Langerhans cell histiocytosis: Difference between revisions
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(Created page with "== Background == * Rare inflammatory or neoplastic process that can effect a number of organs, characterized by the granulomatous inflammation involving Langerhans cells (denfritic antigen-presenting cells) * Most common under 15 years of age, but can present at any age == Clinical Manifestations == * Rash is most common feature, with general appearance similar to seborrheic dermatitis or atopic dermatitis (in children) ** Scaly papules, nodules, plaques ** Ma...") Â |
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== Background == |
== Background == |
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| − | * Rare inflammatory or neoplastic process that can effect a number of organs, characterized by the granulomatous inflammation involving Langerhans cells ( |
+ | * Rare inflammatory or neoplastic process that can effect a number of organs, characterized by the granulomatous inflammation involving Langerhans cells (dendritic antigen-presenting cells) |
* Most common under 15 years of age, but can present at any age |
* Most common under 15 years of age, but can present at any age |
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Latest revision as of 09:37, 26 October 2023
Background
- Rare inflammatory or neoplastic process that can effect a number of organs, characterized by the granulomatous inflammation involving Langerhans cells (dendritic antigen-presenting cells)
- Most common under 15 years of age, but can present at any age
Clinical Manifestations
- Rash is most common feature, with general appearance similar to seborrheic dermatitis or atopic dermatitis (in children)
- Scaly papules, nodules, plaques
- May have petechiae, bloody crusting, or indurated nodules
- Bony involvement happens in most patients (80%)
- Usually incidental
- Usually solitary
- Can involve skull, hip, pelvis, femur, or ribs
- Lung involvement is less common (20%)
- Lymphadenopathy in 30%
- Possibly hepatosplenomegaly
- Possibly infiltration of pituitary causing diabetes insipidus, with polyuria, polydipsia, and hypernatremia
