| Literature DB >> 34019237 |
Hussein Nassereddine1, Matthieu Chicaud2,3, Khedidja Rebah4, Nathalie Théou-Anton4, Anne Sautet5, Jacques Dermer6, Anne Couvelard2,7.
Abstract
Gastric type 1 neuroendocrine tumours are considered to have low rates of proliferation and a good prognosis. We report here a patient with an aggressive well-differentiated high-grade gastric neuroendocrine tumour (gastric grade 3 NET), in a context of autoimmune gastritis. Consistent with grade 3 disease, the tumour had a Ki-67 proliferation index of 30%. Targeted next-generation sequencing identified variants of four genes, including a pathogenic ATM variant underlying the differentiation and metastatic potential of the tumour. Liver metastasis was diagnosed during follow-up, and the patient died after 6 years, due to disease progression.Entities:
Keywords: Autoimmune gastritis; Gastric; Grade 3; Neuroendocrine tumour; Type 1
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Year: 2021 PMID: 34019237 DOI: 10.1007/s12022-021-09681-2
Source DB: PubMed Journal: Endocr Pathol ISSN: 1046-3976 Impact factor: 3.943