BMJ Case Reports | 2021

Complete pelvic organ prolapse associated with cervical cancer

 
 
 
 

Abstract


© BMJ Publishing Group Limited 2021. No commercial reuse. See rights and permissions. Published by BMJ. DESCRIPTION Pelvic organ prolapse and carcinoma of the cervix are common entities but their association is rare. In more than 60% of the cases, the uterine prolapse is present for at least 10 years. The displacement of the uterine cervix from the natural environment of the vagina is thought to explain a lower risk of cervical cancer due to viral infection in uterine prolapse. Nevertheless, the continuous injury of the cervical epithelium may favour the neoplastic process. The best treatment approach in this clinical setting is not clearly defined and vary considerably among authors. We present a case of a 74yearold woman, Gesta 3 Para 3, with a 9 years history of an uterine prolapse that presented in our department. The reasons for medical visit were the onset of vaginal bleeding and increasing genital prolapse size. The patient had no prior cervical cancer screening. Physical examination revealed a complete and irreducible fourthdegree urogenital prolapse with induration of the entire vaginal mucosa, inflammatory signs and ulcerated lesions that made impossible to clearly identify the cervix (figure 1). No evidence of bladder or rectum involvement were present. Biopsies were performed and histopathology revealed squamouscell cervical carcinoma. A pelvic MRI described a fibromatous uterus measuring 15×7, 8×10 cm, large ptosis of the uterus and bladder, bilateral parametrial invasion and hydronephrosis (figure 2). CT of the thorax and abdomen revealed no distant metastasis. She was staged according to the 2009 International Federation of Gynecology and Obstetrics staging system as at least FIGO IIIA. Radiotherapy was considered but the risk of visceral injury was high due to the volume of externalised prolapse and associated cystocele. After

Volume 14
Pages None
DOI 10.1136/bcr-2020-239706
Language English
Journal BMJ Case Reports

Full Text