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Respiratory System Disorders 4 Lecture 26 Pathology and Clinical Science 1 (BIOC211) Department of Bioscience Text Reference: Porth’s Pathophysiology: Concepts of Altered Health States Sheila C. Grossman & Carol Mattson Porth. Ninth Edition. Copyright © 2014 Lippincott, Williams & Wilkins Publishers, Inc. © endeavour.edu.au

Respiratory System Disorders 4 · From Porth’s Pathophysiology: Concepts of Altered Health States. (9th ed., p. 984), by Sheila C. Grossman & Carol Mattson Porth

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Respiratory System Disorders 4

Lecture 26

Pathology and Clinical

Science 1 (BIOC211)

Department of BioscienceText Reference:

Porth’s Pathophysiology: Concepts of Altered Health States

Sheila C. Grossman & Carol Mattson Porth.

Ninth Edition.

Copyright © 2014 Lippincott, Williams & Wilkins Publishers, Inc.

© endeavour.edu.au

© Endeavour College of Natural Health endeavour.edu.au 2

SESSION LEARNING

OUTCOMES o This session explains the aetiology, pathophysiology,

clinical features, investigations and management of

diseases of the respiratory system.

o It aims to understand the following respiratory infections

• Lung cancers

• Interstitial pulmonary disease

• Sarcoidosis

• Lung diseases caused by organic and inorganic dusts

• Alveolitis

• Vascular diseases

© Endeavour College of Natural Health endeavour.edu.au 3

TUMOURS OF THE BRONCHUS

AND LUNG

Introduction

• Lung cancer is the most common cancer

worldwide (1.2 million new cases in 2000 & 18%

of cancer death)

• Tobacco use is the major preventable cause

• Majority of tumours in the lung are primary

bronchial carcinoma

• The lung is also a common site of secondary

metastatic carcinoma

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PRIMARY TUMOURS

OF THE LUNGAetiology

• Cigarette smoking most common and though to be responsible for 90% of lung carcinomas

• Risk proportional to amount smoked and tar content

• Passive smoking though to be a factor in 5% of lung cancers though difficult to quantify

• Other risk factors – exposure to naturally occurring radon, atmospheric pollution and occupation dealing with some industrial products e.g. asbestos, cadmium

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BRONCHIAL CARCINOMA

Pathophysiology

o Arise from either bronchial epithelium or mucous gland

o Common cell types are squamous 35%,

adenocarcinoma 30%, small cell and large cell

o Onset of symptoms is dependent on cell types &

position

within the bronchus

o Can directly involve the pleura or by lymphatic spread

o Blood-borne metastasis occur mainly to liver, bone,

brain, adrenals and skin

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SMALL CELL CARCINOMA

http://medicalassessmentonline.com/john/CancerLungSmallCellcancer2014.jpg

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BRONCHIAL CARCINOMA

Clinical features

• Cough (dry or with sputum)

• Haemoptysis

• Bronchial obstruction

– complete or partial

– with or without infection

• Breathlessness

• Pleural pain

• Symptoms due to blood-borne metastasis

• Non-metastatic extrapulmonary manifestations

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BRONCHIAL CARCINOMA

Investigations

• Chest X ray

• CT

• Bronchoscopy and biopsy

Management

• Surgical resection

• Radiotherapy

• Chemotherapy

• Palliative

Prognosis

• Very poor (5 year survival less than 6%)

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BRONCHIAL CARCINOMA

radiology.med.sc.edu/BronchialCA.htm

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BRONCHOGENIC

CARCINOMA

http://www.meddean.luc.edu/lumen/MedEd/medicine/pulmonar/images/path4/sld37.jpg

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SECONDARY TUMOURS

OF THE LUNGo Blood-borne metastatic pulmonary

deposits from breast, kidney, uterus, ovary,

testes and thyroid

o Deposits are usually multiple and bilateral

o There are respiratory symptoms e. g.

breathlessness

o Diagnosis is made by radiological

examination

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INTERSTITIAL & INFILTRATIVE

PULMONARY DISEASESDiffuse parenchymal lung disease (DPLDs)

• Heterogeneous group of conditions associated with diffused thickening of the alveolar walls with inflammatory cells and exudates

