
Treatment of asthma in children
- As per the latest GINA (Global Initiative for asthma),
- All children with Bronchial Asthma
- daily dose ICS + SABA
- either Symptom driven or daily.
- No role of SABA only Rx in managing acute exacerbations
- It increases r/o exacerbations
Metered dose inhaler

- Used in drug delivery in children with bronchial asthma
- Parts
- Blue colored structure:
- Metered dose inhaler,
- Contains bronchodilator
- White-colored structure:
- Spacer,
- Must since it improves in drug delivery
- Baby mask:
- Required in < 4 years age children.
Management of status asthmaticus in a child
- Medical emergency
- Also known as acute severe asthma
- The pulmonary index score is used for the assessment of the severity
- Primary management
- airway, breathing and circulation
- (Chest x-ray and ABG to look for ventilation therapy)
- Start oxygen therapy and admission
- Continuous nebulization
- levosalbutamol/MDI
- Start systemic steroids
- Inj. hydrocortisone → f/b oral prednisolone
- Ipratropium nebulization can be used
- In case of no improvement:
- Inj. Magnesium sulfate,
- theophylline
- ketamine
Bronchiectasis



- Definition: Dilation of the bronchi and bronchioles.
- Causes:
- Genetic: Most famously, Kartagener Syndrome.
- Acquired: Obstruction (e.g., foreign body) or bacterial infection (e.g., sepsis).
- Kartagener Syndrome:
- Defect: Dynein defect of cilia.
- Dynamic (Dynein defect) Kart (Kartagener)
- Triad:
- Bronchiectasis
- Sinusitis
- Situs inversus (e.g., dextrocardia)
- Important Additional Finding: Associated with male and female infertility.
- Location:
- M/c in Left Lower Lobe
- LL > UL
- Investigation:
- HRCT is the definitive investigation.
- Radiological Finding: Classic "tram track appearance".
- Note: A "tram track appearance" can also be seen on microscopic examination in MPG type 1 (a renal disorder).
- MP (MPGN) runs in a Kart (Kartagener) through Tram track ()

- Dilatation of bronchi.
- Normally, bronchus tapers down peripherally.
- In Bronchiectasis
- no tapering → bronchi remain parallel
- Tram track sign
- Signet ring sign:
- Vessel adjacent to the dilated bronchi.

Kartagener Syndrome
- Bronchiectasis associated with situs inversus
- Kartagener's syndrome

Interstitial Lung Disease


- Military (Miliary) people
- get TB
- Laugh (Loeffler’s)
- Heal by eating chicken (healed varicella)
- make History (Histoplasmosis)
- Presentation:
- Usually a female patient
- dry cough, shortness of breath
- associated with connective tissue disorder.
- M/c type
- Idiopathic pulmonary fibrosis

- IOC - HRCT.
- UIP/IPF pattern
- Honeycombing pattern +
- Basal Lower lobe dominance +
- Traction bronchiectasis
- Ni thanna (Nintendanib) Feni done (Pirfenidone) ayi → lung fibrosis ayi (IPF)
- TGF α → KGF α → Menetriers disease
- TGB β → KGF β → drink Feni
- Ninte Dani → PD Girl Friend (PDGF)

Nintendanib
Crazy pavement appearance:

- Interlobular septal thickening is seen with ground glass opacity.
- no air filled cavities are seen.
- Seen in Pulmonary alveolar proteinosis >>> COVID 19
- Mnemonic: Crazy Pappu (PAP) in pavement
Cystic Bronchiectasis

- Some of these dilated bronchi contain mucus.
- Bronchi appears as cysts.
- Bunch of grape appearance.
Pulmonary Alveolar Proteinosis
- Interstitial lung disease
- Due to defective pulmonary macrophage function
- Leads to accumulation of surfactant in alveoli and bronchioles
- Autoantibodies against GM-CSF → most common cause
- Clinical features
- Progressive dyspnea
- Cough with chunky, gelatinous sputum
- PAS-positive
- Histology
- Alveoli filled with:
- Pink, Dense, Homogeneous, Amorphous material
- Alveolar walls intact
- Surfactant proteins:
- Demonstrated by IHC
- HRCT: Crazy pavement appearance
Pneumoconiosis

