Gallstone disease pathophysiology: Difference between revisions

Jump to navigation Jump to search
No edit summary
 
(50 intermediate revisions by 5 users not shown)
Line 1: Line 1:
<div style="-webkit-user-select: none;">
{| class="infobox" style="position: fixed; top: 65%; right: 10px; margin: 0 0 0 0; border: 0; float: right;"
{| class="infobox" style="position: fixed; top: 65%; right: 10px; margin: 0 0 0 0; border: 0; float: right;"
|-
|-
| {{#ev:youtube|https://https://www.youtube.com/watch?v=UPw3ot1M_o0|350}}
|{{#ev:youtube|https://https://www.youtube.com/watch?v=UPw3ot1M_o0|350}}
|-
|-
|}
|}
Line 10: Line 9:


==Overview==
==Overview==
It has long been noted that gallbladder stone formation is associated with bile supersaturation, and this still remains the most common cause for gallstone formation.<ref name="pmid17981556">{{cite journal |vauthors=Wang HH, Portincasa P, Wang DQ |title=Molecular pathophysiology and physical chemistry of cholesterol gallstones |journal=Front. Biosci. |volume=13 |issue= |pages=401–23 |year=2008 |pmid=17981556 |doi= |url=}}</ref>


== Pathophysiology ==
Studies have shown that [[Gallstone disease|gallstone]] formation is mostly due to [[bile]] [[supersaturation]]. In the [[United States]], patients that present with [[gallbladder]] stones mostly have [[cholesterol]] stones. [[Cholesterol]] stones form when the [[concentration]] of [[cholesterol]] in the [[bile]] is much higher than the [[concentration]] of [[cholesterol]] that can be dissolved in the [[bile]]. Normally [[cholesterol]] is [[Metabolism|metabolized]] in the body and excess [[cholesterol]] is disposed of in the bile. There is a balance between pronucleating (crystallization-promoting) and antinucleating (crystallization-inhibiting) forces, so that gallstones don't form. When pronucleating forces take the upper hand, gallstones will form. On the other hand, moderate intake of wine and the consumption of whole grain bread may decrease the risk of developing gallstones.
==Pathophysiology==


[[Image:Gallstones.jpg|thumb|200px|left|[[Gall bladder]] opened to show numerous '''gallstones'''. Their brownish to greenish color suggest they are cholesterol [[Calculus (medicine)|calculi]]. Source: Wikimedia Commons<ref>name="urlFile:Gallensteine 2006 03 28.JPG - Wikimedia Commons">{{cite web |url=https://commons.wikimedia.org/wiki/File:Gallensteine_2006_03_28.JPG |title=File:Gallensteine 2006 03 28.JPG - Wikimedia Commons |format= |work= |accessdate=}}</ref>]]
*The most common type of gallstone is a [[cholesterol]] stone.<ref name="pmid22570746">{{cite journal |vauthors=Stinton LM, Shaffer EA |title=Epidemiology of gallbladder disease: cholelithiasis and cancer |journal=Gut Liver |volume=6 |issue=2 |pages=172–87 |year=2012 |pmid=22570746 |pmc=3343155 |doi=10.5009/gnl.2012.6.2.172 |url=}}</ref><ref name="pmid12242178">{{cite journal |vauthors=Indar AA, Beckingham IJ |title=Acute cholecystitis |journal=BMJ |volume=325 |issue=7365 |pages=639–43 |year=2002 |pmid=12242178 |pmc=1124163 |doi= |url=}}</ref><ref>{{cite book | last = McPhee | first = Stephen | title = Pathophysiology of disease : an introduction to clinical medicine | publisher = McGraw-Hill Education Medical | location = New York | year = 2014 | isbn = 0071806008 }}</ref><ref name="pmid17981556">{{cite journal |vauthors=Wang HH, Portincasa P, Wang DQ |title=Molecular pathophysiology and physical chemistry of cholesterol gallstones |journal=Front. Biosci. |volume=13 |issue= |pages=401–23 |year=2008 |pmid=17981556 |doi= |url=}}</ref><ref>{{cite journal |year=1995  |title=. |journal=European Journal Gastroenterology & Hepatology |volume=6 |pages=585-593 |accessdate= 2007-08-25}}</ref>
*When pronucleating proteins are present, such as [[mucin]], the [[bile]] becomes [[Supersaturation|hypersaturated]] with [[cholesterol]] and [[cholesterol]] stones form.
*Gallstone disease can also be caused by a lack of [[motility]] in the [[muscular]] wall of the [[gallbladder]] or excessive [[Sphincter of Oddi|sphincter]] contraction, that prevents [[bile]] secretion.
*In this way the [[bile]] stagnates within the gallbladder and promotes the formation of stones.


