ENDOMETRIAL GASTRIC-TYPE ADENOCARCINOMA ARISING IN THE BACKGROUND OF MUCINOUS METAPLASIA: A CASE REPORT

Authors

  • Pongsada Prasonguppatum Institute of Pathology, Department of Medical Services, Ministry of Public Health

DOI:

https://doi.org/10.55374/jseamed.v9.246

Keywords:

endometrial gastric-type adenocarcinoma, endometrial gastric (gastrointestinal)-type mucinous lesion

Abstract

Endometrial gastric-type adenocarcinoma was recently included in the WHO Classification of Female Genital Tumors, 5th edition, as a very rare tumor. Some cases are linked to mucinous metaplasia, and histologic grade does not correlate with prognosis. Currently, there is no standard treatment available. This report describes a 70-year-old female patient who presented with leukorrhea. An endometrial biopsy revealed atypical mucinous glands and a positive result of p16, initially diagnosed as cervical adenocarcinoma. However, after a hysterectomy, a polypoid mass was identified in the endometrial cavity, leading to a revised diagnosis of endometrial gastric-type adenocarcinoma associated with mucinous metaplasia. Immunohistochemical staining showed positive results for CK20, CDX2, and MUC6 in the mucinous metaplasia region, whereas MUC6 was negative in the adenocarcinoma. The tumor was confined to the endometrium with no invasion or spread to lymph nodes. One-year postoperative follow-up showed no recurrence. This cancer is rare and has histological features that overlap with other tumors, underscoring the importance of differential diagnosis for accurate identification.

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References

Wong RWC, Ralte A, Grondin K, Talia KL, McCluggage WG. Endometrial gastric (gastrointestinal)-type mucinous lesions: report of a series illustrating the spectrum of benign and malignant lesions. Am J Surg Pathol 2020; 44: 406-19. DOI: https://doi.org/10.1097/PAS.0000000000001381

Bragantini E, Angelico G, Disanto MG, Magri E, Maccio L, Barbareschi M. Gastric (gastrointestinal)-type endometrial adenocarcinoma presenting as a solitary endometrial polyp: a case report and literature review on a novel and potentially aggressive endometrial cancer histotype. Pathologica. 2023; 115: 227. DOI: https://doi.org/10.32074/1591-951X-870

Wong RW, Talia KL, McCluggage WG. Endometrial gastric-type carcinoma: an aggressive and morphologically heterogenous new histotype arising from gastric metaplasia of the endometrium. Am J Surg Pathol 2020; 44: 1736-37. DOI: https://doi.org/10.1097/PAS.0000000000001473

Travaglino A, Raffone A, Gencarelli A, Mollo A, Zullo F, Insabato L. Endometrial gastric-type carcinoma: an aggressive and morphologically heterogenous new histotype arising from gastric metaplasia of the endometrium. Am J Surg Pathol 2020; 44: 1002-4. DOI: https://doi.org/10.1097/PAS.0000000000001474

Mangili G, Taccagni G, Garavaglia E, Carnelli M, Montoli S. An unusual admixture of neoplastic and metaplastic lesions of the female genital tract in the Peutz-Jeghers Syndrome. Gynecol Oncol 2004; 92: 337–42. DOI: https://doi.org/10.1016/j.ygyno.2003.10.005

Zhou Y, Wang X, Li Y, Zhang W, Xu X, Pang Y, et al. When synchronous mucinous metaplasia and neoplasia of the female genital tract and Peutz-Jeghers syndrome meet: a case report and literature review. BMC Womens Health 2024; 24: 375. DOI: https://doi.org/10.1186/s12905-024-03184-y

Carleton C, Hoang L, Sah S, Kiyokawa T, Karamurzin YS, Talia KL, et al. A Detailed immunohistochemical analysis of a large series of cervical and vaginal gastric-type adenocarcinomas. Am J Surg Pathol 2016; 40: 636–44. DOI: https://doi.org/10.1097/PAS.0000000000000578

endometrial gastric-type adenocarcinoma characterized by complex glandular growth

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Published

2025-09-11

How to Cite

1.
Prasonguppatum P. ENDOMETRIAL GASTRIC-TYPE ADENOCARCINOMA ARISING IN THE BACKGROUND OF MUCINOUS METAPLASIA: A CASE REPORT. J Southeast Asian Med Res [Internet]. 2025 Sep. 11 [cited 2025 Sep. 12];9:e0246. Available from: https://www.jseamed.org/index.php/jseamed/article/view/246

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Section

Case Reports