Disorders of the plueral Flashcards

1
Q

Abnormal accumulation of fluid in the pleural space, which is the potential space between the visceral and parietal pleura surrounding the lungs.

A

Pleural effusions

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2
Q

Causes of fluid accumulation

A

➢ Primary (primary intra-pleural bacterial infections,
primary neoplasm of the pleura)
➢ Secondary pleural diseases (secondary complication of some underlying disease)

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3
Q

Aetiology of plueral effusions

A

➢ Increased hydrostatic pressure in visceral pleura (e.g.Congestive Heart Failure)
➢ Decreased oncotic pressure (e.g. Nephrotic Syndrome)
➢ Increased vessel permeability of visceral pleura
capillaries (Pulmonary infarction, Pneumonia)
➢ Increased intra-pleural negative pressure (e.g.
Atelectasis)
➢ Decreased lymphatic drainage (e.g. mediastinal
Carcinomatosis)

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4
Q

Types of Pleural Effusions

A

Transudates & Exudates

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5
Q

What causes transudative pleural effusions?

A

Transudates are caused by disturbances in Starling pressures, such as:
Increased hydrostatic pressure: e.g., Congestive Heart Failure
Decreased oncotic pressure: e.g., Nephrotic Syndrome

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6
Q

What is the composition of transudative pleural effusions?

A

Transudates are an ultra-filtrate of plasma, with low protein & low cellular content.

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7
Q

What causes exudative pleural effusions?

A

Exudates are caused by increased vascular permeability due to acute inflammation.

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8
Q

What is the composition of exudative pleural effusions?

A

Exudates are protein-rich and cell-rich fluid.

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9
Q

What are some examples of conditions causing exudative pleural effusions?

A

Pneumonia
Tuberculosis
Pulmonary infarction
Malignancy/metastas

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10
Q

Clinical findings of plueral effusions

A

➢ Dullness to percussion
➢ Absent breath sounds
➢ Absent vocal tactile fremitus
➢ Contralateral shift of the mediastinum

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11
Q

Imaging studies of plueral effusions

A

➢ Blunting of the costo-phrenic angle
➢ Obscuration of the diaphragm

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12
Q

Non-inflammatory collection of serous fluid
within the pleural cavities

A

Hydrothorax

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13
Q

Causes of hyrdothorax

A

➢ Cardiac failure (Hydrothorax accompanied by
pulmonary congestion and oedema)
➢ Systemic diseases associated with generalised
oedema (e.g. Renal Failure, Cirrhosis of the liver)

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14
Q

Microscopic pic of hydroothorax

A

Clear & straw coloured fluid

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15
Q

Cause of Haemothorax

A

Complication of a ruptured aortic aneurysm
or vascular trauma or post-operative occurrence

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15
Q

Escape of blood into the pleural cavity

A

Haemothorax

16
Q

Macroscopic features of Haemothorax

A

Large clots of blood within the pleural spaces

17
Q

Cause of Pseudo-Chylothorax

A

Rheumatoid arthritis, other collagen vascular diseases, Tbc.

18
Q

What are the macroscopic features of pseudochylothorax?

A

Cloudy, opalescent (sparkling) fluid

19
Q

What is the lipid profile in pseudochylothorax?

A

Rich in cholesterol
Normal triglyceride levels
No chylomicrons

20
Q

What type of cells may be present in pseudochylothorax?

A

Lipid-laden macrophages.

21
Q

Chronic pleural effusion linked to inflammation, results in the

A

Breakdown of necrotic debris & accumulation of cholesterol

22
Q

Rare condition that results from thoracic
duct damage, with chyle leakage from the lymphatic
system into the pleural space

A

chylothorax

23
Q

What is empyema?

A

A purulent pleural exudate caused by bacterial or fungal seeding of the pleural space.

24
Q

What are the causes of empyema?

A

Contiguous spread from intrapulmonary infection (most common).
Lymphatic or hematogenous spread from distant sites.
Extension from infections below the diaphragm (e.g., liver abscess).

25
Q

Describe the macroscopic & microscopic appearance of empyema.

A

Macroscopic: Loculated, yellow-green creamy pus.
Microscopic: Masses of neutrophils with other leukocytes.

26
Q

What are possible outcomes of empyema?

A

Resolution (less common).
Organization of exudate → Dense fibrous adhesions → Obliteration of pleural space.
Envelopment of lungs → Restricted pulmonary expansion.

27
Q

What are the types of inflammatory pleural effusions?

A

Serous.
Sero-fibrinous.
Fibrinous (severe exudative reaction, later stage).

28
Q

What are some causes of serous or sero-fibrinous pleuritis?

A

Lung inflammatory diseases: Tuberculosis, pneumonia, lung abscess, bronchiectasis.
Autoimmune diseases: Rheumatoid arthritis, lupus.
Uremia or systemic infections.
Radiation therapy for lung/mediastinal tumors.

29
Q

What causes true hemorrhagic pleuritis?

A

Hemorrhagic diathesis.
Rickettsial diseases.
Neoplastic involvement of the pleural cavity.

30
Q

What are some DD of pleuritis?

A

Haemorrhagic Pneumothorax

31
Q

What does true hemorrhagic pleuritis manifest by?

A

Sanguineous inflammatory exudates.

32
Q

What is chyle composed of?

A

Cholesterol, triglycerides, chylomicrons, fat-soluble vitamins, and lymph.

33
Q

What are chylomicrons, and how are they transported?

A

Chylomicrons are molecular complexes of proteins and lipids synthesized in the jejunum and transported via the thoracic duct to circulation.

34
Q

What does lymph contain?

A

Immunoglobulins, enzymes, digestive products, and lymphocytes.

35
Q

Describe the pathogenesis of chylothorax.

A

Leakage of thoracic duct → Chyloma (fluid below pleura).
Chyloma bursts through pleura → Chyle accumulates:
In pleural space → Chylothorax.
In mediastinum → Chylomediastinum.
In pericardium → Chylopericardium.

36
Q

What are the clinical features of chylothorax?

A

Rapid loss → Hypovolemia, respiratory difficulty.
Loss of protein, fats, & vitamins → Malnutrition.
Loss of electrolytes → Hyponatremia, hypocalcemia.
Loss of Igs & lymphocytes → Immunosuppression.
Dyspnea, chest pain, and cough.

37
Q

What are the most common localizations of chylothorax?

A

Right-sided effusion: 50% (duct damage below the 5th thoracic vertebra).
Left-sided effusion: 33.3% (duct damage above the 5th thoracic vertebra).
Bilateral effusion: 16.66%.

38
Q

What investigations are used for chylothorax?

A

Thoracentesis & laboratory analysis.
CT of abdomen & thorax: Detect tumor or lymphadenopathy.
Lymphangiography: Locate site of leakage/blockage.
Cytological analysis with Sudan III stain: Detect chylomicrons.