Arteries: Difference between revisions

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==Presentations==
<gallery>
File:Arterial aneurysm.jpg|link=Aneurysm|'''[[Aneurysm]]'''
</gallery>
*[[Thrombus]]
==Gross processing==
==Gross processing==
A minimal gross processing of arteries includes a longitudinal dissection and inspection of tunica intima.
A minimal gross processing of arteries includes a longitudinal dissection and inspection of tunica intima.
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==Microscopic examination==
==Microscopic examination==
*Look for atherosclerosis and thrombosis.
*Confirm that it is '''actually an artery''' (may be a vein, and a neuron may look grossly like a small artery).
*Estimate the maximum percentage of stenosis for each artery. Cross-sections collapse more or less after cutting, and estimations should be made as if the walls again took a circular shape.
*Look for '''atherosclerosis''' and '''[[thrombosis]]'''.
*Classify atherosclerosis as '''mild, moderate or severe'''.
*If cross-sections were made, estimate the '''maximum percentage of occlusion''' for each artery.  


<gallery mode=packed heights=220>
<gallery mode=packed heights=210>
File:Histopathology of pre-atherosclerotic intimal lesions.jpg|Histopathology of '''pre-atherosclerotic intimal lesions''': Intimal thickening (A) consists mainly of smooth muscle cells in a proteoglycan-rich matrix. Intimal xanthoma (B) displays intimal thickening with isolated foam cells (arrows).<ref name="YangFisher2017">{{cite journal|last1=Yang|first1=Wen Jie|last2=Fisher|first2=Mark|last3=Zheng|first3=Lu|last4=Niu|first4=Chun Bo|last5=Paganini-Hill|first5=Annlia|last6=Zhao|first6=Hai Lu|last7=Xu|first7=Yun|last8=Wong|first8=Ka Sing|last9=Ng|first9=Ho Keung|last10=Chen|first10=Xiang Yan|title=Histological Characteristics of Intracranial Atherosclerosis in a Chinese Population: A Postmortem Study|journal=Frontiers in Neurology|volume=8|year=2017|issn=1664-2295|doi=10.3389/fneur.2017.00488}}</ref>
File:Histopathology of pre-atherosclerotic intimal lesions.jpg|Histopathology of '''pre-atherosclerotic intimal lesions''': Intimal thickening (A) consists mainly of smooth muscle cells in a proteoglycan-rich matrix. Intimal xanthoma (B) displays intimal thickening with isolated foam cells (arrows).<ref name="YangFisher2017">{{cite journal|last1=Yang|first1=Wen Jie|last2=Fisher|first2=Mark|last3=Zheng|first3=Lu|last4=Niu|first4=Chun Bo|last5=Paganini-Hill|first5=Annlia|last6=Zhao|first6=Hai Lu|last7=Xu|first7=Yun|last8=Wong|first8=Ka Sing|last9=Ng|first9=Ho Keung|last10=Chen|first10=Xiang Yan|title=Histological Characteristics of Intracranial Atherosclerosis in a Chinese Population: A Postmortem Study|journal=Frontiers in Neurology|volume=8|year=2017|issn=1664-2295|doi=10.3389/fneur.2017.00488}}</ref>
File:Histopathology of progressive atherosclerotic lesions.jpg|Histopathology of '''progressive atherosclerotic lesions''': Pathological intima thickening (A) has some extracellular lipid (EL) present deep in the lesion without true necrosis. Fibrous cap atheroma (B) has a well-formed necrotic core (NC) containing lipids with an overlying thick fibrous cap (FC). Fibrocalcific plaques (C) are heavily calcified lesions with or without a necrotic core.<ref name="YangFisher2017"/>
File:Histopathology of progressive atherosclerotic lesion with extracellular lipid.jpg|A '''progressive atherosclerotic lesion''': Pathological intima thickening (A) has some extracellular lipid (EL) present deep in the lesion without true necrosis.<ref name="YangFisher2017"/>
File:Histopathology of plaque components in atherosclerosis.jpg|Histopathology of '''plaque components''' in atherosclerosis: (A) Intraplaque neovasculature (arrows); (B) intraplaque hemorrhage; (C) large areas of calcification seen as purple morula; (D) lumen thrombus (arrowhead); stained with hematoxylin and eosin (H&E); (E) macrophage infiltration; stained with CD68 antibodies.<ref name="YangFisher2017"/>
File:Histopathology of progressive atherosclerotic lesion with fibrous cap and necrotic core.jpg|'''Progressive lesion''': A fibrous cap atheroma has a well-formed necrotic core (NC) containing lipids with an overlying thick fibrous cap (FC).<ref name="YangFisher2017"/>
File:Histopathology of a fibrocalcific atheroma.jpg|'''Progressive lesion''': Fibrocalcific plaques are heavily calcified lesions with or without a necrotic core.<ref name="YangFisher2017"/>
File:Histopathology of plaque components in atherosclerosis.jpg|Histopathology of '''plaque components''' in atherosclerosis: (A) Intraplaque neovasculature (arrows); (B) intraplaque hemorrhage; (C) large areas of calcification seen as purple morula; (D) lumen [[thrombus]] (arrowhead); stained with hematoxylin and eosin (H&E); (E) macrophage infiltration; stained with CD68 antibodies.<ref name="YangFisher2017"/>
File:Histopathology of coronary artery atherosclerosis, annotated.jpg|Cross-sections collapse more or less after cutting, and estimations of the '''maximum percentage of stenosis''' should be made as imagined on an expanded blood vessel, as: 1-(lumen area)/(atherosclerosis area). In this case, there is 45-50% stenosis.
</gallery>
</gallery>
[[File:Histopathology of giant cell arteritis.png|thumb|400px|Evaluate for '''giant cell arteritis''' at least upon request. It is characterized by a granulomatous inflammation of arteries with discontinuous and fragmented internal elastic lamina.<ref>{{cite web|url=https://www.pathologyoutlines.com/topic/eyeorbittemporalarteritis.html|title=Eye - Orbit & optic nerve - Temporal arteritis|author=Nat Pernick, M.D.|website=PathologyOutlines}} Last author update: 1 February 2014. Last staff update: 29 December 2020</ref>]]


