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Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b).

Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b).

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The aim of this procedure is to recognize observations classical of the UIP pattern, and<br />

to differentiate them from the less particular patterns present in other idiopathic interstitial<br />

pneumonias. The radiological reading should employ descriptive terminology based on the<br />

radiological–pathological correlation to prevent descriptive and conceptual issues, as<br />

suggested by the Fleischner Society (Hansell et al., 2008).<br />

It was determined by the official 2011 ATS/ERS/JRS/ALAT consensus (Raghu et al.,<br />

2011) that in HRCT, the conclusive diagnosis of UIP is based on the recognition of four<br />

“classical” observations: (1) lung collaboration should have subpleural and basal<br />

predominance, (2) existence of evident reticulation, (3) presence of honeycombing<br />

with/without traction bronchiectasis/bronchiolectasis and (4) describe the deprivation of<br />

observations contemplated to exclude a UIP pattern.<br />

The occurrence of ground glass opacities should be nonexistent or least.<br />

Honeycombing, created by groups of thin-walled cysts, subpleural with a diameter between 3<br />

and 10 mm, is a crucial observation for precisely diagnosing the UIP pattern. The diagnosis<br />

of a possible UIP pattern by HRCT in the absence of noticeable honeycombing; in such cases,<br />

the conclusive diagnosis of UIP should be done by biopsy. Lung biopsy can be ignored only<br />

when the HRCT exhibits a definitive pattern, classical of UIP. The positive prognostic value<br />

of HRCT in the diagnosis of UIP is 90%–100%. A UIP pattern can also be recognized in<br />

asbestosis, chronic hypersensitivity pneumonitis and few connective tissue diseases (Churg et<br />

al., 2006). HRCT also authorizes the existence of related comorbidities (pulmonary<br />

hypertension, emphysema, lung cancer), which may describe the clinical expansion of the<br />

disease, to be evaluated. Apart from idiopathic interstitial pneumonias, other diffuse lung<br />

diseases can also be determined by HRCT. It is suggested by the 2011 official<br />

ATS/ERS/JRS/ALAT consensus that the diagnosis of idiopathic interstitial pneumonias can<br />

be based on the consensus between the clinician, radiologist and pathologist (Raghu et al.,<br />

2011).<br />

2.2.8.4 Histopathological Pattern<br />

The surgical lung biopsy is done as the conclusive diagnosis in the case if the HRCT<br />

does not manifest a conclusive design of typical UIP. The sample for biopsy are acquired<br />

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