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Annual Congress of <strong>Malaysian</strong> <strong>Thoracic</strong> <strong>Society</strong><br />

Symposium 2B<br />

Interstitial Lung Diseases<br />

Critical analysis of the therapeutic options of<br />

idiopathic pulmonary fibrosis<br />

Low Su Ying<br />

Singapore<br />

A diagnosis of idiopathic pulmonary fibrosis (IPF) portends the worst prognosis of all diffuse parenchymal lung<br />

diseases and has had dismal response to any medical intervention thus far. The last decade has seen a flurry<br />

of publications analyzing the usefulness of different novel therapeutic agents in the hope of finding the holy<br />

grail for the treatment of IPF. In the midst of this exciting time, I have been tasked to give a critical review of<br />

the current evidence-based management of IPF.<br />

Whilst we appear to have made small steps in the right direction, many more additional clinical trials of new<br />

therapeutic modalities for IPF are desperately needed which must be done via multicentre collaborations.<br />

The treatment of IPF may eventually require combination therapies targeting different pathways involved in<br />

fibroproliferation. Finally, whilst improved survival is an important endpoint, there is a need to consider other<br />

clinically significant and meaningful endpoints as we embark on future therapeutic trials.<br />

Symposium 2B<br />

Interstitial Lung Diseases<br />

Interpreting Histopathologic Examination (HPE) Findings of<br />

Diffuse Parenchymal Lung Disease: A Note of Caution!<br />

Nor Salmah Bakar<br />

Malaysia<br />

Diffuse parenchymal lung disease (DPLD) which is also known as interstitial lung disease (ILD), comprises of<br />

various clinicopathologic entities. This includes ILD with no known etiology and ILD with known associated<br />

clinical conditions or specific etiologic agent/s. Example of ILD with no known etiology is idiopathic pulmonary<br />

fibrosis (IPF) while connective tissue diseases are among known clinical conditions that associate with ILD.<br />

Inconsistencies in the classification of ILD could cause misunderstanding to both clinicians and pathologists.<br />

Adding to this confusion, there are varieties in terminology used in ILD. In the past decade, there have been<br />

major changes with regards to the ILD, particularly in disease classification and diagnostic processes. There<br />

are also evolving concept of pathogenesis and management of certain entities in ILD. Understanding the<br />

concept evolution of ILD, along with keeping up to date with the improved classification and diagnostic<br />

processes in ILD are important for accurate interpretation of HPE report. Examples of ILD cases will be<br />

discussed to illustrate important areas when interpreting HPE findings of ILD.<br />

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