Non-alcoholic fatty liver disease other diagnostic studies: Difference between revisions

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{{Non alcoholic fatty liver disease}}
{{Non alcoholic fatty liver disease}}
'''Editor in Chief''': Elliot Tapper, M.D., Beth Israel Deaconess Medical Center, [[User:C Michael Gibson |C. Michael Gibson, M.S., M.D.]] [mailto:charlesmichaelgibson@gmail.com]
{{CMG}} ; {{AE}} {{ADG}}
 
==Overview==
==Overview==
A biopsy of the liver is still considered the gold standard in diagnosis. This is especially true for those patients with elevated liver enzymes for whom a non-invasive workup is inconclusive; 34% of these patients, in one series, were found to have NASH.<ref>Skelly et al. Findings on liver biopsy to investigate abnormal liver function tests in the absence of diagnostic serology. J Hepatol 2001;35:195-9
Liver biopsy may be helpful in the diagnosis of non-alcoholic fatty liver disease. Findings on biopsy include [[Steatosis|macrovesicular steatosis]], [[inflammation]], ballooning degeneration, zone 3 perivenular/periportal/perisinusoidal fibrosis and, finally, [[mallory bodies]].
</ref> Classically, biopsy reveals macrovesicular steatosis, inflammation, ballooning degeneration, zone 3 perivenular/periportal/perisinusoidal fibrosis and, finally, mallory bodies.<ref>Angula P. Nonalcoholic Fatty Liver Disease. NEJM. 2002 346(16):1221-31</ref><ref>Brunt EM, Janney CG, Di Bisceglie AM et al. Nonalcoholic steatohepatitis: A proposal for grading and staging the histological lesions. Am. J. Gastroenterol. 1999; 94(9):2467-2474</ref> Unfortunately, however, a standard biopsy is only able to sample a volume that is 1/50,000th of the liver, underscoring substantial room for sampling error.
==Other Diagnostic Studies==
*Liver biopsy is considered as a gold-standard for diagnosing, grading, and staging NAFLD.
*Invasive test
*Associated with significant bleeding risk in patients with [[Clotting|clotting abnormalities]] due to hepatic disease.
 
===Complications===
Complications of liver biopsy are rare but include
*[[Pain]]
*[[Hypotension]]
*[[Peritonitis]]
*[[Internal bleeding|Intraperitoneal hemorrhage]]
*Biliary injury
===Findings===
Classically, biopsy reveals:<ref>Angula P. Nonalcoholic Fatty Liver Disease. NEJM. 2002 346(16):1221-31</ref><ref>Brunt EM, Janney CG, Di Bisceglie AM et al. Nonalcoholic steatohepatitis: A proposal for grading and staging the histological lesions. Am. J. Gastroenterol. 1999; 94(9):2467-2474</ref>
*[[Steatosis|Macrovesicular steatosis]]
*[[Inflammatory cells]]
*Ballooning degeneration
*Zone 3 perivenular/periportal/perisinusoidal [[fibrosis]]
*[[Mallory bodies]]
===Interpretation===
*Histologic changes in NAFLD are very similar to those in [[alcoholic hepatitis]] and may also mimic those seen in chronic [[HCV infection]].
*The spectrum of abnormalities varies from simple bland [[steatosis]] to [[NASH]], in which [[steatosis]] is associated with mixed [[Inflammatory cells|inflammatory cell infiltration]], mostly lobular, and liver injury.
*Cell injury is manifested by hepatocyte ballooning as well as by Mallory hyaline and [[Acidophilic|acidophilic bodies]].
*[[Fibrosis]] is classically perisinusoidal/perivenular and may lead to bridging [[fibrosis]] and [[cirrhosis]].
*Although [[Portal system|portal tracts]] are relatively spared in adult NAFLD, children with this condition may have a predominance of portal [[inflammation]] and [[fibrosis]] as opposed to lobular involvement.
*Compared with [[alcoholic hepatitis]], NASH is associated with a higher prevalence of nuclear vacuoles and [[steatosis]], while [[alcoholic hepatitis]] tends to produce periportal and pericellular [[fibrosis]].
*[[Alcoholic hepatitis]] presents with identical [[histology]] but patient history and/or biochemistry will indicate prolonged, excessive [[alcohol]] intake.<ref>Skelly et al. Findings on liver biopsy to investigate abnormal liver function tests in the absence of diagnostic serology. J Hepatol 2001;35:195-9
</ref>
===Histo-pathological classification===
Depending on degree of steatosis, necroinflammatory activity, and degree of fibrosis non-alcoholic liver disease can be classified as follows:
 
