Langerhans' cell histiocytosis (Histiocytosis X, Eosinophilic granulomatosis): Difference between revisions
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* emailed Pagasa to update the codes in CFE and then report back on this page. Ttenbergen 13:43, 2020 October 27 (CDT) | * 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) | * sent follow-up email [[User:Ttenbergen|Ttenbergen]] 12:21, 2021 February 11 (CST) | ||
* This is done. | |||
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Revision as of 13:51, 16 February 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.
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
Alternate ICD10s to consider coding instead or in addition
Candidate Combined ICD10 codes
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Related Articles
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