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Table 2 Etiology in UIP pattern

From: Fibrosing pneumonia – how to diagnose, and how to recognize the etiology?

  Myofibroblastic foci, cystic remodeling, timely heterogeneity LIP pattern ± hyperplasia of BALT Organizing pneumonia pattern DAD pattern Granulomas or giant cells Lymphocytes, subtypes?
IPF present no no ± in exacerbation no No
Chronic autoimmune disease present Yes/no Yes/no no Yes/no Mixed CD4/8 and CD20 population
Chronic hypersensitivity pneumonia present Yes/no peribronchial lymphocyte aggregates yes no yes Predominant CD8 population
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