- Pneumoconioses are occupation-related lung diseases.
- Mostly involve upper lobe of lung.
- Exception
- Asbestosis → affect lower lobe
- Restrictive lung diseases.
- All notifiable except bagassosis.
Range of Dust Particles
Size (micron) | Effect | ㅤ |
5-10 | Lodged in upper respiratory tract | ㅤ |
3-5 | Lodged in lower respiratory tract | Cause pneumoconiosis |
1-3 | Lodged in alveoli | Cause pneumoconiosis |
<1 | Diffusible | ㅤ |
- Note: 1-5 micron sizes cause pneumoconiosis
Types
Disease | Particle | Source |
Silicosis | Silica | • Sand stone, granite, pottery and ceramic industry, • gold, mica and steel industry. |
Asbestosis | Asbestos | • Asbestos cement factory, fireproof textiles. |
Anthracosis (Black lung) | Coal dust | • Coal mines. |
Byssinosis | Cotton dust | • Textile industries. • Cotton business |
Bagassosis | Sugar cane dust (Bagasse) | • Inhalation of Thermoactinomyces sacchari • Bag of sugar |
Silicosis vs Asbestosis
ㅤ | Silicosis | Asbestosis |
Cause | Silica dust | Asbestos fiber |
Affects | upper lung zone | Lower lung zone |
Leads to | Alveolitis | Bronchiolitis |
X-ray | Snow storm appearance | Ground glass appearance |
Association | TB complication | Bronchial Ca → M/C Mesothelioma → Most specific |
ㅤ | silica - snowstorm | AsBastosis - Base, Ground Bronchilolitis, |
Harmful Chemicals
Chemicals | Disease |
Benzene, Ethylene Oxide | Leukemia |
Benzidine | Bladder cancer |
Beryllium, Cadmium, Chromium, Radon, Silica, ionizing radiation, Nickel | Lung cancer |
Arsenic | Skin, lung, liver cancer |
PAH (Polycyclic Aromatic Hydrocarbon) | Skin, scrotum and lung cancer Aromatic - skin , scrotum, lungs |
Vinyl chloride (PVC plastic) | Liver cancer |
Wood dust, Nickel, Chromium | Nasal sinus problems Different color() nikker() itt wood() panikk poi sinusitis vann |
Silicosis

- Most common pneumoconiosis.
- glass industry, sandblasting industry
- Progressive massive nodular fibrosis → Upper lobe
- Lymph Node:
- eggshell calcification in the lymph nodes.
- increased risk of TB and lung cancer.
- Silly (Silicosis) people are like egg shell () and glass ()
- Egg (Egg shell) beaten on a glass (glass industry) → bubble (nodular fibrosis) when heat
- Egg shell calcification:
- Peripheral Calcification around lymph nodes
- hilar lymphadenopathy
- also in silicosis., Sarcoidosis, Post radiation therapy lymph nodes
COALWORKERS PNEUMONIA
- Industry Association: Related to the coal industry.
Progression (Three Steps):
1. Anthracosis:
- Just black lungs with no symptoms.

- Definition: Inhaled carbon.
- Appearance: Black color lungs.
2. Simple CWP:
- Development of centriacinar emphysema.
- Mnemonic: Coal smoke has 'S' sound, like smokers, hence centriacinar
3. Complicated CWP:
- Results in fibrosis.
- Kaplan Syndrome
- CWP + rheumatoid arthritis.
- Note: Felty syndrome

- X ray
- Upper lobes opacities
- We Felt (Felty syndrome) pain fo RA () ENT pg → We gave him a cap (Caplan)
- NOTE:
- Erasmus syndrome: CWP + Systemic sclerosis
- Erase & Cap → CWP syndromes
- EraSS → Systemic sclerosis
ASBESTOSIS


- Location:
- Affects the lower lobe of the lung.
- Mnemonic: "Basetosis" for base/lower lobe
- Forms:
- Amphibole / Crocidolite → Good Prognosis
- Mnemonic: Amphibian, like a crocodile, lives in land and water
- Serpentine / Chrysotile.
- Snake → Cry
- High-resolution computed tomography (HRCT)
- "honeycombing"
- Associated Cancers:
- Most common cancer:
- Adenocarcinoma lung.
- Most specific cancer:
- Mesothelioma → Frozen Hemithorax (Hallmark)

- Associated with
- Shipyard industry
- Cement industry
- Mnemonic: Basetosis → Mesayude (Mesothelioma) adiyil (adenocarcinoma) Dumbell (asbetos bodies), made of iron (ferruginous bodies) → long vili vilichu (branched long filaments on E/M)
- Microscopic Finding:
- Characterized by pleural plaque and pleural nodules containing dumbbell-shaped asbestos bodies (ferruginous bodies).


