Suppurative Lung DIsease

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    By

    Dr. Eman Arram

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    Bronchiectasis is an abnormal

    permanent dilatation of the mediumsized cartilagenous bronchi,

    accompanied by variable destruction of

    muscular and elastic components of

    the bronchial walls. It may be

    congenital or acquired. It may be focalor diffuse.

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    It is a syndrome & characterized by

    cough and expectoration that is

    usually copious and related to

    posture and time

    It includes:

    Bronchiectasis

    Lung abscess

    Empyema with bronchopleural fistula

    Infected cystic lung

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    Dilatation of medium sized

    subsegmental bronchi from about the

    4th to 9th generations and filling with

    purulent secretions or mucus plugs.

    Bronchial wall inflammation and

    destruction and replacement of the all

    components of the wall by fibrous

    tissue.

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    Pathogenesis:

    Initiating factors for bronchiectasis:

    Infection

    Bronchial obstruction

    Fibrosis

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    Site: Bilateral in 30% of patients.

    Left lower lobe > Rt lower lobe (>3 times). Left LL posterior basal segments is almost

    always affected then lingula then Rt LL thenmiddle lobe.

    The particular lobes affected may sometimesbear a relationship to underlyingpredisposition:

    Upper lobe bronchiectasis is often 2ry to TB,lung abscess or cystic fibrosis.

    Middle lobe bronchiectasis in TB.

    Central bronchiectasis in ABPA.

    Bronchiectasis due to FB aspiration is more inthe Rt LL or in post segment of UL.

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    Classification (Reids classification) Cylindrical (tubular)

    Cystic (saccular)

    Varicose

    Fusiform

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    A) Congenital and hereditary disorders: Primary ciliary dyskinesia syndromes (PCD).

    Cystic fibrosis

    Alpha1 anti-trypsin deficiency

    Tracheomalacia

    Tracheobronchomegally Intralobar bronchopulmonary sequestration

    Immunodeficiency syndromes

    Yellow nail syndrome

    Aetiology of Bronchiectasis

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    Kartagners syndrome:

    Bronchiectasis. Sinusitis or absent frontal air

    sinuses

    Situs inversus

    Youngs syndrome:

    Recurrent pulmonary infections

    predisposing to bronchiectasis

    Sinusitis

    Infertility (obstructive azospermia)

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    B) Acquired bronchiectasis:

    1- Post-infection:

    Bacterial: klebsiela pneumonia, S.

    aureus, B. pertussis.

    Mycobacteria.

    Mycoplasma.

    Viruses as infleunza, adenoviruses,

    herpes simplex, measless and HIV.

    Fungi eg histoplasmosis.

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    2- Bronchial obstruction:

    Endobronchial: FB, tumor, mucoid impaction.

    Extrabronchial compression: LN, tumor, aneurysm.

    Bronchial stenosis.

    3- Chronic obstructive pulmonary disease.

    4- Inhalation / Aspiration injury:

    Inhalation of irritants such as ammonia, NO2, smoke

    and toxic fumes.

    Heroin use. Aspiration of gastric contents.

    Recurrent aspiration pneumonias, alcoholism,

    neurologic disorders, lipoid pneumonia.

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    5- Autoimmune diseases:

    Inflammatory bowel disease. Coeliac disease.

    SLE.

    Rheumatoid arthritis. Cryptogenic fibrosing alveolitis.

    Primary biliary cirrhosis.

    Thyroiditis.

    Pernicious anemia.

    .

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    Clinical presentation of

    bronchiectasis: Chronic cough with copious amount

    of foul-smelling sputum more in the

    morning and on leaning forwards with

    characteristic winter exacerbations.

    Dyspnea.

    Chest pain.

    Haemoptysis.

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    Wheezy chest.

    Concomitant sinusitis in some cases.

    General manifestations: fever, weight

    loss, growth retardation, GIT troubles.

    Clubbing of the fingers and may be

    HPOA.

    Oedema LL.

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    Complications of bronchiectasis:

    Recurrent haemoptysis, pneumoniaand pleurisy are common.

    Lung abscess and metastatic brain

    abscess.

    Amyloidosis.

    Cor pulmonale and respiratoryfailure.

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    1) Chest radiography:

    Investigations

    Tooth past or gloved finger

    appearance.

    Tramlines appearance. Honeycoomb or soap bubble

    appearance in cystic bronchiectasis.

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    2) Bronchography:

    It was the investigation of choice.

    3) HRCT chest:

    Is now the favored investigation of

    establishing the diagnosis ofbronchiectasis.

    Cylindrical bronchiectasis appears as

    uniformly dilated airways.

    Signet ring sign: dilated bronchi appear

    as ring structures with internal diameters

    greater than those of their accompanying

    pulmonary artery branches.

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    Bronchogram showing cystic

    bronchiectasis

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    4) Fiberoptic bronchoscopy:

    Evaluation of patients with recurrenthaemoptysis.

    Perform more selective segmental

    bronchography.

    5) Sputum culture and sensitivity:

    H.influenza, S.pneumoniae, moraxella

    catarrhalis, staphyloccocus aureus,

    klebsiella pneumonia, pseudomonas

    aeruginosa, adenovirus and anaerobes.

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    6) Pulmonary function tests:

    Obstructive ventilatory defect is the

    predominant defect usually mild.

    Preoperative evaluation of patients.

    7) Other investigations: Sweat chloride test in CF.

    Serum immunoglobulins.

    ECG evidence of cor pulmonale inadvanced disease.

    CBC anaemia and leucocytosis.

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    A) Medical treatment:

    1) Postural drainage:

    Gravitational drainage of accumulated sputum in

    the bronchiectatic area facilitated by directpercussion, mechanical percussors and vibrators.

    Treatment

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    2) Antimicrobial therapy:

    Amoxycelline 250mg TDS for 2 weeks may be

    increased to 3 gm twice daily in severe cases.

    Ofloxacin 200 mg twice daily for 10-15 days.

    Clarithramycin 250 mg twice daily for 10 days.

    Tetracyclines.

    B lactam antibiotics e.g. amoxycelline

    clavulinic acid.

    Antistaph, antipseudomonal antibiotics.

    Nebulized antibiotics for pseudomonas

    aeruginosa.

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    3) Expectorants and mucolytics.

    4) Bronchodilators.

    5) Corticosteroids: when there is failure

    to obtain an adequate response to

    bronchodilators.6) Human gamma globulin: IM 25 mg/kg

    weekly or 2 weekly intervals in patients

    with immunodeficiency syndromes.7) Vaccination: by influenza and

    pneumoccocal vaccine specially in

    children.

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    B) Surgical treatment:

    Indications: The diagnosis has been confirmed with

    bilateral bronchogram or HRCT.

    Localized disease to one lung or part ofthe lung.

    Significantly disturbed patient by

    recurrent infective exacerbation orhaemoptysis despite medical treatment

    over a period of at least 12 months.

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    Good pulmonary function. No systemic causal factor.

    Patient is less than 40 years.

    Surgical maneuvers include either

    segmentectomy, lobectomy or even

    pneumonectomy.

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    C) Embolotherapy:

    Bronchial artery embolization to control

    massive or recurrent haemoptysis for

    patient not candidates for surgery.

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    Thank you forattention