===Microscopy report===
===Microscopy report===
*Maximum percentage of stenosis for each artery.
*Classify any atherosclerosis as mild, moderate or severe.
*If cross-sections were made, state the maximum percentage of stenosis for each artery.
 
Example:
{|class=wikitable
| Sections of the three main coronary arteries reveal << mild / moderate / severe>> atherosclerosis, with approximately __%, __% and __% stenosis of the left anterior descending, left circumflex coronary artery and right coronary artery, respectively.
|}
{{Bottom}}
{{Bottom}}

Latest revision as of 14:59, 19 June 2022

Author: Mikael Häggström [note 1]

Presentations

Gross processing

A minimal gross processing of arteries includes a longitudinal dissection and inspection of tunica intima.

Consecutive cross-sections allows for a detection and estimation of atherosclerotic stenosis.

File:Plaque at different degrees of atherosclerotic stenosis.jpg
Plaque at different degrees of atherosclerotic stenosis.

Microscopic examination

  • Confirm that it is actually an artery (may be a vein, and a neuron may look grossly like a small artery).
  • Look for atherosclerosis and thrombosis.
  • Classify atherosclerosis as mild, moderate or severe.
  • If cross-sections were made, estimate the maximum percentage of occlusion for each artery.
File:Histopathology of giant cell arteritis.png
Evaluate for giant cell arteritis at least upon request. It is characterized by a granulomatous inflammation of arteries with discontinuous and fragmented internal elastic lamina.[2]

Microscopy report

  • Classify any atherosclerosis as mild, moderate or severe.
  • If cross-sections were made, state the maximum percentage of stenosis for each artery.

Example:

Sections of the three main coronary arteries reveal << mild / moderate / severe>> atherosclerosis, with approximately __%, __% and __% stenosis of the left anterior descending, left circumflex coronary artery and right coronary artery, respectively.

Notes

  1. For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.

Main page

References

  1. 1.0 1.1 1.2 1.3 1.4 Yang, Wen Jie; Fisher, Mark; Zheng, Lu; Niu, Chun Bo; Paganini-Hill, Annlia; Zhao, Hai Lu; Xu, Yun; Wong, Ka Sing; et al. (2017). "Histological Characteristics of Intracranial Atherosclerosis in a Chinese Population: A Postmortem Study ". Frontiers in Neurology 8. doi:10.3389/fneur.2017.00488. ISSN 1664-2295. 
  2. Nat Pernick, M.D.. Eye - Orbit & optic nerve - Temporal arteritis. PathologyOutlines. Last author update: 1 February 2014. Last staff update: 29 December 2020

Image sources