• Include

–Acute respiratory distress syndrome

–Granulomas ( e.g. sarcoidosis )

–Alveolar haemorrhage and fibrosis

• Lung disease alone or part of systemic connective tissue disorder

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SARCOIDOSIS o Multisystem granulomatous disorder

o More commonly seen in colder parts of Northern Europe

Aetiology – uncertain

Pathology

• Granulomas mostly in mediastinal and superficial lymph nodes, lungs, liver, spleen, skin, eyes, parotid glands and phalangeal bones

Clinical features

• Asymptomatic

• Lofgren’s syndrome in young women

• Respiratory symptoms

• Skin lesions

• Lymphadenopathy

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From Davidson’s Principles & Practice of Medicine (22st ed., p. 714) by B.R. Walker,

N.R. Colledge, S. H Ralston & I.D. Penman. 2014. Edinburgh. Churchill, Livingstone

Elsevier.

Sarcoidosis

A multisystem

disease

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SARCOIDOSIS

Investigation

• Blood tests, liver function tests

• Chest X ray

• Bronchoscopy and biopsy

Management

• Majority – spontaneous remission

• NSAIDs and corticosteroids

Prognosis

• Overall mortality low 1-5%

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Sarcoidosis

http://nikon2.magnet.fsu.edu/galleries/pathology/images/sarcoidosis/sarcoidosis20x02large.jpg

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LUNG DISEASES DUE TO

ORGANIC DUSTS

o Disease results from a local immune response to animal proteins or fungal antigens in mouldyvegetable matter

o Some examples

• Farmer’s lung (mouldy hay, straw, grain)

• Bird fancier’s lung (avian excreta, feathers)

• Malt worker’s lung

• Cheese worker’s lung (mouldy cheese)

o Most commonly presented as hypersensitivity pneumonitis

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HYPERSENSITIVITY PNEUMONITIS

(EXTRINSIC ALLERGIC ALVEOLITIS)

Pathogenesis

• Inhalation of certain types of organic dusts → diffuse immune complex reactions (Type III & type IV) in the walls of alveoli and bronchioles

• Chronic forms may lead to fibrosis

Clinical features

• History of exposure

• Flu-like symptoms – headache, myalgia, malaise, fever, dry cough, breathlessness

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HYPERSENSITIVITY PNEUMONITIS

(EXTRINSIC ALLERGIC ALVEOLITIS)

Investigations

• Chest X ray

• HRCT

• Pulmonary function tests

• Blood test – presence of antibodies to offending antigen

Management

• Removal of antigen or dust masks with appropriate filters

• Steroids

• Oxygen therapy in severely hypoxic patients

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ALVEOLITIS

http://www.humpath.com/IMG/jpg/acute_alveolitis_acute_pneumonia_a.jpg

Alveolitis as seen in acute bacterial pneumonia

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LUNG DISEASES DUE TO

INORGANIC DUSTSo Specific pathological changes in the lungs due to

exposure to dusts, fumes or noxious substances

o Generally prolonged exposure to inorganic dusts leads to diffuse pulmonary fibrosis (pneumoconiosis)

o Damage is from the inflammatory and fibrotic response to the dust

o Generally a long period of exposure is required

o Exposure can lead to other lung diseases

o Need a detailed occupational case history

o Diagnose by history, radiological and pulmonary function abnormalities

o No specific treatment is available for this group of diseases

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LUNG DISEASES DUE TO

INORGANIC DUSTSCoal Workers Pneumoconiosis - Inhalation of coal dust

o Simple - does not progress after exposure is stopped

o Progressive - massive Fibrosis

• Disease is disabling, can shorten life expectancy and can progress even after exposure is stopped

