Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis): Difference between revisions

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{{ICD10 transition status
See [[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]] instead.
| OldDxArticle =Other Problems| CurrentStatus = freshly automatically generated article
 
| InitialEditorAssigned = Elaine Nagy
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{{ICD10 dx
{{ICD10 dx
| MinimumCombinedCodes =
|ICD10 Code=D76.0
| ICD10 Code=D76.0
|StopDate=2020/10/27
| BugRequired=  
}}
}}
{{ICD10 category|Heme/immunology}}


== Additional Info ==
== Additional Info ==
*Langerhans' cells are white blood cells in the immune system that normally play an important role in protecting the body against viruses, bacteria and other invaders. They are found in the skin, lymph nodes, spleen, bone marrow and lungs.
*Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes. Clinically, its manifestations range from isolated bone lesions to multisystem disease.
*Eosinophilic granuloma, also known as pulmonary histiocytosis X (PHX) or pulmonary Langerhans cell histiocytosis X (PLCH), is an uncommon interstitial lung disease that is epidemiologically related to tobacco smoking


=== Legacy ===
* this dx was included in error
* existing records in CFE have been changed to [[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]] (C96) instead


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


== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==
(put links to likely candidates coded with this one, eg. a cause for a trauma.)


== Related CCI Codes ==
== Related CCI Codes ==
{{Data Integrity Check List}}


== Related Articles ==
== Related Articles ==
{{Related Articles}}
{{Related Articles}}


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{{ICD10 footer}}
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Latest revision as of 15:36, 4 March 2021

See Malignancy (clonal disorder) of blood or lymphoid tissue, NOS instead.


 
 
 
 

Legacy Content

This page contains Legacy Content.
  • Explanation: This is a legacy diagnosis, its stop date is in the past.
  • Successor: No successor was entered

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ICD10 Diagnosis
Dx: Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis)
ICD10 code: D76.0
Pre-ICD10 counterpart: none assigned
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date: 2020/10/27
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2020/10/27
    • D76.0
  • Cargo


  • Categories

Additional Info

  • Langerhans' cells are white blood cells in the immune system that normally play an important role in protecting the body against viruses, bacteria and other invaders. They are found in the skin, lymph nodes, spleen, bone marrow and lungs.
  • Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes. Clinically, its manifestations range from isolated bone lesions to multisystem disease.
  • Eosinophilic granuloma, also known as pulmonary histiocytosis X (PHX) or pulmonary Langerhans cell histiocytosis X (PLCH), is an uncommon interstitial lung disease that is epidemiologically related to tobacco smoking

Legacy

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Data Integrity Checks (automatic list)

none found

Related Articles

Related articles:


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