Usual Interstitial Pneumonia

Preferred Label : Usual Interstitial Pneumonia;

NCIt synonyms : UIP;

NCIt definition : Interstitial pneumonia characterized by the presence of fibrosis in the interstitial lung tissue. The pathologic diagnosis is based on the identification of fibrotic lesions at different stages of development within a lung biopsy specimen. Typically there are foci of normal lung parenchyma alternating with interstitial inflammation and honeycombing. The term usual interstitial pneumonia sometimes is used interchangeably with idiopathic interstitial fibrosis. The two terms are not entirely synonymous. Usual interstitial pneumonia may be associated with other conditions such as connective tissue disorders and asbestosis. The diagnosis of idiopathic interstitial fibrosis requires the exclusion of such conditions. Patients with usual interstitial pneumonia present with progressive dyspnea, cough, and restrictive pulmonary function abnormalities. The prognosis is usually poor.;

NCI Metathesaurus CUI : CL497284;

Détails

Origin ID

C35715;

UMLS CUI

C4721509;

Automatic exact mappings (from CISMeF team)
- Idiopathic fibrosing alveolitis, chronic form (disorder) [Inactive SNOMED CT concept]
- Idiopathic pulmonary fibrosis [ORDO Disease]
- Idiopathic pulmonary fibrosis (disorder) [SNOMED CT concept]
- Interstitial lung disease 2 [OMIM Phenotype]
- Intracranial pressure (observable entity) [SNOMED CT concept]
- Peak (qualifier value) [SNOMED CT concept]
- TDM Peak [LOINC Challenge]
- Usual Interstitial Pneumonia [MeSH concept]
- Usual interstitial pneumonia [HPO term]
- Uterus [LOINC System]
- Uterus [LOINC System]
- idiopathic pulmonary fibrosis [MeSH Descriptor]
- idiopathic pulmonary fibrosis [MeSH concept]
- intracranial pressure [MeSH Descriptor]
- usual interstitial pneumonia [Radlex concept]
- uterus [MeSH Descriptor]
Has associated anatomic sites
- Lung [NCIt concept]
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cryptogenic fibrosing alveolitis [MedDRA LLT]
- Familial idiopathic pulmonary fibrosis (disorder) [SNOMED CT concept]
- Idiopathic fibrosing alveolitis, chronic form (disorder) [Inactive SNOMED CT concept]
- Idiopathic pulmonary fibrosis [MedDRA Preferred Term]
- Idiopathic pulmonary fibrosis [ORDO Disease]
- Idiopathic pulmonary fibrosis [ICD-9 code]
- Interstitial lung disease 2 [OMIM Phenotype]
- Usual interstitial pneumonia [HPO term]
- idiopathic pulmonary fibrosis [DO Concept]
- idiopathic pulmonary fibrosis [MeSH concept]
- idiopathic pulmonary fibrosis [MeSH Descriptor]
disease_has_primary_anatomic_site
- Lung [NCIt concept]
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients