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EDITORIAL  
Year : 2021  |  Volume : 64  |  Issue : 5  |  Page : 4-5
Evolving significance of liver pathology


Department of Pathology, GB Pant Institute of Postgraduate Medical Education and Research, New Delhi, India

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Date of Submission08-Apr-2021
Date of Decision10-Apr-2021
Date of Acceptance28-May-2021
Date of Web Publication7-Jun-2021
 

How to cite this article:
Sakhuja P. Evolving significance of liver pathology. Indian J Pathol Microbiol 2021;64, Suppl S1:4-5

How to cite this URL:
Sakhuja P. Evolving significance of liver pathology. Indian J Pathol Microbiol [serial online] 2021 [cited 2021 Jun 14];64, Suppl S1:4-5. Available from: https://www.ijpmonline.org/text.asp?2021/64/5/4/317911




Liver pathology has two main elements: nonneoplastic and neoplastic. These elements also remain linked as primary liver tumors are often a consequence of a preexisting liver disease. Role of liver biopsy in the current era of newer imaging modalities has undergone a sea change in the last few decades.[1] Initially, a large number of biopsies were from patients with viral hepatitis, for grading of activity and staging of fibrosis.[2] This was overtaken by biopsies for confirming the diagnosis of Nonalcoholic Steatohepatitis (NASH) and its grading and staging. While liver biopsy for NASH is still common in several centers, biopsies for viral hepatitis are done occasionally as the viral load along with the liver enzymes are more useful to guide therapy. Often the role of the pathologist is to confirm a clinical diagnosis especially where the clinical data are conflicting, or to detect any unsuspected disease or comorbidity. In addition, the liver biopsy helps guide treatment decisions based on the predominant histological features.

The role of liver biopsy in the diagnosis of metabolic and cholestatic disorders in pediatric patients as well as adults must be emphasized as genetic advancements and newer immunohistochemistry (IHC) markers are offering new perspectives and therapeutic avenues to such patients. Liver biopsy continues to play an important role in the diagnosis, prognosis, and management of patients with genetic disorders like hemochromatosis, Wilson's disease, progressive familial intrahepatic cholestasis (PFIC), and storage disorders.

The end result of chronic liver disease is fibrosis of varying stages finally culminating in cirrhosis. Thus, the role of the pathologist is not only to quantify the degree of fibrosis, but also to assess the regression of fibrosis, the thickness of fibrous septa, and architectural changes which can predict response to antifibrotic therapies and thus prognosis. Several grading and staging systems have been proposed for both viral hepatitis and NASH.[2],[3],[4] Liver biopsy versus noninvasive methods of assessing fibrosis in the liver has been a subject of many a debate.[5] However, newer techniques such as second-harmonic generation and two-photon microscopy have provided greater reliability for fibrosis and steatosis assessment.[6],[7]

Diagnosis of liver space-occupying lesion (SOL) is another area where the Pathologist plays a key role, especially in situations wherein the radiology is not conclusive. In such situations, a biopsy may be required to differentiate between hepatocellular carcinoma (HCC) and an adenoma or focal nodular hyperplasia in a noncirrhotic liver, or from a dysplastic nodule in a cirrhotic liver. IHC and molecular studies have improved our insight into the pathogenesis and categorization of prognostically distinct subtypes of hepatic adenomas. This helps identify those with a higher risk for progression to malignancy. With the advent of surrogate IHC markers, the pathologist must be able to diagnose and subclassify the phenotypic and molecular subtype of HCC as this may impact treatment and prognosis. IHC plays a key role not only in diagnosis but also in subtyping for the purpose of molecular classification and prognostication. In the latter, role antibodies such as p53 and beta-catenin, etc., are useful. With the era of predictive and precision medicine, and the role of targeted therapy, such information provided by the pathologist is vital.[1]

Improvement in surgical techniques have increased the number of liver resections and liver transplants for varying etiologies. It is important for the pathologist to appropriately gross the liver resection specimen in order to provide the pertinent information required. Furthermore, post-transplant liver biopsies are often done in graft dysfunction to assess the type of rejection and to distinguish it from drug-induced liver injury, acute hepatitis due to opportunistic viral infections, de novo disease or recurrence of the primary disease. Liver biopsy has also been useful in guiding the diagnostic criteria for antibody-mediated rejection in the liver.[8]

To conclude, the indications for liver biopsy and the role of the pathologist in liver biopsy interpretation has seen a lot of changes in the past few decades. Currently, the role is (a) to confirm a clinical diagnosis such as NASH, Autoimmune liver disease and look for any co-morbidity, (b) estimation of liver fibrosis, (c) diagnosis and categorization of liver SOL, (d) phenotypic and molecular classification of HCC, (e) assessment of post-transplant biopsies, etc., to name a few. Liver Pathology continues to improve patient care by guiding diagnosis and therapy and is an important complementary tool in clinical research trials.



 
   References Top

1.
Torbenson M, Washington K. Pathology of liver disease: Advances in the last 50 years. Hum Pathol 2020;95:78-98.  Back to cited text no. 1
    
2.
Goodman ZD. Grading and staging systems for inflammation and fibrosis in chronic liver diseases. J Hepatol 2007;47:598-607.  Back to cited text no. 2
    
3.
Kleiner DE, Brunt EM, Van Natta M, Behling C, Contos MJ, Cummings OW, et al. Design and validation of a histological scoring system for nonalcoholic fatty liver disease. Hepatology 2005;41:1313-21.  Back to cited text no. 3
    
4.
Bedossa P. Diagnosis of non-alcoholic fatty liver disease/non-alcoholic steatohepatitis: Why liver biopsy is essential. Liver Int 2018;38(Suppl 1):64-6.  Back to cited text no. 4
    
5.
Xiao G, Zhu S, Xiao X, Yan L, Yang J, Wu G. Comparison of laboratory tests, ultrasound, or magnetic resonance elastography to detect fibrosis in patients with nonalcoholic fatty liver disease: A meta-analysis. Hepatology 2017;66:1486-501.  Back to cited text no. 5
    
6.
Tai DC, Tan N, Xu S, Kang CH, Chia SM, Cheng CL, et al. Fibro-C-Index: Comprehensive, morphology-based quantification of liver fibrosis using second harmonic generation and two-photon microscopy. J Biomed Opt 2009;14:044013.  Back to cited text no. 6
    
7.
Liu F, Goh GB, Tiniakos D, Wee A, Leow WQ, Zhao JM, et al. qFIBS: An automated technique for quantitative evaluation of fibrosis, inflammation, ballooning, and steatosis in patients with nonalcoholic steatohepatitis. Hepatology 2020;71:1953-66.  Back to cited text no. 7
    
8.
Demetris AJ, Bellamy C, Hübscher SG, O'Leary J, Feng S, et al. 2016 Comprehensive update of the banff working group on liver allograft pathology: Introduction of antibody-mediated rejection. Am J Transplant 2016;16:2816-35.  Back to cited text no. 8
    

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Correspondence Address:
Puja Sakhuja
Department of Pathology, GB Pant Institute of Postgraduate Medical Education and Research, New Delhi
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijpm.ijpm_363_21

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