Vulvar Villoglandular Adenocarcinoma of Colonic Type: A Rare Finding
(ندگان)پدیدآور
Esmaeili, HeidaraliAzimpouran, MahzadOlad-Saheb-Madarek, Elahehنوع مدرک
TextCase Report
زبان مدرک
Englishچکیده
Colonic type villoglandular adenocarcinoma of the lower genital tract is an extremely rare condition. Its origin is not clearly understood; however, the cloacal remnants are the more accepted source for this carcinoma.We report the case of a 67-year-old female patient who presented with a 1.2 cm polypoidal nodule at the right side of the fourchette. Morphologic studies revealed a colonic type mucinous adenocarcinoma that arose from within a villous adenoma. Immunohistochemical staining showed positive cytokeratin 7, cytokeratin 20, carcinoembryonic antigen, P53, and progesterone receptor, but negative for estrogen receptor and caudal type homeobox transcription factor 2. Extensive work-up failed to reveal other primary cancers in this patient. Ultimately, she underwent a radical vulvectomy. No recurrence was seen in eight months follow up of this patient after surgery. Careful, thorough histological evaluation and clinical clues enable correct diagnosis of the rare colonic type vulvar villoglandular adenocarcinoma. Due to rarity of this tumor, its management is questionable. Therefore, additional investigation is necessary for its management.
شماره نشریه
1تاریخ نشر
2018-01-011396-10-11
ناشر
Shiraz University of Medical Sciencesسازمان پدید آورنده
Department of General Pathology, Tabriz University of Medical Sciences, Tabriz, IranDepartment of General Pathology, Tabriz University of Medical Sciences, Tabriz, Iran
Department of Obstetrics and Gynecology, Tabriz University of Medical Sciences, Tabriz, Iran
شاپا
2008-67092008-6687