Terminology Service for NFDI4Health
Lymphocytic Interstitial Pneumonia
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http://purl.obolibrary.org/obo/NCIT_C27558
Interstitial pneumonia characterized by the presence of bibasilar pulmonary interstitial infiltrates composed of lymphocytes and plasma cells. It may be associated with autoimmune and lymphoproliferative disorders. Signs and symptoms include fever, cough, and dyspnea. Symptomatic patients may require immunosuppressive treatment. [ ]
Term info
Label
Lymphocytic Interstitial Pneumonia
Synonyms
- Diffuse Hyperplasia of Bronchus-Associated Lymphoid Tissue
- LIP
- Lymphocytic Interstitial Pneumonia
- Lymphocytic Interstitial Pneumonitis
- Lymphocytic interst. pneumonitis
- Lymphocytic interstitial pneumonitis
Subsets
NCIT_C103081, NCIT_C102905
Contributing Source
CTEP
Legacy Concept Name
Lymphocytic_Interstitial_Pneumonitis
Preferred Name
Lymphocytic Interstitial Pneumonia
Semantic Type
Disease or Syndrome
UMLS CUI
C0264511
code
C27558
Term relations
Subclass of:
- Idiopathic Interstitial Pneumonia
- Disease_May_Have_Finding some Hypergammaglobulinemia
- Disease_Has_Finding some Lymphocytic Infiltrate and Disease_Has_Finding some Diffuse Cellular Infiltrate and Disease_May_Have_Finding some Lymphoplasmacytic Infiltrate and Disease_May_Have_Finding some Reactive Germinal Centers Present and Disease_Excludes_Finding some Lymphoepithelial Lesion and Disease_Excludes_Finding some Peribronchial and Lobular Septal Involvement Only
- Disease_Has_Abnormal_Cell some Reactive Lymphocyte
- Disease_May_Have_Finding some Hypogammaglobulinemia
- Disease_Has_Associated_Anatomic_Site some Lung
- Disease_Has_Normal_Tissue_Origin some Bronchus-Associated Lymphoid Tissue
- Disease_May_Have_Associated_Disease some Sjogren Syndrome
- Disease_Excludes_Molecular_Abnormality some Clonal Antigen Receptor Gene Rearrangement
- Disease_Has_Normal_Cell_Origin some Mature Lymphocyte
- Disease_May_Have_Associated_Disease some Acquired Immunodeficiency Syndrome