Fibrotic hypersensitivity pneumonitis (fHP) is a chronic, often progressive fibrosing form of hypersensitivity pneumonitis and is also often categorized as a form of interstitial lung disease. Manifestations previously categorized as chronic hypersensitivity pneumonitis now fall under this category. As with other forms of hypersensitivity pneumonitis it is caused by inhaled antigenic exposures.
Radiographic features
CT
The associated lung fibrosis can frequently demonstrate bronchocentricity 5
The collaborative American Thoracic Society (ATS), Japanese Respiratory Society (JRS), and Latin American Thoracic Association (ALAT) guidelines suggest using the three descriptors "typical", "compatible with", or "indeterminatefor" fibrotic hypersensitivity pneumonitis 3:
typical hypersensitivity pneumonitis
coarse reticulation and minimal honeycombing in a random axial distribution with no zonal predominance
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