- Occupational lung disease - M/c shipyard industry.
- Mnemonic: Asbestos → Holly leaf → comet tail
- M/c radiological finding:
- Calcified pleural plaques - Holly leaf sign.
- Base of lung/Diaphragmatic pleura is affected.

- On CT:
- Comet tail sign:
- Rounded opacity
- vessels pulled towards it
- seen in round atelectasis.
- The white opacity seen along the pleura are the plaques.

- Can give rise to Mesothelioma.
Note: Other structures with dumbbell shapes in pathology/radiology:

- Calcium oxalate monohydrate crystals (renal pathology).
- Spinal schwannoma (radiology).
- Pox virus DNA (microbiology).
- Byssinosis:
- Exposure to cotton or organic dust.
- Mnemonic: Business → cotton
- Bagassosis:
- Exposure to sugarcane dust.
- Mnemonic: Bagil sugar
- Berylliosis:
- Exposure to beryllium.
- Microscopic Finding: Shows non-caseating granulomas, Monocytic
- Jewellery /dental alloy
- Granulomatosis → Similar to sarcoidosis
- BeLPT → Beryllium Lymphoproliferative test
- HLA-DP
- Cobalt exposure
- Diamond industry
- Giant cell interstitial pneumonitis
- cobelt - belt ilu diamond it is giant
- Stannosis:
- Exposure to tin.
- Siderosis:
- Exposure to iron.
Extrinsic Allergic Alveolitis / Hypersensitivity Pneumonitis
Definition
- Repeated inhalation of organic antigens in dusts.
Pathogenesis :
- Both Type 3 and Type 4 hypersensitivity.
Causes & Examples
Lung Condition | Antigen |
Bird fanciers' lung | Avian proteins |
Farmer's lung | Saccharopolyspora rectivirgula spores |
Malt workers' lung | Aspergillus clavatus |
Mushroom workers' lung | Thermophilic actinomycetes |
Investigations
- Chest X-ray:
- Diffuse micronodular interstitial shadowing.
- CT
- Ground glass appearance

- Broncho-alveolar lavage:
- Lymphocytosis.
- Blood: NO eosinophilia.
Differences between HP & Allergic Bronchopulmonary Aspergillosis (ABPA)
Feature | Allergic Bronchopulmonary Aspergillosis (ABPA) | Hypersensitivity Pneumonitis (HP) |
Pathology | - Colonisation of airway - Eosinophilic inflammation - Hypersensitivity (I + III) | - Non caseating granulomas - Lymphocytic inflammation - Hypersensitivity (IV > III) |
Radiographic Features | - Bronchiectatic changes - Migratory infiltrates | - Diffuse infiltrates → Reticulonodular opacities - Bilateral GGD & nodular opacity - CT: Mosaic tiles attenuation |
Skin test reaction to aspergillus antigens | +ve (A. fumigatus) | +ve (A. clavatus) |
Peripheral eosinophilia | +ve | -ve |
IgG Aspergillus precipitins (Type III hypersensitivity) | +ve | +ve |
Serum IgE levels | ↑↑ (Significantly increased) | Normal |
Aspergillus lungs:

- A fungus with septate and acute angle branching hyphae.
- Can cause:
- Allergic Bronchopulmonary aspergillosis (ABPA).
- Aspergilloma.
- Angio invasive aspergillosis.
ABPA:
- Dilated central bronchi filled with mucous - Finger in glove sign.



Aspergilloma:
- Seen when there is a pre existing cavity in the lung.
- Air crescent sign or monod sign.
- Prone CT to confirm aspergilloma:
- fungal ball is mobile
- comes to the dependent position.

