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Fetal-type gastrointestinal adenocarcinoma: a morphologically distinct entity with unfavourable prognosis.
- Source :
-
Journal of clinical pathology [J Clin Pathol] 2018 Mar; Vol. 71 (3), pp. 221-227. Date of Electronic Publication: 2017 Aug 16. - Publication Year :
- 2018
-
Abstract
- Aims: This multi-institutional study and a re-evaluation of the TCGA cohort explores the morphological spectrum, genetics and outcome of GI (gastrointestinal) hepatoid tumours, tumours expressing alpha-fetoprotein (AFP) and fetal-type (FT) GI adenocarcinomas.<br />Methods: 44 tumours with evidence of hepatocellular differentiation were evaluated for morphology as well as by immunohistochemistry for AFP, HepPar1, glypican-3 and arginase-1 and by in situ hybridisation for albumin. Three categories were defined: type I (hepatoid: morphological evidence of hepatocellular differentiation), type II (FT GI adenocarcinoma: tubular profiles and subnuclear vacuolisation, resembling fetal intestine) and type III: positive for at least two hepatocyte-specific markers but lacking morphological evidence of hepatocellular differentiation. GI adenocarcinomas in the TCGA cohort were also evaluated (n=829).<br />Results: 18 cases were classified as type I, 19 as FT GI adenocarcinomas and 7 as type III (resembling conventional gastrointestinal carcinomas). Serum AFP was elevated in 92% of cases. 93% of tumours were positive for glypican-3, 90% for albumin and 89% for AFP. Arginase-1 was restricted to 35% of type 1 tumours. TCGA gastric tumours with elevated AFP expression showed morphological features of FT GI adenocarcinoma (70%) and were exclusively MSI stable. TCGA gastric adenocarcinomas with high AFP expression showed inferior survival on univariate and multivariate analysis.<br />Conclusions: FT GI adenocarcinomas show a distinctive morphological and immunohistochemical profile. Gastric adenocarcinomas with elevated expression of AFP morphologically resemble FT GI adenocarcinomas, demonstrate aggressive behaviour, independent of grade and stage, and a distinct genetic profile.<br />Competing Interests: Competing interests: The work was partially funded by a sponsored research agreement between the authors’ institution and Affymetrix, California, USA.<br /> (© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.)
- Subjects :
- Adenocarcinoma diagnosis
Adenocarcinoma pathology
Adult
Aged
Aged, 80 and over
Carcinoma, Hepatocellular diagnosis
Carcinoma, Hepatocellular pathology
Cohort Studies
Female
Gastrointestinal Neoplasms diagnosis
Gastrointestinal Neoplasms pathology
Hepatocytes pathology
Humans
Immunohistochemistry
In Situ Hybridization
Liver Neoplasms diagnosis
Liver Neoplasms pathology
Male
Middle Aged
Prognosis
Adenocarcinoma classification
Biomarkers, Tumor analysis
Carcinoma, Hepatocellular classification
Gastrointestinal Neoplasms classification
Liver Neoplasms classification
Subjects
Details
- Language :
- English
- ISSN :
- 1472-4146
- Volume :
- 71
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of clinical pathology
- Publication Type :
- Academic Journal
- Accession number :
- 28814568
- Full Text :
- https://doi.org/10.1136/jclinpath-2017-204535