Hamman-Rich syndrome pathophysiology: Difference between revisions
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==Microscopic Pathology== | ==Microscopic Pathology== | ||
*On microscopic histopathological analysis | *On microscopic [[Histopathology|histopathological analysis]], [[Hamman-Rich syndrome|Acute interstitial pneumonitis]] will show following features: | ||
*Diffuse alveolar damage | **[[Diffuse alveolar damage]] | ||
*Hyaline membrane formation | **[[Hyaline]] membrane formation | ||
*Interstitial fibrosis: | **[[Interstitial lung disease|Interstitial fibrosis]]: | ||
**It is diffuse, uniform temporally with extensive fibroblastic and myofibroblastic proliferation and relatively less collagen deposition. | ***It is [[diffuse]], [[Uniform distribution|uniform]] temporally with extensive [[Fibroblast|fibroblastic]] and [[Myofibroblast|myofibroblastic]] proliferation and relatively less [[collagen]] deposition. | ||
**The uniformity of the fibroblastic/myofibroblastic proliferation and prominent activity distinguish AIP from the other types of idiopathic interstitial pneumonia. | ***The [[Uniform distribution|uniformity]] of the [[Fibroblast|fibroblastic]]/[[Myofibroblast|myofibroblastic]] proliferation and prominent activity distinguish AIP from the other types of idiopathic interstitial pneumonia. | ||
*Thickening and distortion of alveolar septa caused by spindle cell proliferation. | **Thickening and distortion of [[Alveolus|alveolar]] [[Septum (disambiguation)|septa]] caused by spindle cell [[Cell growth|proliferation]]. | ||
*Intraluminal polypoid plugs | **Intraluminal polypoid plugs | ||
*Organizing thrombi in small and medium-sized arteries | **Organizing [[Thrombus|thrombi]] in small and medium-sized [[Artery|arteries]] | ||
==References== | ==References== |
Revision as of 18:04, 20 March 2018
Overview
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
The exact pathogenesis of [disease name] is not fully understood.
OR
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to [disease name] usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype.
Pathophysiology
Pathogenesis
- The exact pathogenesis of [disease name] is not fully understood.
OR
- It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to [disease name] usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
Genetics
- [Disease name] is transmitted in [mode of genetic transmission] pattern.
- Genes involved in the pathogenesis of [disease name] include [gene1], [gene2], and [gene3].
- The development of [disease name] is the result of multiple genetic mutations.
Associated Conditions
Gross Pathology
- On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Microscopic Pathology
- On microscopic histopathological analysis, Acute interstitial pneumonitis will show following features:
- Diffuse alveolar damage
- Hyaline membrane formation
- Interstitial fibrosis:
- It is diffuse, uniform temporally with extensive fibroblastic and myofibroblastic proliferation and relatively less collagen deposition.
- The uniformity of the fibroblastic/myofibroblastic proliferation and prominent activity distinguish AIP from the other types of idiopathic interstitial pneumonia.
- Thickening and distortion of alveolar septa caused by spindle cell proliferation.
- Intraluminal polypoid plugs
- Organizing thrombi in small and medium-sized arteries