It is thought that Gallstone disease is caused by bile hypersaturation, meaning that the bile becomes over saturated with a particular substance more than can be dissolved in the bile.
===Pathogenesis of Specific Stones===


One of the most important substances that can lead to stone formation is Cholesterol.  
*[[Cholesterol]] stones are the most common type of gallstone.
*The quantity of [[cholesterol]] is balanced within the body.
*[[Cholesterol]] is an important [[Organic Chemistry|organic]] molecule that is needed for incorporation within [[Cell membrane|cell membranes]] and to produce [[Steroid hormone|steroid hormones]] in the body.


Cholesterol is an important substance that is needed to form cell membranes and to produce steroid hormones in the body.
<br>
 
<div style="text-align: center;">'''Cholesterol Stones Formation'''<ref name="pmid22570746">{{cite journal |vauthors=Stinton LM, Shaffer EA |title=Epidemiology of gallbladder disease: cholelithiasis and cancer |journal=Gut Liver |volume=6 |issue=2 |pages=172–87 |year=2012 |pmid=22570746 |pmc=3343155 |doi=10.5009/gnl.2012.6.2.172 |url=}}</ref><ref name="pmid17547709">{{cite journal |vauthors=Marschall HU, Einarsson C |title=Gallstone disease |journal=J. Intern. Med. |volume=261 |issue=6 |pages=529–42 |year=2007 |pmid=17547709 |doi=10.1111/j.1365-2796.2007.01783.x |url=}}</ref><ref name="pmid18579815">{{cite journal |vauthors=Strasberg SM |title=Clinical practice. Acute calculous cholecystitis |journal=N. Engl. J. Med. |volume=358 |issue=26 |pages=2804–11 |year=2008 |pmid=18579815 |doi=10.1056/NEJMcp0800929 |url=}}</ref></div>
Its quantity must be balanced internally and the only way in which the body can rid itself of it is through the bile.
<br>
 
{| align="center"
The process of stone formation begins with the presence of biliary sludge.
|
 
{{Family tree/start}}
This thick compound consists of glycoproteins, calcium deposits, and cholesterol crystals in the gallbladder.
{{Family tree | | | | A01 | | | |A01=Excess [[cholesterol]] in body}}
 
{{Family tree | | | | |!| | | | | }}
This precipitation is also called "crystallization".   
{{Family tree | | | | B01 | | | |B01=The body will dispose of it by secreting it into the [[bile]]}}
 
{{Family tree | | | | |!| | | | | }}
Usually there are antagonistic mechanisms in place that work to prevent cholesterol from precipitating or crystallizing in the bile.
{{Family tree | | | | C01 | | | |C01=[[Cholesterol]] [[concentration]] reaches a certain level beyond that that can be secreted into the bile}}
{{Family tree | | | | |!| | | | | }}
{{Family tree | | | | D01 | | | |D01=[[Biliary]] sludge starts to form}}
{{Family tree | | | | |!| | | | | }}
{{Family tree | | | | E01 | | | |E01=[[Biliary]] sludge is a [[Viscosity|viscous]] mixture that consists of [[mucin]] [[Glycoprotein|glycoproteins]], [[Calcium|calcium deposits]] and [[cholesterol]] crystals in the gallbladder}}
{{Family tree | | | | |!| | | | | }}
{{Family tree | | | | F01 | | | |F01=Over time, the sludge becomes more and more concentrated with [[cholesterol]]}}
{{Family tree | | | | |!| | | | | }}
{{Family tree | | | | G01 | | | |G01= Eventually forming gallstones}}
{{Family tree/end}}
|}
====Pigment Stones====


