Takasi M, Murase T, Narita H, Miyake K, Mitsuya H, Takatsuki K, Tsubone M, Nakashima N
Hinyokika Kiyo. 1985 Mar;31(3):499-506.
A case of primary adenocarcinoma of the urinary bladder occurring in a patient with type 1 multiple endocrine adenomatosis (MEA) is presented. The patient was a 36-year-old female who had a past history of type 1 multiple endocrine adenomatosis, namely, adenomatosis of the parathyroid gland, insulin and gastrin-producing adenomatosis of the pancreas, and prolactin-producing pituitary adenoma. She was admitted in January 1981 with the complaints of gross hematuria, pollakisuria and micturition pain lasting for about one year and a half. Cystoscopic examination revealed four solid tumors in the posterior and left lateral walls of the bladder with diffuse mucosal hyperemia. Biopsy of the tumors disclosed that they were adenocarcinoma. Clinical examinations revealed that there was no extravesical primary malignant neoplasm in this case. Radical cystectomy with urinary diversion by ileal conduit was performed on January 22, 1981. Histological examination revealed that the tumor was adenocarcinoma originating from the vesical mucosa. Follow-up for over three years since the time of surgery has not shown any sign of tumor recurrence or occurrence of extravesical malignant neoplasm. In addition, 28 cases of primary adenocarcinoma of urinary bladder in Japan reported during the last 25 years are reviewed and analyzed.
本文报告1例1型多发性内分泌腺瘤病(MEA)患者发生的原发性膀胱腺癌。患者为36岁女性,既往有1型多发性内分泌腺瘤病病史,即甲状旁腺腺瘤病、胰腺胰岛素和胃泌素生成腺瘤病以及催乳素生成垂体腺瘤。1981年1月,她因肉眼血尿、尿频和排尿疼痛持续约一年半入院。膀胱镜检查发现膀胱后壁和左侧壁有4个实体瘤,伴有弥漫性黏膜充血。肿瘤活检显示为腺癌。临床检查发现该病例无膀胱外原发性恶性肿瘤。1981年1月22日进行了根治性膀胱切除术并采用回肠导管进行尿流改道。组织学检查显示肿瘤是起源于膀胱黏膜的腺癌。自手术以来三年多的随访未显示任何肿瘤复发迹象或膀胱外恶性肿瘤的发生。此外,对日本过去25年报告的28例原发性膀胱腺癌病例进行了回顾和分析。