Difference between revisions of "Diffuse lung diseases"

Jump to navigation Jump to search
(→‎General: more)
Line 89: Line 89:
*Abbreviated ''UIP''.
*Abbreviated ''UIP''.
===General===
===General===
*It is sometimes used incorrectly as a synoym for ''idiopathic pulmonary fibrosis''.
*It is sometimes used incorrectly as a synonym for ''idiopathic pulmonary fibrosis''.  It is a histomorphologic pattern and has a DDx (see below).
*Cannot be diagnosed via bronchoscopic or transbronchial biopsy.<ref name=Ref_PPP186>{{Ref PPP|186}}</ref>
*UIP cannot be diagnosed via bronchoscopic or transbronchial biopsy,<ref name=Ref_PPP186>{{Ref PPP|186}}</ref> as it is peripheral.


====Epidemiology====
====Epidemiology====
Line 108: Line 108:
**Usually subplural, i.e. peripheral lung.
**Usually subplural, i.e. peripheral lung.
**Classically lower lobe predominant.
**Classically lower lobe predominant.
**Associated with interstitial thickening. (???)
*Traction bronchiectasis.


Note:
Note:
*Cysts - have thin walls (think of emphysema, lymphangioleiomyomatosis et cetera).
*Cysts - have thin walls (think of emphysema, [[lymphangioleiomyomatosis]] et cetera).
**Cysts may be isolated/not close to a neighbour.
**Cysts may be isolated/not close to a neighbour.
**Medcyclopaedia defines it as: thin-walled, well-demarcated and >1 cm.<ref>[http://www.medcyclopaedia.com/library/topics/volume_v_1/l/lung_cyst.aspx http://www.medcyclopaedia.com/library/topics/volume_v_1/l/lung_cyst.aspx]</ref>
**Medcyclopaedia defines it as: thin-walled, well-demarcated and >1 cm.<ref>[http://www.medcyclopaedia.com/library/topics/volume_v_1/l/lung_cyst.aspx http://www.medcyclopaedia.com/library/topics/volume_v_1/l/lung_cyst.aspx]</ref>
Line 121: Line 121:
**Location: in the areas of transisition between active inflammation and old inflammation.<ref>[http://www.epler.com/IPFWhat%27sIPFDiseaseInformation2.htm http://www.epler.com/IPFWhat%27sIPFDiseaseInformation2.htm]</ref>
**Location: in the areas of transisition between active inflammation and old inflammation.<ref>[http://www.epler.com/IPFWhat%27sIPFDiseaseInformation2.htm http://www.epler.com/IPFWhat%27sIPFDiseaseInformation2.htm]</ref>
**Note: Technically, ''fibroblast foci'' are composed of myofibroblasts.<ref name=Ref_PPP189>{{Ref PPP|189}}</ref>
**Note: Technically, ''fibroblast foci'' are composed of myofibroblasts.<ref name=Ref_PPP189>{{Ref PPP|189}}</ref>
*Interstitial inflammation,
*Interstitial inflammation.
*Microscopic honeycombing,
*Microscopic honeycombing.
**Typically peripheral - cysts lined by ciliated epithelium.
**Typically peripheral - cysts lined by ciliated epithelium.
*Spatial heterogeneity - patchy lesional distribution (areas of abnormal and normal lung may appear beside one another).
*Spatial heterogeneity - patchy lesional distribution (areas of abnormal and normal lung may appear beside one another).
*Temporal heterogeneity - lesions of differing age side-by-side.<ref>H. 8 July, 2009.</ref>
*Temporal heterogeneity - lesions of differing age side-by-side.<ref name=Ref_WMSP92>{{Ref WMSP|92}}</ref>


Notes:
Notes:
48,460

edits

Navigation menu