download - Malaysian Thoracic Society
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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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