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Arteriolosclerosis

From Wikipedia, the free encyclopedia
Hardening of small arteries (arterioles)
Medical condition
Arteriolosclerosis
Right breast mammograms showing several calcified arterioles. Patient 94 years old.
SpecialtyCardiology Edit this on Wikidata

Arteriolosclerosis is a form ofcardiovascular disease involving hardening and loss of elasticity ofarterioles orsmallarteries and is most often associated withhypertension anddiabetes mellitus.[1]Types includehyaline arteriolosclerosis andhyperplastic arteriolosclerosis,[2] both involved withvessel wall thickening andluminal narrowing that may cause downstreamischemic injury.The following two terms whilst similar, are distinct in both spelling and meaning and may easily be confused with arteriolosclerosis.

Micrograph showing hyaline arteriolosclerosis in thekidney.PAS stain.

Hyaline arteriolosclerosis

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Alsoarterial hyalinosis andarteriolar hyalinosis refers to thickening of the walls of arterioles by the deposits that appear as homogeneous pinkhyaline material in routine staining.[3] It is a type of arteriolosclerosis, which refers to thickening of thearteriolar wall and is part of the aging process.[4]

Associations

It is associated withaging,hypertension,diabetes mellitus,[5]dementia,[6] and may be seen in response to certain drugs (calcineurin inhibitors).[7]

It is often seen in the context of kidney pathology.[4][8][9] In hypertension only the afferent arteriole is affected, while in diabetes mellitus, both theafferent andefferent arteriole are affected.[8][9] It is also seen in retina and brain,[10] whereretinal infarcts andsmall brain infarcts, or lacunes can occur.

Cause

Lesions reflect leakage ofplasma components acrossvascularendothelium and excessiveextracellular matrix production bysmooth muscle cells, usually secondary to hypertension.[11]

Hyaline arteriolosclerosis is a major morphologic characteristic ofbenign nephrosclerosis, in which the arteriolar narrowing causes diffuse impairment ofrenalblood supply, with loss ofnephrons.[5] The narrowing of the lumen can decrease renal blood flow and henceglomerular filtration rate leading to increasedrenin secretion and a perpetuating cycle with increasing blood pressure and decreasing kidney function.[12]

The brain is another organ where hyaline arteriolosclerosis occurs prematurely in patients with high blood pressure. This can cause either kind ofstroke: anischemic infarct or abrain hemorrhage, as the vessels can be blocked or broken.[13]

Hyperplastic arteriolosclerosis

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"Onion-skin" renal arteriole

This is a type of arteriolosclerosis involving a narrowedlumen.[4]The term "onion-skin" is sometimes used to describe this form of blood vessel[14] with thickened concentric smooth muscle cell layer and thickened, duplicated basement membrane. Inmalignant hypertension these hyperplastic changes are often accompanied by fibrinoid necrosis of the arterial intima and media. These changes are most prominent in thekidney and can lead to ischemia and acutekidney failure. In the brain, a small cavity called a lacune is an ischemic cavity that can arise due to brain necrosis, due to arteriolosclerosis.[15][16]

Cause

It can be caused by malignant hypertension.[4][17]

References

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  1. ^Robbins, Stanley L.; Kumar, Vinay (2007).Robbins basic pathology. Saunders/Elsevier. p. 343.ISBN 978-0-8089-2366-4.
  2. ^"Arteriolosclerosis" atDorland's Medical Dictionary
  3. ^Gamble CN (March 1986)."The pathogenesis of hyaline arteriolosclerosis".Am. J. Pathol.122 (3):410–20.PMC 1888226.PMID 2420184.
  4. ^abcdThomas H. McConnell (2007).The Nature of Disease: Pathology for the Health Professions. Lippincott Williams & Wilkins. pp. 277–.ISBN 978-0-7817-5317-3.
  5. ^abRobbins, Stanley L.; Kumar, Vinay (2007).Robbins basic pathology. Saunders/Elsevier. p. 356.ISBN 978-0-8089-2366-4.
  6. ^Hainsworth AH, Markus HS, Schneider JA (2024)."Cerebral Small Vessel Disease, Hypertension, and Vascular Contributions to Cognitive Impairment and Dementia".Hypertension.81 (1):75–86.doi:10.1161/HYPERTENSIONAHA.123.19943.PMC 10734789.PMID 38044814.
  7. ^Yagisawa T, Omoto K, Shimizu T, Ishida H, Tanabe K (2015)."Arteriosclerosis in zero-time biopsy is a risk factor for tacrolimus-induced chronic nephrotoxicity".Nephrology (Carlton). 20 Suppl 2:51–7.doi:10.1111/nep.12461.PMID 26031587.
  8. ^abStout LC, Kumar S, Whorton EB (1994). "Insudative lesions--their pathogenesis and association with glomerular obsolescence in diabetes: a dynamic hypothesis based on single views of advancing human diabetic nephropathy".Human Pathology.25 (11):1213–1227.doi:10.1016/0046-8177(94)90039-6.PMID 7959667.
  9. ^abNajafian B, Alpers CE, Fogo AB (2011). "Pathology of human diabetic nephropathy".Contributions to Nephrology.170:36–47.doi:10.1159/000324942.ISBN 978-3-8055-9742-5.PMID 21659756.
  10. ^Lindley RI, Wang JJ, Wong MC, Mitchell P, Liew G, Hand P, Wardlaw J, De Silva DA, Baker M, Rochtchina E, Chen C, Hankey GJ, Chang HM, Fung VS, Gomes L, Wong TY (2009)."Retinal microvasculature in acute lacunar stroke: a cross-sectional study".Lancet Neurology.8 (7):628–634.doi:10.1016/S1474-4422(09)70131-0.PMID 19481977.
  11. ^Eva Brehmer-Andersson (2006-08-02).Dermatopathology. Springer Science & Business Media. pp. 75–.ISBN 978-3-540-30244-5.
  12. ^Sealey JE, von Lutterotti N, Rubattu S, Campbell WG Jr, Gahnem F, Halimi JM, Laragh JH (1991). "The greater renin system. Its prorenin-directed vasodilator limb. Relevance to diabetes mellitus, pregnancy, and hypertension".American Journal of Hypertension.4 (12 Part 1):972–977.doi:10.1093/ajh/4.12.972.PMID 1815656.
  13. ^Sutherland GR, Auer RN (2006). "Primary intracerebral hemorrhage".Journal of Clinical Neuroscience.13 (5):511–517.doi:10.1016/j.jocn.2004.12.012.PMID 16769513.
  14. ^"Pathology Education". Archived fromthe original on 2006-09-01. Retrieved2009-01-12.
  15. ^Fisher CM (December 1968). "The arterial lesions underlying lacunes".Acta Neuropathologica.12 (1):1–15.doi:10.1007/BF00685305.PMID 5708546.
  16. ^Fisher CM (1971). "Pathological observations in hypertensive cerebral hemorrhage".Journal of Neuropathology and Experimental Neurology.30 (3):536–550.doi:10.1097/00005072-197107000-00015.PMID 4105427.
  17. ^"Atherosclerosis". Retrieved2009-01-12.

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Classification
Arteries,arterioles
andcapillaries
Inflammation
Arteriosclerosis
Peripheral artery disease
Aneurysm /dissection /
pseudoaneurysm
Vascular malformation
Vascular nevus
Veins
Inflammation
Venous thrombosis /
Thrombophlebitis
Varicose veins
Other
Arteries or veins
Blood pressure
Hypertension
Hypotension
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