Difference between revisions of "Medical lung diseases"

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fix dup. eosinophilic granuloma, pulmonary langerhans histiocytosis
(fix dup. eosinophilic granuloma, pulmonary langerhans histiocytosis)
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Image: [http://www.scielo.br/img/revistas/jbpneu/v34n2/en_a02fig01.jpg LIP (scielo.br)].
Image: [http://www.scielo.br/img/revistas/jbpneu/v34n2/en_a02fig01.jpg LIP (scielo.br)].
==Pulmonary Langerhans cell histiocytosis==
===General===
*Assoc. with smoking.<ref name=ppp234>PPP P.234.</ref>
*Not assoc. with systemic diseases of Langerhans cells (AKA Hand-Schueller-Christian disease).
Subtypes:<ref name=ppp234/>
*Cellular form.
*Fibrotic form.
One form usually predominates.
===Histology===
Features:<ref>PPP P.237.</ref>
*Langerhans cells:
**Pale staining nucleus (H&E) with nuclear infolding - "crumpled tissue paper" appearance.
*+/-Smoker's macrophages.
*+/-Eosinophilia.
===IHC===
*Langerhans cells: S100+ and CD1a+.<ref>PPP P.237.</ref>


=Smoking assoc. disease=
=Smoking assoc. disease=
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*RBILD = respiratory bronchiolitis interstitial lung disease.
*RBILD = respiratory bronchiolitis interstitial lung disease.
*DIP = desquamative interstitial pneumonia.
*DIP = desquamative interstitial pneumonia.
*Eosinophilic granuloma (of lung) - AKA pulmonary langerhans cell histiocytosis.
*Eosinophilic granuloma (of lung) - [[AKA]] pulmonary langerhans cell histiocytosis.


All of the above are assoc. with smoking.  RBILD & DIP are considered by many to be on a continuum, i.e. RBILD is early DIP.
All of the above are assoc. with smoking.  RBILD & DIP are considered by many to be on a continuum, i.e. RBILD is early DIP.
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*Amiodarone toxicity, fibrotic NSIP - may appear similar.
*Amiodarone toxicity, fibrotic NSIP - may appear similar.


==Eosinophilic granuloma of lung==
==Pulmonary Langerhans cell histiocytosis==
*Assoc. with smoking.
===General===
*[[AKA]] eosinophilic granuloma of lung.
*Associated with smoking.<ref name=ppp234>PPP P.234.</ref>
*Not assoc. with systemic diseases of Langerhans cells (AKA Hand-Schueller-Christian disease).
 
Subtypes:<ref name=ppp234/>
*Cellular form.
*Fibrotic form.
 
One form usually predominates.


===Radiology===
===Radiology===
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===Histology===
===Histology===
Features:<ref>PPP P.237.</ref>
*Cellular peribronchiolar nodules with:
*Cellular peribronchiolar nodules with:
**Eosinophils - may be rare.
**Langerhans cells:
**Langerhans cells.
***Pale staining nucleus (H&E) with nuclear infolding - "crumpled tissue paper" appearance.
**Smoker's macrophages (brown pigmented airspace macrophages).
**+/-Smoker's macrophages (brown pigmented airspace macrophages).
**Chronic inflammatory cells (lymphocytes).
**+/-Eosinophilia (may be rare).
**Chronic inflammatory cells (lymphocytes). (???)
 
===IHC===
*Langerhans cells: S100+ and CD1a+.<ref>PPP P.237.</ref>


=Miscellaneous diseases=
=Miscellaneous diseases=
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