Difference between revisions of "Lymphocytic interstitial pneumonia"

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{{ Infobox diagnosis
| Name      = {{PAGENAME}}
| Image      =
| Width      =
| Caption    =
| Synonyms  =
| Micro      = small mature lymphocytes in the interstitium of the lung, plasma cells, +/-lymphoid follicles
| Subtypes  =
| LMDDx      = [[lymphoma]], follicular bronchitis/bronchiolitis, nodular lymphoid hyperplasia
| Stains    =
| IHC        =
| EM        =
| Molecular  =
| IF        =
| Gross      =
| Grossing  =
| Staging    =
| Site      = [[lung]] - see ''[[diffuse lung diseases]]''
| Assdx      = autoimmune disorders ([[rheumatoid arthritis]], [[pernicious anemia]], [[Sjoegren syndrome]]), viral infections ([[HIV]], [[EBV]], human T-cell leukemia virus (HTLV) type 1)
| Syndromes  =
| Clinicalhx = dependent on underlying cause - see ''associated diagnoses''
| Signs      =
| Symptoms  =
| Prevalence = rare
| Bloodwork  =
| Rads      = basilar predominance, increased interstitial markings
| Endoscopy  =
| Prognosis  =
| Other      =
| ClinDDx    =
| Tx        =
}}
'''Lymphocytic interstitial pneumonia''' (abbreviated '''LIP'''), also known as '''lymphoid interstitial pneumonia''' and '''lymphocytic interstitial pneumonitis''', is an uncommon [[diffuse lung disease]].
'''Lymphocytic interstitial pneumonia''' (abbreviated '''LIP'''), also known as '''lymphoid interstitial pneumonia''' and '''lymphocytic interstitial pneumonitis''', is an uncommon [[diffuse lung disease]].


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