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Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases
Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases
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Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases
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Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases
Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases

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Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases
Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases
Journal Article

Pathological features of gastric‑type endocervical adenocarcinoma: A report of two cases

2024
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Overview
Gastric-type endocervical adenocarcinoma (GEA) is an uncommon form of uterine cervical adenocarcinoma with an unfavorable prognosis. The tumor consists of glands exhibiting a morphological resemblance to gastric cells and occasionally manifests features akin to pancreaticobiliary mucinous adenocarcinoma. GEA differs from the typical cervical cancer, particularly in its lack of association with the human papillomavirus. Immunophenotypic analysis suggests intestinal differentiation. The present study reports two cases of GEA occurring in postmenopausal individuals who were diagnosed in Lishui Central Hospital (Lishui, China) between January 2015 and January 2023. Microscopic examination revealed cysts lined with mucinous cells within the tumors. Immunohistochemical assays confirmed the positivity of the tumors for cytokeratin 7, mucin (MUC)5AC, and mutant tumor protein p53, while the results were negative for tumor suppressor p16, and in one case for paired box protein 8, consistent with characteristics of mucinous adenocarcinoma originating from the gastrointestinal tract. Programmed death-ligand 1 expression was also negative. The proto-oncogene K-ras was identified using amplification refractory mutation system polymerase chain reaction. Both cases were negative for mutations in codons 12 and 13 of exon 2, codon 61 of exon 3 and codon 146 of exon 4, but were positive for wild-type K-ras. Clinical follow-up revealed a potential association between histopathological features and resistance to chemotherapeutic drugs. The infrequency of this tumor type may contribute to diagnostic challenges.