α-Fetoprotein-Producing Hepatoid Gastric Adenocarcinoma With Osteoclast-Like Giant Cells and Neuroendocrine Differentiation

Author:

Wincewicz Andrzej12,Kowalik Artur3,Zięba Sebastian3,Lewitowicz Piotr24,Góźdź Stanisław56,Sulkowski Stanisław7

Affiliation:

1. Department of Anatomy, Faculty of Health Sciences, Jan Kochanowski University, Kielce, Poland

2. Non Public Health Care Unit - Department of Pathology, Kielce, Poland, Specialist Medical Practice-Pathologist Kielce

3. Department of Molecular Diagnostics, Holy Cross Cancer Center, Kielce, Poland

4. Department of Pathology, Faculty of Health Sciences, Jan Kochanowski University of Kielce

5. Department of Clinical Oncology Holy Cross Cancer Centre, Kielce, Poland

6. Department of Prevention and Epidemiology of Neoplasms, Institute of Public Health, Faculty of Health Sciences, Jan Kochanowski University, Poland

7. Department of General Pathomorphology, Collegium Pathologicum, Medical University of Bialystok, Poland

Abstract

Here we present the case of a 73-year-old woman with an ulcerated, advanced, hepatoid, and α-fetoprotein-producing poorly differentiated (G3) primary gastric adenocarcinoma pT3 N3a M1 with multinucleated cells and evident neuroendocrine component. This tumor was consistent with giant cell tumor type gastric carcinoma with osteoclast-like giant cells (OGCs). The cancer was HER2 and E-cadherin negative, chromogranin A dispersedly and moderately positive, and strongly α-fetoprotein-positive with evident CK AE1/AE3 immunoreactivity, while OGCs expressed CD68. To provide an insight into the molecular background of this peculiar neoplasm, next-generation sequencing (NGS) was performed to analyze the 50 most frequently mutated oncogenes and tumor suppressors. We detected mutations in the primary tumor in the following genes: KIT, EGFR, PTEN, ATM, and RB1. In the liver metastasis, we revealed mutations in 3 genes: PIK3CA, KIT, and CDKN2A.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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