• Associated with chronic bronchitis, cough and sputum

Silicosis - Inhalation of silica dust

o Clinical features similar to coal workers pneumoconiosis

Asbestosis - Inhalation & exposure to asbestos dust

o Cause laryngeal carcinoma plus pleural and lung pathologies

o Decreases lung volumes and restricts ventilation of the lungs

o Usually progresses very slowly

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COAL MINERS PNEUMOCONIOSIS

Stevens & Lowe page 209

http://img.medscapestatic.com/pi/meds/ckb/09/38609tn.jpg

http://img.wikinut.com/img/3kh89at852q2nsi_/jpeg/180x300/Coal-Miners.jpeg

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SILICOSIS

https://o.quizlet.com/5bhRnQLyjE6kdorTKl9xFA_m.png

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ASBESTOS BODIES

Stevens & Lowe page 210

http://2.bp.blogspot.com/-

_3zIIyiJjCU/TtpbfbPvLRI/AAAAAAAAAMc/KqLCZic6r1s/s1600/asbes.jpg

http://upload.wikimedia.org/wikipedia/commons/7/71/Lung_asbestos_bodies.jpg

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From Essential Pathology. (3rd ed., p. 330) by Rubin E.. 2001. Philadelphia. Lippincott,

Williams & Wilkins

INORGANIC

DISEASE

COMPARISON

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PULMONARY VASCULAR

DISEASE

Venous thromboembolism (VTE)

• Majority ( 75% )of pulmonary emboli arise from lower limb DVT

• Risk factors – surgery, pregnancy, cardiopulmonary disease, lower limb problem, malignant disease

• Pathophysiology

– Based on size of the embolus

– Acute massive, acute small or medium, chronic multiple micro emboli

– Causes blockage or blood vessels in the lungs preventing the effective exchange of gases

– Leads to hypoxia and hypercapnia

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VENOUS THROMBOEMBOLISM

(VTE)

Clinical features

• Depend on size of embolism and underlying

disease

• Range from small emboli with few or no

haemodynamic consequences to

cardiovascular collapse

• Usually chest pain, dyspnoea, haemoptysis,

fainting

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VENOUS THROMBOEMBOLISMInvestigations

• Chest X-ray

• ECG

• Arterial blood gas analysis

• Ventilation perfusion scanning

• Echocardiography

• Pulmonary angiograph

Management

• General measure – pain relief, oxygen, resuscitation

• Anticoagulants

• Thrombolytic therapy

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PULMONARY

EMBOLISM

From Porth’s Pathophysiology: Concepts of Altered Health

States. (9th ed., p. 984), by

Sheila C. Grossman & Carol Mattson Porth.

Philadelphia, U.S.A. Walters Kluwer Health - Lippincott,

Williams & Wilkins

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DISEASES OF THE PLEURA

Pleurisy

o Term for any disease that involves the

pleura and leads to pleural pain or friction

• Common in pulmonary infarction, TB or

Tumour

• Clinical features are dependent on the

nature of the disease causing the pain

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EMPYEMA

o The presence of pus in the pleural space (Thin like serous fluid or Incredibly thick)

o Generally unilateral – involving the whole or part of a lung

o Always secondary - generally to infection of the lung

o Bacterial pneumonia and TB

Pathophysiology

o The pleura becomes covered with a thick shaggy inflammatory exudate

o The pus is generally under pressure and can erupt into a bronchus if not treated

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EMPYEMA

Clinical Features

o Persistent recurrent pyrexia in a patient already diagnosed with lung infection particularly if antibiotic treatment is being given

Treatment and Management

o Dependent of the underlying cause

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EMPYEMA

http://healthmediconline.com/wp-content/uploads/2011/05/empyema.jpg

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SPONTANEOUS PNEUMOTHORAXPresence of air in the pleural space

Causes

o Rupture of a sub pleural emphysematous bulla or pleural bleb

o Rupture of a sub pleural tuberculoses focu

Pathophysiology

o Closed - No communication between the pleura and lungs with deflation

o Open - Communication between the lungs and the pleural space generally through a bronchus

o Tension / Valvular

• Communication present but small and only allows movement of air in one direction

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SPONTANEOUS PNEUMOTHORAX

Clinical Features

o Onset generally rapid, may present with infection

o Pain or tightness on the affected side of the chest

aggravated by deep breathing and dependent on the size of the pneumothorax and the type

o Breathlessness and cyanosis

o Hyper-resonance on percussion and increased vocal resonance

Treatment and Management

o Bed rest

o Infection must be countered in open pneumothorax

o Valvular pneumothorax can be extreme resulting in death within minutes though generally time for medical intervention

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PNEUMOTHORAX

From Porth’s Pathophysiology: Concepts of Altered Health

States. (9th ed., p. 966), by

Sheila C. Grossman & Carol Mattson Porth.