These include: pronucleating (crystallization-promoting) and antinucleating (crystallization-inhibiting) factors.  
*Less commonly, gallstones can be composed of [[bilirubin]] and are sometimes referred to as "pigment stones".<ref name="pmid2022417">{{cite journal |vauthors=Trotman BW |title=Pigment gallstone disease |journal=Gastroenterol. Clin. North Am. |volume=20 |issue=1 |pages=111–26 |year=1991 |pmid=2022417 |doi= |url=}}</ref>
*[[Bilirubin]] is a byproduct of [[red blood cell]] [[Hemolysis|breakdown]] and so are usually found in patients with [[Hemoglobinopathy|hemoglobin disorders]].
*Pigment stones are formed via two main pathways:
**[[Infection]] of the [[biliary tree]] with [[bacteria]] that can release [[Hydrolysis|hydrolytic]] enzymes and form insoluble [[calcium]] salts.
**Non-bacterial, non-enzymatic hydrolysis of [[bilirubin]] conjugates such as what may happen in patients with [[Gilbert's syndrome]] and [[Hemolysis|chronic hemolysis]].


Furthermore, the lack of motility in the muscular wall of the gallbladder or the excessive sphincter contraction, that prevents bile secretion may also contribute to stone formation.
====Mixed Stones====


This causes bile to stagnate within the gallbladder.  
*There is a lack of evidence that supports a true pathology to explain how mixed stones are formed.<ref name="pmid12242178">{{cite journal |vauthors=Indar AA, Beckingham IJ |title=Acute cholecystitis |journal=BMJ |volume=325 |issue=7365 |pages=639–43 |year=2002 |pmid=12242178 |pmc=1124163 |doi= |url=}}</ref>
*However, there have been theories that include a combination of several mechanisms including supersaturation, [[infection]] and hypomotility of the [[gall bladder]].


Rarely, the gallbladder may not properly fill with bile and so the bile is instead diverted from the gallbladder to the small bile duct.
==Associated Conditions==
 
The conditions associated with gallstone disease include:<ref name="pmid29158491">{{cite journal |vauthors=Lv J, Yu C, Guo Y, Bian Z, Yang L, Chen Y, Li S, Huang Y, Fu Y, He P, Tang A, Chen J, Chen Z, Qi L, Li L |title=Gallstone Disease and the Risk of Type 2 Diabetes |journal=Sci Rep |volume=7 |issue=1 |pages=15853 |year=2017 |pmid=29158491 |doi=10.1038/s41598-017-14801-2 |url=}}</ref><ref>{{cite journal |vauthors=Ortega RM, et al. |year=1997 |title=Differences in diet and food habits between patients with gallstones and controls |journal=Journal of the American College of Nutrition |volume= 16 |pages=88-95 |accessdate= 2007-08-25}}</ref>
This exacerbates the hypomotility and accelerates stone formation.
 
Occasionally, gallstones are composed of bilirubin and can be referred to as "pigment stones".
 
Bilirubin is a byproduct of red blood cell breakdown.
 
These stones are formed via two main pathways:
 
1. An infection of the biliary tract can predispose to stone formation.
2.Bile is normally recycled after its secretion back from the small bowel and to the liver. If there is increased enterohepatic cycling this may also cause the formation of a bilirubin stone. Pigment stones are seen more often in the Asian and African continents.
 
 
 
 
 
===Associated Conditions===  


*[[Diabetes mellitus type 2|Diabetes mellitus type 2]]
*[[Diabetes mellitus type 2|Diabetes mellitus type 2]]
*[[Obesity]]
*[[Obesity]]
*[[Pregnancy]]
*[[Pregnancy]]
*[[Cholangiocarcinoma|Gallbladder cancer]]
*[[Gallbladder cancer]]
*Gallbladder [[Polyp|polyps]]
*[[Gallbladder]] [[Polyp|polyps]]
*[[Primary sclerosing cholangitis|Primary sclerosing cholangitis]]
*[[Primary sclerosing cholangitis|Primary sclerosing cholangitis]]
*[[Porcelain gallbladder|Porcelain gallbladder]]
*[[Porcelain gallbladder|Porcelain gallbladder]]
Line 73: Line 77:
**Whole grain bread
**Whole grain bread
**Fiber
**Fiber
**[[Vitamin C]]<ref name="pmid29158491">{{cite journal |vauthors=Lv J, Yu C, Guo Y, Bian Z, Yang L, Chen Y, Li S, Huang Y, Fu Y, He P, Tang A, Chen J, Chen Z, Qi L, Li L |title=Gallstone Disease and the Risk of Type 2 Diabetes |journal=Sci Rep |volume=7 |issue=1 |pages=15853 |year=2017 |pmid=29158491 |doi=10.1038/s41598-017-14801-2 |url=}}</ref><ref>{{cite journal |author=R.M. Ortega |coauthors=M. Fernandez-Azuela, A. Encinas-Sotillos, P. Andres, and A. M. Lopez-Sobaler |year=1997 |month=February |title=Differences in diet and food habits between patients with gallstones and controls |journal=Journal of the American College of Nutrition |volume= 16 |pages=88-95 |accessdate= 2007-08-25}}</ref>
**[[Vitamin C]]
 
