Interstitial lung disease, NOS: Difference between revisions

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{{ICD10 transition status

| OldDxArticle =~~Pneumonia~~| CurrentStatus = ~~freshly automatically generated article~~

| OldDxArticle = Pneumonitis NYD; Other respiratory problems

| CurrentStatus = reconciled

| InitialEditorAssigned = Lori Lovell

}}

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== Additional Info ==

~~incl alveolar~~ proteinosis, ~~idiopathic~~ pulmonary hemosiderosis~~, lipoid~~ interstitial pneumonitis, ~~lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}~~

*This code includes:

**Alveolar proteinosis, also called Primary Alveolar Proteinosis (PAP)

**Idiopathic pulmonary hemosiderosis

**Lipoid interstitial pneumonitis -- sometimes incorrectly called or Lipoid interstitial pneumonia

**Lymphangioleiomyomatosis (LAM)

**To code pulmonary fibrosis post-COVID19, combine this code with [[Post COVID-19 condition]]

**Interstitial granulomatous lymphocytic lung disease

**Follicular bronchiolitis

== Alternate ICD10s to consider coding instead or in addition ==

(~~turn these into links to the actual diagnosis articles if possible. For some that might make no sense.~~)

*[[Interstitial lung disease, drug-induced (acute or chronic)]]

~~{sc:IPF~~, ~~UIP, DIP, NSIP, AIP~~, BOOP, COP~~, eosinophilic}~~

*[[Hypersensitivity pneumonitis (extrinsic allergic alveoliltis), NOS]]

*[[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]]

*[[Pulmonary emphysema or bullous disease without COPD]]

*[[Fibrothorax]]

*[[Idiopathic interstitial pulmonary fibrosis]]

*[[Bronchiolitis obliterans organizing pneumonia (BOOP, cryptogenic organizing pneumonia (COP))]]

== Candidate [[Combined ICD10 codes]] ==

~~(put links to likely candidates coded with this one, eg. a cause for a trauma.)~~

== Related CCI Codes ==

== Related Articles ==

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 {{ICD10 transition status
-| OldDxArticle =Pneumonia| CurrentStatus = freshly automatically generated article
+| OldDxArticle =  Pneumonitis NYD; Other respiratory problems
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Lori Lovell
 }}
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 }}
-{{ICD10 category|Infectious disease}}{{ICD10 category|Respiratory}}
+{{ICD10 category|Infectious disease}}{{ICD10 category|Potential infection}}{{ICD10 category|Respiratory}}
 == Additional Info ==
-incl alveolar proteinosis, idiopathic pulmonary hemosiderosis, lipoid interstitial pneumonitis, lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
+*This code includes:
+**Alveolar proteinosis, also called Primary Alveolar Proteinosis (PAP)
+**Idiopathic pulmonary hemosiderosis
+**Lipoid interstitial pneumonitis -- sometimes incorrectly called or Lipoid interstitial pneumonia
+**Lymphangioleiomyomatosis (LAM)
+**To code pulmonary fibrosis post-COVID19, combine this code with [[Post COVID-19 condition]]
+**Interstitial granulomatous lymphocytic lung disease
+**Follicular bronchiolitis
 == Alternate ICD10s to consider coding instead or in addition ==
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+*[[Interstitial lung disease, drug-induced (acute or chronic)]]
-{sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
+*[[Hypersensitivity pneumonitis (extrinsic allergic alveoliltis), NOS]]
+*[[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]]
+*[[Pulmonary emphysema or bullous disease without COPD]]
+*[[Fibrothorax]]
+*[[Idiopathic interstitial pulmonary fibrosis]]
+*[[Bronchiolitis obliterans organizing pneumonia (BOOP, cryptogenic organizing pneumonia (COP))]]
 == Candidate [[Combined ICD10 codes]] ==
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
+{{ICD10 Guideline Infection}}
-== Related  CCI Codes ==
+== Related CCI Codes ==
+{{Data Integrity Check List}}
 == Related Articles ==
 {{Related Articles}}
 {{ICD10 footer}}
 {{EndPlaceHolder}}