Am J Cancer Res Ther | Volume 1, Issue 1 | Case Report | Open Access
Al Jeboury SA1*, Al Mazrooei H1 and Mahmood R2
1College of Medicine, Mohammad Bin Rashid University of Medicine and Health Sciences, Dubai, UAE 2Department of Oncology, Mediclinic City Hospital, Dubai, UAE
*Correspondance to: Sarah Ahmed Al Jeboury
Fulltext PDFPurpose: Vaginal cancer is a rare primary vaginal carcinoma. It accounts for only 1% to 2% of all gynecological malignancies. They arise as primary squamous cell cancers or as a result of extension from the cervix or vulva. Primary mucinous vaginal adenocarcinoma of intestinal-type is of an unknown histogenesis.
Methods and Materials: This report presents a case of a 29-year-old Para 0 woman with the complaint of a mass in the vagina and recurrent vaginal bleeding. She was evaluated and worked-up for examination under anesthesia and biopsy of the vaginal mass.
Results: The histological examination confirmed an intestinal-type variant of adenocarcinoma of the vagina.
Conclusion: Recognition of this rare entity is important, particularly to avoid the pitfall of misdiagnosing metastatic disease as primary vaginal cancer.
Al Jeboury SA, Al Mazrooei H, Mahmood R. Vaginal Adenocarcinoma of Intestinal-Type: A Case Report. Am J Cancer Res Ther. 2022; 1(1): 1004.