TY - JOUR
T1 - Hepatocellular adenoma in men
T2 - A nationwide assessment of pathology and correlation with clinical course
AU - Dutch Benign Liver Tumor Grp
AU - PALGA Grp
AU - van Rosmalen, Belle V.
AU - Furumaya, Alicia
AU - Klompenhouwer, Anne J.
AU - Tushuizen, Maarten E.
AU - Braat, Andries E.
AU - Reinten, Roy J.
AU - Ligthart, Marjolein A. P.
AU - Haring, Martijn P. D.
AU - de Meijer, Vincent E.
AU - van Voorthuizen, Theo
AU - Takkenberg, R. Bart
AU - Dejong, Cornelis H. C.
AU - de Man, Robert A.
AU - IJzermans, Jan N. M.
AU - Doukas, Michail
AU - van Gulik, Thomas M.
AU - Verheij, Joanne
N1 - This article is protected by copyright. All rights reserved.
PY - 2021/10
Y1 - 2021/10
N2 - BACKGROUND & AIMS: Hepatocellular adenomas (HCA) rarely occur in males, and if so, are frequently associated with malignant transformation. Guidelines are based on small numbers of patients and advise resection of HCA in male patients, irrespective of size or subtype. This nationwide retrospective cohort study is the largest series of HCA in men correlating (immuno)histopathological and molecular findings with the clinical course.METHODS: Dutch male patients with available histological slides with a (differential) diagnosis of HCA between 2000 and 2017 were identified through the Dutch Pathology Registry (PALGA). Histopathology and immunohistochemistry according to international guidelines were revised by two expert hepatopathologists. Next generation sequencing (NGS) was performed to confirm hepatocellular carcinoma (HCC) and/or subtype HCA. Final pathological diagnosis was correlated with recurrence, metastasis and death.RESULTS: A total of 66 patients from 26 centers fulfilling the inclusion criteria with a mean (±SD) age of 45.0±21.6 years were included. The diagnosis was changed after expert revision and NGS in 33 of the 66 patients (50%). After a median follow-up of 9.6 years, tumor-related mortality of patients with accessible clinical data was 1/18 (5.6%) in HCA, 5/14 (35.7%) in uncertain HCA/HCC and 4/9 (44.4%) in the HCC groups (p=0.031). Four B-catenin mutated HCA were identified using NGS, which were not yet identified by immunohistochemistry and expert revision.CONCLUSIONS: Expert revision with relevant immunohistochemistry may help the challenging but prognostically relevant distinction between HCA and well-differentiated HCC in male patients. NGS may be more important to subtype HCA than indicated in present guidelines.
AB - BACKGROUND & AIMS: Hepatocellular adenomas (HCA) rarely occur in males, and if so, are frequently associated with malignant transformation. Guidelines are based on small numbers of patients and advise resection of HCA in male patients, irrespective of size or subtype. This nationwide retrospective cohort study is the largest series of HCA in men correlating (immuno)histopathological and molecular findings with the clinical course.METHODS: Dutch male patients with available histological slides with a (differential) diagnosis of HCA between 2000 and 2017 were identified through the Dutch Pathology Registry (PALGA). Histopathology and immunohistochemistry according to international guidelines were revised by two expert hepatopathologists. Next generation sequencing (NGS) was performed to confirm hepatocellular carcinoma (HCC) and/or subtype HCA. Final pathological diagnosis was correlated with recurrence, metastasis and death.RESULTS: A total of 66 patients from 26 centers fulfilling the inclusion criteria with a mean (±SD) age of 45.0±21.6 years were included. The diagnosis was changed after expert revision and NGS in 33 of the 66 patients (50%). After a median follow-up of 9.6 years, tumor-related mortality of patients with accessible clinical data was 1/18 (5.6%) in HCA, 5/14 (35.7%) in uncertain HCA/HCC and 4/9 (44.4%) in the HCC groups (p=0.031). Four B-catenin mutated HCA were identified using NGS, which were not yet identified by immunohistochemistry and expert revision.CONCLUSIONS: Expert revision with relevant immunohistochemistry may help the challenging but prognostically relevant distinction between HCA and well-differentiated HCC in male patients. NGS may be more important to subtype HCA than indicated in present guidelines.
KW - high-throughput nucleotide sequencing
KW - immunohistochemistry
KW - liver cell adenoma
KW - male
KW - MALIGNANT POTENTIAL PROPOSAL
KW - MOLECULAR CLASSIFICATION
KW - GLUTAMINE-SYNTHETASE
KW - LIVER BIOPSIES
KW - NEOPLASM
KW - MUTATIONS
KW - CARCINOMA
KW - TUMORS
KW - TRANSFORMATION
KW - DIAGNOSIS
U2 - 10.1111/liv.14989
DO - 10.1111/liv.14989
M3 - Article
C2 - 34155783
SN - 1478-3223
VL - 41
SP - 2474
EP - 2484
JO - Liver International
JF - Liver International
IS - 10
ER -