Abstract
We present the case of a 32-year-old woman with a previous surgical history of benign mucinous cystadenoma resected in 2012 who underwent magnetic resonance cholangiopancreatography following her second pregnancy in 2020. This demonstrated a large cystic mass in the left subdiaphragmatic space. Histopathology confirmed a well-differentiated primary peritoneal mucinous cystadenocarcinoma displaying cells of a Mullerian origin. We subsequently discuss the aetiology of these conditions separately and explore the possibility of a connection between the two regarding origin or potential malignant transformation that may otherwise have occurred coincidentally in this young patient. We also acknowledge a paucity of evidence regarding subsequent management strategies.
Reference12 articles.
1. Adenocarcinoma of Mullerian origin: review of pathogenesis, molecular biology, and emerging treatment paradigms;Cobb;Gynecol Oncol Res Pract,2015
2. Histologic pattern, bilaterality and clinical evaluation of 957 ovarian neoplasms: a 10-year study in a tertiary hospital of eastern India;Mondal;J Cancer Res Ther,2011
3. Primary retroperitoneal mucinous cystadenoma;Lee;Ann Coloproctol,2016
4. Wang CY , Rogers T , Katherine WS . Primary peritoneal mucinous adenocarcinoma: rarest of the rare? Open J Clin Med Case Rep 2018;1361.
5. Ovarian cancer, the revised FIGO staging system, and the role of imaging;Javadi;AJR Am J Roentgenol,2016
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献