“…LIP LIP, also described as pulmonary lymphoid hyperplasia (PLH), is a lymphoroliferative disorder characterized by a diffuse interstitial infiltrate of polyclonal lymphocytes and plasma cells in addition to pulmonary lymphoid hyperplasia [19]. LIP is part of the diffuse infiltrative lymphocytosis syndrome (DILS), where there is infiltration of CD8 T-lymphocytes into the lungs, parotid glands, gastrointestinal tract and skin, and only occurs in those expressing the HLA DR5 alleles [12]. The cause is unknown, however it is thought to represent a direct ''hyperimmune'' lung response to the presence of either HIV or Epstein-Barr virus (EBV) and appears to be associated with a slower rate of disease progression [13,20].…”