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 Hematol. Malignancy (histiocytosis)| CurrentStatus = reconciled
 
| InitialEditorAssigned = Elaine Nagy
}}
{{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 ==
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*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.
*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
*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
== Alternate ICD10s to consider coding instead or in addition ==


=== 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 ==


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

Latest revision as of 15:36, 4 March 2021

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


 
 
 
 

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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
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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

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