Difference between revisions of "Pulmonary Langerhans cell histiocytosis"
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| Prevalence = uncommon | |||
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| Prognosis = good with smoking cessation | |||
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'''Pulmonary Langerhans cell histiocytosis''' is an uncommon [[smoking|smoking-related lung disease]]. | '''Pulmonary Langerhans cell histiocytosis''' is an uncommon [[smoking|smoking-related lung disease]]. | ||
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==IHC== | ==IHC== | ||
*Langerhans cells: S100+ and CD1a+.<ref name=Ref_PPP237>{{Ref PPP|237}}</ref> | *Langerhans cells: S100 +ve and CD1a +ve.<ref name=Ref_PPP237>{{Ref PPP|237}}</ref> | ||
==See also== | ==See also== |
Revision as of 06:10, 23 December 2015
Pulmonary Langerhans cell histiocytosis | |
---|---|
Diagnosis in short | |
Site | lung - see medical lung diseases |
| |
Prevalence | uncommon |
Radiology | upper lung zones |
Prognosis | good with smoking cessation |
Pulmonary Langerhans cell histiocytosis is an uncommon smoking-related lung disease.
It is also known as eosinophilic granuloma of the lung.
General
- Associated with smoking.[1]
- Not associated with systemic diseases of Langerhans cells (AKA Hand-Schueller-Christian disease).
Subtypes:[1]
- Cellular form.
- Fibrotic form.
One form usually predominates.
Radiology
- Upper lung zones.
Microscopic
Features:[2]
- Cellular peribronchiolar nodules with:
- Langerhans cells - key feature:
- Pale staining nucleus (H&E) with nuclear infolding - "crumpled tissue paper" appearance.
- +/-Smoker's macrophages (brown pigmented airspace macrophages).
- +/-Eosinophilia (may be rare) - significantly narrow DDx.
- Chronic inflammatory cells (lymphocytes). (???)
- Langerhans cells - key feature:
Images:
IHC
- Langerhans cells: S100 +ve and CD1a +ve.[2]
See also
References
- ↑ 1.0 1.1 Leslie, Kevin O.; Wick, Mark R. (2004). Practical Pulmonary Pathology: A Diagnostic Approach (1st ed.). Churchill Livingstone. pp. 234. ISBN 978-0443066313.
- ↑ 2.0 2.1 Leslie, Kevin O.; Wick, Mark R. (2004). Practical Pulmonary Pathology: A Diagnostic Approach (1st ed.). Churchill Livingstone. pp. 237. ISBN 978-0443066313.