Dede Murat, Deveci Güzin, Deveci M Salih, Yenen Mufit Cemal, Goktolga Umit, Dilek Saffet, Gunhan Omer
Department of Obstetric and Gynecology, Gulhane Military Medical Academy, Ankara, Turkey.
Tohoku J Exp Med. 2004 Apr;202(4):305-10. doi: 10.1620/tjem.202.305.
Villoglandular papillary adenocarcinoma (VPA) of cervix is rare but a well recognized variant of cervical adenocarcinoma with favorable prognosis occurring in younger age group. A 28-year-old white woman, gravida 3, para 2 was admitted for abnormal vaginal bleeding, when she was pregnant at 8th weeks of gestation. Physical examination revealed about 2.5 cm polipoid lesion of the cervix protruding into vagina. Histopathological findings were consistent with cervical VPA. After termination of pregnancy, radical hysterectomy type III was performed. The patient underwent second, third and fourth laparotomies because of recurrent pelvic masses. At the end of five years follow-up period, she died because of the complication of recurrent tumor. VPA is not an innocent tumor, and can be complicated by recurrence and metastasis. More radical surgical and medical attempts should be planned.