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

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See [[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]] instead.  
See [[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]] instead.  
{{Discuss |
* this dx was included in error
* existing records in CFE should be changed to [[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]] (C96) instead, and then this page can be deleted.
* emailed Pagasa to update the codes in CFE and then report back on this page. Ttenbergen 13:43, 2020 October 27 (CDT)
* sent follow-up email [[User:Ttenbergen|Ttenbergen]] 12:21, 2021 February 11 (CST)
}}


{{ICD10 dx
{{ICD10 dx
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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
=== 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 ==

Latest revision as of 15:36, 4 March 2021

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


 
 
 
 

Legacy Content

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  • Explanation: This is a legacy diagnosis, its stop date is in the past.
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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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