Angio Invasive Aspergillosis:


- Central infarct surrounded by GGO - Halo sign.
- i.e. white consolidation surrounded by ground glass opacity.
- Seen in immunocompromised patients.
- Voriconazole
Mucormycosis lungs
- Also called: Black fungus
- Reverse HALO sign (Atoll sign) → centre dark, periphery light




- Reverse halo sign on CT
- Neutropenia
- Immunocompromised
- Hyphae: Aseptate, Right angle, Broad, ribbon-like
- Culture:
- Lid-Lifters (SDA)
- May be negative d/t Hyphal fragility (killed by tissue homogenisation)
- Lid lift cheyyumbo mukki povum
- Treatment
- Surgical resection
- Amphotericin B +/- Posaconazole
- Mucus pasha pole - Posaconazole
- Negative Staining Group:
- Blastomyces, Mucorales, Cryptococcus
- Banglore Medical College

ARDS


Pulm edema → 1st sign → cephalisation
Criteria
- ARDS is known by various names:
- Acute Lung Injury
- DAD
- Blast Lung
- Acute Alveolar Injury
Berlin Definition 2012

- Acute onset:
- Within 1 week of clinical insult/worsening respiratory symptoms.
- Chest X-ray:
- Bilateral alveolar/interstitial infiltrates not explained by effusion/collapse/nodules.
- Non-cardiogenic:
- Normal ECHO.
- Oxygenation:
Severity | PaO₂/FiO₂ |
Mild | 200 - 300 |
Moderate | 100 - 200 |
Severe | < 100 |
Factors Preventing Pulmonary Edema
- Retained intravascular protein.
- Interstitial lymphatics drain fluid.
- Tight junctions between epithelial cells.
Etiology
- Primary ARDS:
- Pulmonary sepsis.
- Massive blood transfusion.
- Acute pancreatitis.
- Transfusion-Associated Lung Injury (TRALI).
- Smoke inhalation.
- Drowning.
- Post-surgery.
- Secondary ARDS:
- Non-pulmonary sepsis (UTI, surgical site infection).
- Major trauma/burns.
Pathogenesis
- Toxin/sepsis → Alveolar epithelial injury → Release IL 1, IL 6, TNF α → Neutrophil recruitment and Damage of Capillary endothelium → Protein + Fluid coming out of endothelium → Air spaces filled with bloody proteinaceous fluid with loss of Surfactant → Pulmonary Edema → Hypoxia
Pathological Phases

- 1. Acute Exudative Phase (1st week):
- Diffuse alveolar damage (DAD):
- Interstitial + alveolar edema.
- Eosinophilic hyaline membrane deposition is the hallmark.
- Also known as hyaline membrane disease.
- 2. Fibroproliferative Phase (2nd week).
- 3. Fibrotic Vasoconstriction (3rd week).
Clinical Features
- Rapid onset dyspnea.
- Hypoxemia.
- Bilateral crackles: Diffuse pulmonary infiltrates.
- Tachypnea, tachycardia, diaphoresis.
- Pulmonary hypertension: Due to hypoxemic vasoconstriction.
Mechanical Ventilation
- Mainstay of treatment.

- Inverse ratio ventilation with inspiration.
- Prone ventilation.
- Permissive hypercapnia.
VILI (Ventilation-Induced Lung Injury)
Pathogenesis | Treatment |
Volume trauma: • ↑ Lung volume → Alveolar injury | Low tidal volume ventilation. (High frequency ventilation) |
Barotrauma: • ↑ Transpulmonary pressure | Low plateau pressure. (Low driving pressure) |
Atelectotrauma: • Collapse and de-collapse during tidal breathing | High PEEP |
Respiratory Failure
Type | Key points |
Type I Acute hypoxemic respiratory failure | • Low pO2 • Normal / low pCO2 |
Type II Hypoxemia with hypercapnia | • Low pO2 • High pCO2 |
Type III Peri-operative respiratory failure | • Seen after general anesthesia • Due to decreased functional residual capacity |
Type IV Shock-related respiratory failure | • Hypoperfusion of respiratory muscles • Seen in cardiogenic shock |
Pleural Effusion
(Light, REM and PEM)


- IOC - USG.
- Best X-ray view: Ipsilateral decubitus view.
- Light’s criteria for exudative effusion:
- Pleural fluid protein/serum protein >0.5
- Pleural fluid LDH/serum LDH >0.6
- Pleural fluid LDH >2/3rd upper reference limit of normal for serum.
Pleural effusion vs Hydropneumothorax

- Pleural effusion:
- Ellis's curve.
- Blunting of costophrenic angle.
- Hydropneumothorax:
- Horizontal air fluid level.
- Lateral decubitus X-ray
- Done for pleural effusion.
- Fluid comes to the dependant side.