On the other hand, wine and whole grain bread may decrease the risk of gallstones.<ref>{{cite journal |year=1995 |month=June |title=. |journal=European Journal Gastroenterology & Hepatology |volume=6 |pages=585-593 |accessdate= 2007-08-25}}</ref>


==Gross Pathology==
==Gross Pathology==
[[Image:642x361_Gallstones_SLIDE_1.jpg|thumb|200px|left|[[Gall bladder]] opened to show numerous gallstones. Source: Wikimedia Commons<ref name="urlFile:Gallensteine 2006 03 28.JPG - Wikimedia Commons">{{cite web |url=https://commons.wikimedia.org/wiki/File:Gallensteine_2006_03_28.JPG |title=File:Gallensteine 2006 03 28.JPG - Wikimedia Commons |format= |work= |accessdate=}}</ref>]]


*On gross pathology, commonly multiple small stones are found and less commonly a solitary stone is seen.<ref>{{cite book | last = Ansert | first = Sandra | title = Textbook of diagnostic sonography | publisher = Elsevier | location = St. Louis, MO | year = 2018 | isbn = 978-0323353755}}</ref>


On gross pathology, multiple small stones are commonly found or less commonly a solitary stone is seen. The smaller stones represent a higher morbidity since they can easily occlude the [[Bile duct|biliary tracts]].<ref>{{cite book | last = Ansert | first = Sandra | title = Textbook of diagnostic sonography | publisher = Elsevier | location = St. Louis, MO | year = 2018 | isbn = 978-0323353755}}</ref>
[[Image:Gallstone.jpg|thumb|center|500px|Cholesterol gallstones are seen. Source: commons.wikimedia.org by Noortje123 from nl, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=1805918]]


==Microscopic Pathology==
==Microscopic Pathology==


On microscopic histopathological analysis, variable evidences of inflammation can be noted transmurally including [[Neutrophil|neutrophils]], which are characteristic in gallstone disease.<ref>{{cite book | last = Fisher | first = M. M. | title = Gallstones | publisher = Springer US | location = Boston, MA | year = 1979 | isbn = 1461570662 }}</ref>
*On microscopic analysis, characteristic findings include:<ref>{{cite book | last = Fisher | first = M. M. | title = Gallstones | publisher = Springer US | location = Boston, MA | year = 1979 | isbn = 1461570662 }}</ref>
**Transmural thickening of the gall bladder wall
**[[Neutrophilia]]


==References==
==References==
Line 94: Line 96:
{{WH}}
{{WH}}
{{WS}}
{{WS}}
[[Category: (name of the system)]]
 
[[Category:Gastroenterology]]
[[Category:Hepatology]]
[[Category:Surgery]]
[[Category:Disease]]

Latest revision as of 22:06, 22 December 2020

https://https://www.youtube.com/watch?v=UPw3ot1M_o0%7C350}}

Gallstone disease Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Gallstone disease from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

CT

MRI

Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Lithotripsy
Surgical management

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Gallstone disease pathophysiology On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Gallstone disease pathophysiology

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Gallstone disease pathophysiology

CDC on Gallstone disease pathophysiology

Gallstone disease pathophysiology in the news

Blogs on Gallstone disease pathophysiology

Directions to Hospitals Treating Gallstone disease

Risk calculators and risk factors for Gallstone disease pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hadeel Maksoud M.D.[2]

