Introduction to interstitial lung diseases
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Introduction to interstitial lung diseases. By/ Mahmoud essam el dien. Interstitial lung disease, or diffuse parenchymal lung disease.

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Introduction to interstitial lung diseases

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Introduction to interstitial lung diseases

Introduction to interstitial lung diseases

By/ Mahmoud essam el dien


Interstitial lung disease or diffuse parenchymal lung disease

Interstitial lung disease, or diffuse parenchymal lung disease

The interstitial lung diseases (ILDs) represent a large number of conditions that involve the parenchyma of the lung—the alveoli, the alveolar epithelium, the capillary

endothelium, and the

spaces between these

structures, as well as the

perivascular and lymphatic

tissues.


Introduction to interstitial lung diseases

The term "interstitial" is misleading since the pathologic process usually begins with injury to the alveolar epithelial or capillary endothelial cells

This heterogeneous group of disorders is classified together because of similar clinical, physiologic, or pathologic manifestations.


Classification

classification


Classification1

classification

One useful approach to classification is to separate the ILDs into two groups based on the major underlying histopathology:

(1) Those with a predominantly granulomatous reaction in interstitial or vascular areas

(2) Those associated with predominant inflammation and fibrosis.


Granulomatous lung disease

GRANULOMATOUS LUNG DISEASE

This process is characterized by an accumulation

of T lymphocytes, macrophages, and epithelioid cells organized into discrete structures (granulomas) in the lung parenchyma.

The granulomatous lesions can progress to fibrosis. Many patients with granulomatous lung disease remain free of severe impairment of lung function, or, when symptomatic, they improve after treatment.


Inflammation and fibrosis

INFLAMMATION AND FIBROSIS

The initial insult is an injury to the epithelial surface causing inflammation in the air spaces and alveolar walls.

If the disease becomes chronic, inflammation spreads to adjacent portions of the interstitium and vasculature and eventually causes interstitial fibrosis.

.


Cont d

cont’d

The development of irreversible scarring (fibrosis) of alveolar walls, airways, or vasculature is the most feared outcome in all of these conditions because it is often progressive and leads to significant derangement of ventilatory function and gas exchange


Risk groups

Risk groups

Age


Introduction to interstitial lung diseases

Gender

Smoking history

Duration of illness

Prior medication use

Environmental exposures


Clinical presentation

CLINICAL PRESENTATION

— Patients with ILD commonly come to clinical attention in one of the following ways:

  • With symptoms of progressive breathlessness with dyspnea or a persistent nonproductive cough.

  • With an abnormal chest radiograph.

  • With pulmonary symptoms associated with another disease, such as a connective tissue disease With lung function abnormalities.


Laboratory studies

LABORATORY STUDIES

Serologic studies should be obtained if clinically indicated by :

features suggestive of a connective tissue disease (antinuclear antibodies, rheumatoid factor),

environmental exposure or systemic vasculitis (antineutrophil cytoplasmic antibodies, anti-glomerular basement membrane antibody).


Introduction to interstitial lung diseases

Chest radiography--- normal in as many as 10 percent of patients with some forms of ILD.

Computed tomography--- increasingly important method for the evaluation of diffuse pulmonary parenchymal disease.

Serum markers--- including surfactant protein A and B (SP-A, SP-B).


Introduction to interstitial lung diseases

Pulmonary function testing --- Complete lung function testing (spirometry, lung volumes, diffusing capacity) should be obtained.

Measurement of lung function is helpful in assessing the severity of lung involvement in patients with ILD.


Introduction to interstitial lung diseases

  • Three diagnostic techniques are in common use: bronchoalveolarlavage, transbronchial biopsy, and surgical lung biopsy.

  • Bronchoalveolarlavagemay provide a specific diagnosis in cases of infection, particularly with mycobacteria, or when cytologic examination reveals the presence of malignant cells.

  • The findings may be suggestive but not diagnostic.


Introduction to interstitial lung diseases

Transbronchial biopsy is easily performed. The risks of pneumothorax and hemorrhage are low. However, the tissue specimens recovered are small, sampling error is common.

Transbronchial biopsy can make a definitive diagnosis of sarcoidosis, lymphangitic spread of carcinoma.

Transbronchial biopsy cannot establish a specific diagnosis of idiopathic interstitial pneumonia.


Surgical lung biopsy

Surgical lung biopsy

Indications for performing a lung biopsy include the following :

To assess disease activity.

To exclude neoplastic and infectious processes that occasionally mimic chronic, progressive interstitial disease.

To establish a definitive diagnosis and predict prognosis before proceeding with therapies which may have serious side effects


Introduction to interstitial lung diseases

Thank you


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