Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis)

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Revision as of 13:21, 2021 February 11 by Ttenbergen (talk | contribs)
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See Malignancy (clonal disorder) of blood or lymphoid tissue, NOS instead.

  • 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 Ttenbergen 12:21, 2021 February 11 (CST)
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This page contains Legacy Content.
  • 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.

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    • 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

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