Primary retroperitoneal mucinous cystadenocarcinoma in a male patient
- 1Department of Pathology, National University of Singapore, Singapore, Republic of Singapore
- 2Department of Surgery, Tan Tock Seng Hospital, Singapore
- 3Department of Pathology, Singapore General Hospital, Singapore
- Correspondence to:
T P Thamboo
Department of Pathology, National University of Singapore, National University Hospital (Level 3), Lower Kent Ridge Road, Singapore 119074, Republic of Singapore;
- Accepted 3 June 2005
Primary retroperitoneal mucinous cystadenocarcinomas (PRMCs) are rare. This is the first reported case in the literature in English of PRMC in a man. The 64-year-old man presented with a large retroperitoneal cystic tumour measuring 24×20×16 cm3, which was removed intact. Areas ranging from a benign mucinous cyst to borderline mucinous tumour to mucinous cystadenocarcinoma were observed on microscopy. Strong patchy staining for cytokeratins 7 and 20 and strong diffuse staining for MUC2 and MUC5AC core peptides, similar to staining patterns in ovarian mucinous tumours, were shown in the benign and atypical epithelium. Staining for CA19.9 and carcinoembryonic antigen was also shown by both components. The theory of its origin from the mucinous metaplasia of peritoneal (mesothelial) inclusion cysts, rather than from ectopic ovarian tissue or ovarian teratomas, is supported by the occurrence of such a tumour in a male patient.
Competing interests: We declare that we have no financial or non-financial competing interests.