Philadelphia, U.S.A. Walters Kluwer Health - Lippincott,

Williams & Wilkins

© Endeavour College of Natural Health endeavour.edu.au 38

CONGENITAL DISORDERS OF

THE DIAPHRAGM

Diaphragmatic Hernias

o Defects of the diaphragm allowing herniation of the abdominal viscera. More commonly found towards the posterior aspect

Eventration of the diaphragm

o Abnormal elevation or bulging of one hemidiaphragm

o Usually asymptomatic

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ACQUIRED DISORDERS

OF THE DIAPHRAGMDiaphragmatic Paralysis

• Generally through phrenic nerve damage to one hemi-

diaphragm

Clinical Features

• Loss of ventilatory capacity (20%)

• Generally asymptomatic in a healthy individual

Causes

• Bronchial carcinoma

• Injury or disease of the cervical vertebrae including birth

injuries, surgery and aneurysms

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DEFORMITIES OF

THE CHEST WALL

Thoracic Kyphoscoliosis

Abnormalities of alignment of the dorsal spine

Causes

• Congenital abnormality

• Vertebral Disease - TB, osteoporosis, ankylosing spondylitis

• Trauma

• Neuromuscular disease - Poliomyelitis

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KYPHOSIS

https://uprightdoctor.files.wordpress.com/2011/07/kyphosis-adult-hyper.jpg

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DEFORMITIES OF

THE CHEST WALL

Clinical Manifestations (if severe)

• Restriction and distortion of the chest wall

• Misdistribution of the ventilation and blood flow to the lungs

• Can develop

– Type II respiratory failure - Pulmonary hypertension

– Right ventricular Failure - Survival beyond middle age uncommon

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Readings and ResourcesResources:

o Set Textbooks:

Colledge, N.R., Walker, B.R. & Ralston S.H. (2014). Davidson’s Principles and Practice of Medicine, (22nd ed.). Edinburgh.

Churchill Livingstone.

Grossman, S.C. & Porth, C.M. (2014). Porth’s Pathophysiology: concepts of altered health states, (9th ed.). Philadelphia,

U.S.A. Walters Kluwer Health - Lippincott, Williams & Wilkins.

o Additional textbooks:

Davies, A. & Moores, C. (2010). The respiratory system: basic science and clinical conditions, (2nd ed.). Edinburgh. Churchill,

Livingstone, Elsevier.

Field, M., Pollock, C., Harris, D. (2010). Systems of the Body: The Renal System; Basic Science and Clinical Conditions. (2nd

ed.). United Kingdom: Churchill Livingstone.

Jamison, J.R. (2006) Differential Diagnosis for Primary Care: a handbook for health care practitioners. (2nd ed.). Edinburgh.

Churchill Livingstone.

Lee, G. & Bishop, P. (2013). Microbiology and Infection Control for Health Professionals, (5th ed.). Frenchs Forest, NSW.

Pearson Education.

McCance, K.L. & Huether, S.E. (2014). Pathophysiology: the biological basis for disease in adults and children, (7th ed.). St.

Louis, MO. Elsevier.

Murphy, K. (2011). Janeway’s immunobiology, (8th ed.). New York. Garland Science.

Noble, A., Johnson, R. & Bass, P. (2010). The cardiovascular system: basic science and clinical conditions, (2nd ed.).

Edinburgh. Churchill, Livingstone, Elsevier.

Pagana, K.D. & Pagana, T.J. (2013). Mosby’s diagnostic and laboratory test reference, (11th ed.). St. Louis, MO. Elsevier.

Smith, M.E. & Morton, D.G. (2010). The digestive system: basic science and clinical conditions, (2nd ed.). Edinburgh.

Churchill, Livingstone, Elsevier.

VanMeter, K.C. & Hubert, R. (2014). Gould’s pathophysiology for health professions, (5th ed.). St. Louis, MO. Elsevier.

© Endeavour College of Natural Health endeavour.edu.au 44

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