non-specific interstitial pneumonitis (NSIP)
Non-specific interstitial pneumonia (NSIP) is the second most common morphological and pathological pattern of interstitial lung diseases. NSIP has two main subtypes:
- fibrotic type: most common, having a more dismal outcome
- cellular type: less common, but carries a much better prognosis due to a very good response to the treatments
On imaging, the most common features are relatively symmetric and bilateral ground-glass opacities with associated fine reticulations and pulmonary volume loss resulting in traction bronchiectasis. Immediate subpleural sparing, when present is considered very specific for NSIP.
Non-specific interstitial pneumonia typically tends to present in middle-aged adults, 40-50 years of age . It may be common in Caucasian-European populations . Overall prevalence is higher in women due to high association with collagen vascular diseases, but the prevalence of idiopathic NSIP is similar in both genders.
Primarily idiopathic but the morphological pattern can be seen in association with a number of conditions:
- connective tissue disorders
- other autoimmune diseases
- drug-induced lung disease: especially chemotherapy agents
- hypersensitivity lung disease
- slowly healing diffuse alveolar damage (DAD)
- relapsing organizing pneumonia
- occupational exposure
- immunodeficiency (mainly HIV infection)
- graft versus host disease (GVHD)
- immunoglobulin G4 (IgG4)-related sclerosing disease, with or without overlap features with Rosai-Dorfman disease
- multicentric Castleman disease
- myelodysplastic syndrome
If there is no underlying cause, it is termed idiopathic NSIP; which is now considered a distinct entity.
Smoking is not associated, and it is not a protective factor either.
The symptoms of non-specific interstitial pneumonia are - by definition - non-specific and include insidious onset of dyspnea and dry cough with a restrictive pattern of decreased lung function and reduced gas exchange capacity.
Temporal and spatial homogeneity in a specimen is an essential feature. Historically non-specific interstitial pneumonia was divided into three groups; however, due to similar outcomes, groups II and III (mixed cellular and fibrotic and mostly fibrotic, respectively) are now both classified as fibrotic type:
- fibrotic non-specific interstitial pneumonia: more common, interstitial thickening is due to uniform dense or loose fibrosis and mild chronic inflammation; despite fibrotic changes, lung structures still preserved
- cellular non-specific interstitial pneumonia: less common; interstitial thickening is mainly due to infiltration of inflammatory cells and type II pneumocyte hyperplasia. Lung architecture is preserved
Important negative histological findings are the absence of acute lung injury including hyaline membranes, granulomas, organisms or viral inclusions, dominant airways disease or organizing pneumonia, eosinophils and coarse fibrosis.
A chest radiograph can be normal in the early stages. There may be ill-defined or ground glass opacities with lower lobe distribution or consolidation in a patchy, reticulonodular or mixed pattern. A bilateral pulmonary infiltrative pattern with volume loss of lower lobes may be seen in those with advanced disease.
Imaging features can overlap between cellular and fibrotic types as well as usual interstitial pneumonitis (UIP) in as high as 30% of patients. Also, temporal changes in the pattern of HRCT findings in subsequent studies shown in as high as 28% of cases resulted in the change of provisional diagnosis from NSIP to UIP.
Involvement tends to be subpleural and generally symmetrical with an apicobasilar gradient. Solely or predominantly upper lobe involvement or purely unilateral disease makes the diagnosis of NSIP less likely.
Common manifestations include:
- ground-glass opacities
- tends to be a dominant feature: can be symmetrically or diffusely distributed in all zones or display a basal predominance
- immediate subpleural sparing - a relatively specific sign
- mostly bilateral and symmetrical (~86% ) but can be bilateral and asymmetrical in (10%) and rarely unilateral (3%)
- mostly subpleural in distribution (~68%) but can be random (21%), diffuse (8%), and rarely central in distribution (3%)
- reticular opacities and irregular linear opacities (sometimes - minor subpleural reticulation) mainly with fibrotic NSIP
- thickening of bronchovascular bundles: with fibrotic NSIP
- traction bronchiectasis: associated with fibrotic NSIP
- lung volume loss: particularly lower lobes
- in advanced disease
The presence of the following features, although they can be seen in NSIP, should make us think about other differentials:
Treatment and prognosis
In general, non-specific interstitial pneumonia (NSIP) carries a much more favorable prognosis than a UIP-type pattern with 90% 5-year survival rate for cellular and ~60% (range 45-90%) 5-year survival in the fibrotic subtype. Cellular NSIP shows an even better response to corticosteroids and carries a substantially better prognosis than the fibrotic type. Correct and early diagnosis has a significant impact on patients' outcome because NSIP usually responds well to the corticosteroid therapy or cessation of inciting causes like drugs or organic allergens . Mycophenolate mofetil (MMF) has also shown to improve lung function .
History and etymology
It is thought to have been initially described by Katzenstein and Fiorelli in 1994 .
The key differential is a usual interstitial pneumonitis (UIP) pattern, with which there can be some overlap in imaging features . The features which favor the diagnosis of NSIP over UIP are symmetrical bilateral ground-glass opacities with fine reticulations and sparing of the immediate subpleural space. The presence of macroscopic honeycombing is almost diagnostic for UIP.
- it is important to carefully scrutinise the images, looking for findings such as joint or bony changes, esophageal dilatation, pleural and pericardial effusion, etc., as it has been mentioned earlier NSIP pattern is also associated with many other conditions