Tomioka Masayuki, Nakane Keita, Iinuma Koji, Kawase Kota, Taniguchi Tomoki, Tobisawa Yuki, Muto Aoi, Kanayama Tomohiro, Miyazaki Tatsuhiko, Koie Takuya
Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Department of Pathology, Gifu University Hospital, Gifu 5011194, Japan.
Curr Oncol. 2025 Sep 5;32(9):500. doi: 10.3390/curroncol32090500.
Primary retroperitoneal mucinous cystadenocarcinoma (PRMC) is an uncommon malignant neoplasm with few reported cases, particularly among male patients. Currently, only nine documented cases have been reported worldwide, including the present case. The present case report describes the incidental detection of PRMC in an 86-year-old male patient. Despite being offered surgical intervention, the patient initially opted against treatment. Consequently, follow-up imaging examinations were performed for 3 subsequent years. The tumor, initially measuring 31 × 32 × 31 mm, gradually increased to 58 × 60 × 59 mm. Subsequently, the patient underwent laparoscopic retroperitoneal tumor resection. Histopathological examination revealed adenocarcinoma characterized by intestinal differentiation. The patient has exhibited no evidence of disease for 1 year postoperatively. The present case is noteworthy, as this disease rarely occurs in men, thereby offering significant potential for educational and scientific contributions. Notably, the patient's age, longitudinal observation of tumor progression through imaging over a period of 3 years, and complete surgical excision of the tumor are salient features of this case. These findings may prove useful in the diagnosis and treatment strategy for male patients with PRMC.
原发性腹膜后黏液性囊腺癌(PRMC)是一种罕见的恶性肿瘤,报道的病例较少,尤其是男性患者。目前,全球仅报道了9例有记录的病例,包括本病例。本病例报告描述了一名86岁男性患者偶然发现PRMC的情况。尽管提供了手术干预,但患者最初选择不接受治疗。因此,在随后的3年里进行了随访影像学检查。肿瘤最初大小为31×32×31mm,逐渐增大至58×60×59mm。随后,患者接受了腹腔镜腹膜后肿瘤切除术。组织病理学检查显示为具有肠化生特征的腺癌。患者术后1年无疾病迹象。本病例值得关注,因为这种疾病很少发生在男性身上,因此具有重要的教育和科学贡献潜力。值得注意的是,患者的年龄、通过影像学对肿瘤进展进行3年的纵向观察以及肿瘤的完整手术切除是本病例的显著特征。这些发现可能对男性PRMC患者的诊断和治疗策略有用。