Overview

Studies have shown that gallstone formation is mostly due to bile supersaturation. In the United States, patients that present with gallbladder stones mostly have cholesterol stones. Cholesterol stones form when the concentration of cholesterol in the bile is much higher than the concentration of cholesterol that can be dissolved in the bile. Normally cholesterol is metabolized in the body and excess cholesterol is disposed of in the bile. There is a balance between pronucleating (crystallization-promoting) and antinucleating (crystallization-inhibiting) forces, so that gallstones don't form. When pronucleating forces take the upper hand, gallstones will form. On the other hand, moderate intake of wine and the consumption of whole grain bread may decrease the risk of developing gallstones.

Pathophysiology

Pathogenesis of Specific Stones


Cholesterol Stones Formation[1][6][7]


 
 
 
Excess cholesterol in body
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
The body will dispose of it by secreting it into the bile
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Cholesterol concentration reaches a certain level beyond that that can be secreted into the bile
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Biliary sludge starts to form
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Biliary sludge is a viscous mixture that consists of mucin glycoproteins, calcium deposits and cholesterol crystals in the gallbladder
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Over time, the sludge becomes more and more concentrated with cholesterol
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Eventually forming gallstones
 
 
 

Pigment Stones

Mixed Stones

  • There is a lack of evidence that supports a true pathology to explain how mixed stones are formed.[2]
  • However, there have been theories that include a combination of several mechanisms including supersaturation, infection and hypomotility of the gall bladder.

Associated Conditions

The conditions associated with gallstone disease include:[9][10]

Gross Pathology

  • On gross pathology, commonly multiple small stones are found and less commonly a solitary stone is seen.[11]
Cholesterol gallstones are seen. Source: commons.wikimedia.org by Noortje123 from nl, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=1805918

Microscopic Pathology

  • On microscopic analysis, characteristic findings include:[12]

References

  1. 1.0 1.1 Stinton LM, Shaffer EA (2012). "Epidemiology of gallbladder disease: cholelithiasis and cancer". Gut Liver. 6 (2): 172–87. doi:10.5009/gnl.2012.6.2.172. PMC 3343155. PMID 22570746.
  2. 2.0 2.1 Indar AA, Beckingham IJ (2002). "Acute cholecystitis". BMJ. 325 (7365): 639–43. PMC 1124163. PMID 12242178.
  3. McPhee, Stephen (2014). Pathophysiology of disease : an introduction to clinical medicine. New York: McGraw-Hill Education Medical. ISBN 0071806008.
  4. Wang HH, Portincasa P, Wang DQ (2008). "Molecular pathophysiology and physical chemistry of cholesterol gallstones". Front. Biosci. 13: 401–23. PMID 17981556.
  5. European Journal Gastroenterology & Hepatology. 6: 585–593. 1995. |access-date= requires |url= (help)
  6. Marschall HU, Einarsson C (2007). "Gallstone disease". J. Intern. Med. 261 (6): 529–42. doi:10.1111/j.1365-2796.2007.01783.x. PMID 17547709.
  7. Strasberg SM (2008). "Clinical practice. Acute calculous cholecystitis". N. Engl. J. Med. 358 (26): 2804–11. doi:10.1056/NEJMcp0800929. PMID 18579815.
  8. Trotman BW (1991). "Pigment gallstone disease". Gastroenterol. Clin. North Am. 20 (1): 111–26. PMID 2022417.
  9. Lv J, Yu C, Guo Y, Bian Z, Yang L, Chen Y, Li S, Huang Y, Fu Y, He P, Tang A, Chen J, Chen Z, Qi L, Li L (2017). "Gallstone Disease and the Risk of Type 2 Diabetes". Sci Rep. 7 (1): 15853. doi:10.1038/s41598-017-14801-2. PMID 29158491.
  10. Ortega RM, et al. (1997). "Differences in diet and food habits between patients with gallstones and controls". Journal of the American College of Nutrition. 16: 88–95. |access-date= requires |url= (help)
  11. Ansert, Sandra (2018). Textbook of diagnostic sonography. St. Louis, MO: Elsevier. ISBN 978-0323353755.
  12. Fisher, M. M. (1979). Gallstones. Boston, MA: Springer US. ISBN 1461570662.

Template:WH Template:WS