Interstitial lung disease, NOS: Difference between revisions

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{{ICD10 transition status

| OldDxArticle = Pneumonitis NYD, Other respiratory problems

| OldDxArticle = Pneumonitis NYD; Other respiratory problems

| CurrentStatus = reconciled

| InitialEditorAssigned = Lori Lovell

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== Additional Info ==

*This code includes:

**Alveolar proteinosis

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

**Idiopathic pulmonary hemosiderosis

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

**Lymphangioleiomyomatosis (LAM)

**~~Histiocytosis X~~

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

**~~Langerhans cell histiocytosis~~

**Interstitial granulomatous lymphocytic lung disease

**Follicular bronchiolitis

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

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

*[[Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis)]]

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

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

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

*[[Fibrothorax]]

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== Related CCI Codes ==

== Related Articles ==

@@ Line 1: / Line 1: @@
 {{ICD10 transition status
-| OldDxArticle = Pneumonitis NYD, Other respiratory problems
+| OldDxArticle =  Pneumonitis NYD; Other respiratory problems
 | CurrentStatus = reconciled
 | InitialEditorAssigned = Lori Lovell
@@ Line 13: / Line 13: @@
 == Additional Info ==
 *This code includes:
-**Alveolar proteinosis
+**Alveolar proteinosis, also called Primary Alveolar Proteinosis (PAP)
 **Idiopathic pulmonary hemosiderosis
 **Lipoid interstitial pneumonitis -- sometimes incorrectly called or Lipoid interstitial pneumonia
 **Lymphangioleiomyomatosis (LAM)
-**Histiocytosis X
+**To code pulmonary fibrosis post-COVID19, combine this code with [[Post COVID-19 condition]]
-**Langerhans cell histiocytosis
+**Interstitial granulomatous lymphocytic lung disease
+**Follicular bronchiolitis
 == Alternate ICD10s to consider coding instead or in addition ==
 *[[Interstitial lung disease, drug-induced (acute or chronic)]]
-*[[Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis)]]
 *[[Hypersensitivity pneumonitis (extrinsic allergic alveoliltis), NOS]]
+*[[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]]
 *[[Pulmonary emphysema or bullous disease without COPD]]
 *[[Fibrothorax]]
@@ Line 34: / Line 35: @@
 == Related CCI Codes ==
+{{Data Integrity Check List}}
 == Related Articles ==
 {{Related Articles}}
 {{ICD10 footer}}
 {{EndPlaceHolder}}