- Pleural effusion signs:
- Most sensitive
- USG (5 - 10 mL) >
- I/L lateral decubitus > Lateral > CXR PA erect > Supine (500 ml)
- On chest X-ray:
- Ellis's curve.
- Blunting of costophrenic angle.
- due to accumulation of fluid.
- On CT scan (in supine):
- Fluid gravitates posteriorly.
- Appears gray in color.
- Most sensitive investigation:
- USG.

Infected pleural effusion (empyema)


- Empyema causes thickening of surrounding pleura:
- Split pleura sign.


Chylothorax
Chylothorax
- L subclavian vein catheterization
- Lymphatic leaks
- Triglyceride > 110 mg/dl

Pseudo chylothorax
- Seen in RA
- Normal TG → Cholesterol crystals +
Pulmonary Thromboembolism (PTE)

Causes of Thrombosis
- Inherited:
- Factor V Leiden mutation – most common.
- Acquired:
- Antiphospholipid antibody syndrome – most common.
- Nephrotic syndrome.
- Post-orthopedic surgery.
- Malignancy – adenocarcinoma.
- COPD.
- Pregnancy – pelvic veins.
Sites of Thrombosis
- Deep veins – most common femoral vein (supra-popliteal).
- Calf veins.
- Pelvic veins – in pregnancy.
Types of Pulmonary Embolism
- Massive – Hypotension present.
- Submassive – No hypotension, ± RV dilatation.
- Non-massive – No hypotension, no RV dilatation.
Symptoms
- Most common – Unexplained dyspnea.
- Syncope.
- Pleuritic chest pain.
- Cough with hemoptysis.
- Sudden cardiac death.
Risk Assessment
- Well’s score – assesses likelihood.
- Score > 4 → CTPA
- Score < 4 → D dimer


Diagnosis
- CT Pulmonary Angiography (CTPA) – gold standard.
- D-dimer – for low-risk patients.

Pulmonary Embolism Radio



• RV free wall → Hypokinetic
• RV Apex → Hyperkinetic
- Predisposing factor: DVT — Bedridden patients/immobilized patients.
- Screening investigation: D-dimer (raised).
- IOC - CTPA/CECT.
- Contrast filling defect is seen.
- X-ray Signs
- Palla sign: Enlarged right descending pulmonary artery
- Hampton's hump: Infarct formation.
- Westermark sign: Focal oligemia.


Pneumonia
MCC | Organism |
Typical CAP | S. Pneumonia |
Atypical CAP | Mycoplasma |
HAP (> 48hrs of admission) | Gram -ve |
VAP (> 48hrs of ventilation) | • Early: S. Pneumonia • Late: Pseudomonas • Nowadays: Acinetobacter |
CURB-65 Scoring


WHO IMNCI PROTOCOL



- Cough/cold:
- No pneumonia.
- Home care advice.
- Fast breathing/chest indrawing:
- Pneumonia.
- Oral amoxicillin/home care advice.
- Reassessed after 48 hours.
- If the child has worsened, refer to a higher center.
- General danger signs:
- Severe pneumonia/very severe disease.
- First dose antibiotic/referral for injectable antibiotic
- 1st dose of Inj. Ampicillin and Gentamycin
SAANS PROTOCOL:

- Social Awareness & Action to Neutralize Pneumonia Successfully.
- Launched in 2019 to reduce deaths due to childhood pneumonia.
- For 2-59 months child with cough +/- difficult breathing.
Management
Condition | Signs → SAANS Protocol |
Severe pneumonia/ very severe disease | General danger signs • Convulsions • Lethargy • Inability to drink or breastfeed • Persistent vomiting • Unconsciousness • Stridor in a calm child OR Chest indrawing |
Pneumonia | Fast breathing: - < 2 months: ≥ 60 breath/min - 2–11 months: ≥ 50 breaths/min - 12–59 months: ≥ 40 breaths/min |
No pneumonia/cough or cold | No signs of severe pneumonia or pneumonia |
Severe Pneumonia
- ASHA:
- Pre referral dose of Oral amoxicillin + referral.
- CHO (Community Health Officer):
- Oral amoxicillin + IM Gentamicin + Hospitalization/Referral

If SAANS protocol is mentioned → Refer
If not mentioned → WHO → Oral amox for 5 days
Klebsiella Pneumonia:
- Bulging fissure sign:
- Horizontal fissure is curved.

Pneumatocele:
- Cavity filled with air.
- Staphylococci
- PCP (HIV +)
- Pneumatocele + ground glass opacity → perihilar region.

Congenital pulmonary malformations