===Grading===
NAFLD activity score is employed for grading steatohepatitis of NASH. NAS represents the sum of scores for [[steatosis]], lobular [[inflammation]], and ballooning.<ref name="pmid28507929">{{cite journal |vauthors=Vizuete J, Camero A, Malakouti M, Garapati K, Gutierrez J |title=Perspectives on Nonalcoholic Fatty Liver Disease: An Overview of Present and Future Therapies |journal=J Clin Transl Hepatol |volume=5 |issue=1 |pages=67–75 |year=2017 |pmid=28507929 |pmc=5411359 |doi=10.14218/JCTH.2016.00061 |url=}}</ref>
{| border="1" cellpadding="5" cellspacing="0" align="center" |class="wikitable"
! style="background:#efefef;" |Component
! style="background:#efefef;" |Range
! style="background:#efefef;" |Score
|-
| rowspan="4" |Steatosis
|<5%
|0
|-
|5-33%
|1
|-
|34-66%
|2
|-
|>66%
|3
|-
| rowspan="4" |Lobular Inflammation
|None
|0
|-
|<2 focci
|1
|-
|2-4
|2
|-
|>4
|3
|-
| rowspan="3" |Hepatocyte  Balloning
|None
|0
|-
|Few ballooned cells
|1
|-
|Many ballooned cells
|2
|-
| rowspan="3" style="background:#efefef;" |Interpretation
| style="background:#efefef;" |0-2
| style="background:#efefef;" |Non-diagnostic
|-
| style="background:#efefef;" |3-4
| style="background:#efefef;" |Borderline
|-
| style="background:#efefef;" |5-8
| style="background:#efefef;" |Diagnostic
|}
===Staging===
Based on the degree of fibrosis on biospy NASH can be classified into 4 stages.
{| border="1" cellpadding="5" cellspacing="0" align="center" |class="wikitable"
! colspan="2" style="background:#efefef;" |Staging
|-
|Stage 1
|
Zone 3 [[fibrosis]]<br>
Perisinusoidal fibrosis<br>
Portal/ periportal fibrosis
|-
|Stage 2
|Perisinusoidal and portal/periportal [[fibrosis]]
|-
|Stage 3
|Bridging [[fibrosis]]
|-
|Stage 4
|[[Cirrhosis]]
|}


==References==
==References==
{{reflist|2}}
{{reflist|2}}
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{{WS}}
[[Category:Gastroenterology]]
[[Category:Gastroenterology]]
[[Category:Hepatitis]]
[[Category:Hepatology]]
[[Category:Hepatology]]
[[Category:Disease]]
[[Category:Needs content]]
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Latest revision as of 16:23, 27 December 2017

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

Overview

Liver biopsy may be helpful in the diagnosis of non-alcoholic fatty liver disease. Findings on biopsy include macrovesicular steatosis, inflammation, ballooning degeneration, zone 3 perivenular/periportal/perisinusoidal fibrosis and, finally, mallory bodies.

Other Diagnostic Studies

  • Liver biopsy is considered as a gold-standard for diagnosing, grading, and staging NAFLD.
  • Invasive test
  • Associated with significant bleeding risk in patients with clotting abnormalities due to hepatic disease.

Complications

Complications of liver biopsy are rare but include

Findings

Classically, biopsy reveals:[1][2]

Interpretation

Histo-pathological classification

Depending on degree of steatosis, necroinflammatory activity, and degree of fibrosis non-alcoholic liver disease can be classified as follows:

Grading

NAFLD activity score is employed for grading steatohepatitis of NASH. NAS represents the sum of scores for steatosis, lobular inflammation, and ballooning.[4]

Component Range Score
Steatosis <5% 0
5-33% 1
34-66% 2
>66% 3
Lobular Inflammation None 0
<2 focci 1
2-4 2
>4 3
Hepatocyte Balloning None 0
Few ballooned cells 1
Many ballooned cells 2
Interpretation 0-2 Non-diagnostic
3-4 Borderline
5-8 Diagnostic

Staging

Based on the degree of fibrosis on biospy NASH can be classified into 4 stages.

Staging
Stage 1

Zone 3 fibrosis
Perisinusoidal fibrosis
Portal/ periportal fibrosis

Stage 2 Perisinusoidal and portal/periportal fibrosis
Stage 3 Bridging fibrosis
Stage 4 Cirrhosis

References

  1. Angula P. Nonalcoholic Fatty Liver Disease. NEJM. 2002 346(16):1221-31
  2. Brunt EM, Janney CG, Di Bisceglie AM et al. Nonalcoholic steatohepatitis: A proposal for grading and staging the histological lesions. Am. J. Gastroenterol. 1999; 94(9):2467-2474
  3. Skelly et al. Findings on liver biopsy to investigate abnormal liver function tests in the absence of diagnostic serology. J Hepatol 2001;35:195-9
  4. Vizuete J, Camero A, Malakouti M, Garapati K, Gutierrez J (2017). "Perspectives on Nonalcoholic Fatty Liver Disease: An Overview of Present and Future Therapies". J Clin Transl Hepatol. 5 (1): 67–75. doi:10.14218/JCTH.2016.00061. PMC 5411359. PMID 28507929.

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