Hepatocellular carcinoma: Clinicopathologic associations amidst marked phenotypic heterogeneity.


Journal

Pathology, research and practice
ISSN: 1618-0631
Titre abrégé: Pathol Res Pract
Pays: Germany
ID NLM: 7806109

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 13 09 2020
revised: 08 11 2020
accepted: 10 11 2020
pubmed: 12 12 2020
medline: 13 10 2021
entrez: 11 12 2020
Statut: ppublish

Résumé

Hepatocellular carcinoma (HCC) is characterized by marked phenotypic and molecular heterogeneity. Clinico-morphologic phenotypes and associations are important surrogate markers of molecular aberrations; therefore have immense relevance for targeted therapy. There is paucity of published literature on critical analysis of HCC heterogeneity and morphological alliance. To assess the heterogeneity and dominance of histomorphological features, and to explore clinicopathological associations in HCC. Retrospective cross-sectional study of 217 HCC tissue specimens was performed for the assessment of prevalence of major histological patterns, cytological features, and clinicopathological correlation. Homogeneous architecture with a single dominant histological pattern was a rarity. Single pattern constituting ≥50 % of the tumour was found in less than 1/5th of the cases. Macrotrabecular HCC represented 9.2 % of cases. The simultaneous presence of 2-3 patterns or atypical variants and/ or cytological characteristics was recorded in 25 % and 30 % respectively. Significant clinicopathological associations: Pseudoglandular with microtrabecular pattern-cholestasis, showed better differentiation and early-stage; macrotrabecular pattern frequently occurred with pleomorphic giant cells, higher tumour stage, higher AFP levels; solid pattern often showed clear cells. Noticeable mutual exclusions were MD bodies with microtrabecular and pseudoglandular patterns; Compact pattern with neutrophilic clusters and cholestasis. Larger tumours were significantly more heterogeneous; however, heterogeneity did not correlate with outcome CONCLUSIONS: HCC displays immense heterogeneity with an amalgamation of different histomorphological patterns and features; nevertheless, there are certain reproducible associations and omissions. Tumor biopsies agree fairly well with large specimens. Characterization of phenotypic heterogeneity, dominance, associations, and exclusions in individual patients provides vital information.

Sections du résumé

BACKGROUND BACKGROUND
Hepatocellular carcinoma (HCC) is characterized by marked phenotypic and molecular heterogeneity. Clinico-morphologic phenotypes and associations are important surrogate markers of molecular aberrations; therefore have immense relevance for targeted therapy. There is paucity of published literature on critical analysis of HCC heterogeneity and morphological alliance.
AIMS OBJECTIVE
To assess the heterogeneity and dominance of histomorphological features, and to explore clinicopathological associations in HCC.
METHODS METHODS
Retrospective cross-sectional study of 217 HCC tissue specimens was performed for the assessment of prevalence of major histological patterns, cytological features, and clinicopathological correlation.
RESULTS RESULTS
Homogeneous architecture with a single dominant histological pattern was a rarity. Single pattern constituting ≥50 % of the tumour was found in less than 1/5th of the cases. Macrotrabecular HCC represented 9.2 % of cases. The simultaneous presence of 2-3 patterns or atypical variants and/ or cytological characteristics was recorded in 25 % and 30 % respectively. Significant clinicopathological associations: Pseudoglandular with microtrabecular pattern-cholestasis, showed better differentiation and early-stage; macrotrabecular pattern frequently occurred with pleomorphic giant cells, higher tumour stage, higher AFP levels; solid pattern often showed clear cells. Noticeable mutual exclusions were MD bodies with microtrabecular and pseudoglandular patterns; Compact pattern with neutrophilic clusters and cholestasis. Larger tumours were significantly more heterogeneous; however, heterogeneity did not correlate with outcome CONCLUSIONS: HCC displays immense heterogeneity with an amalgamation of different histomorphological patterns and features; nevertheless, there are certain reproducible associations and omissions. Tumor biopsies agree fairly well with large specimens. Characterization of phenotypic heterogeneity, dominance, associations, and exclusions in individual patients provides vital information.

Identifiants

pubmed: 33307344
pii: S0344-0338(20)32145-2
doi: 10.1016/j.prp.2020.153290
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

153290

Informations de copyright

Copyright © 2020 Elsevier GmbH. All rights reserved.

Auteurs

Archana Rastogi (A)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: drarchanarastogi@gmail.com.

Rakhi Maiwall (R)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: rakhi_2011@yahoo.co.in.

Gayatri Ramakrishna (G)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: gayatrirama1@gmail.com.

Shilpi Modi (S)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: drshilpi.modi@gmail.com.

Kanika Taneja (K)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: drkanikataneja09@gmail.com.

Chhagan Bihari (C)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: drcbsharma@gmail.com.

Guresh Kumar (G)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: chibbegk@gmail.com.

Nilesh Patil (N)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: dr.nils.p@gmail.com.

Shalini Thapar (S)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: thaparshalini@gmail.com.

Ashok Kumar Choudhury (AK)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: doctor.ashokchoudhury@gmail.com.

Amar Mukund (A)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: dramarmukund@gmail.com.

Viniyendra Pamecha (V)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India.

Shiv K Sarin (SK)

Institute of Liver & Biliary Sciences, D-1 Vasant Kunj, Delhi, 110070, India. Electronic address: shivsarin@gmail.com.

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