Department of Urology, Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Department of Internal Medicine, Chengdu Shuangliu Hospital of Traditional Chinese Medicine, Chengdu, Sichuan, China.
BMC Urol. 2021 Jul 8;21(1):98. doi: 10.1186/s12894-021-00863-y.
Nonfunctional bladder paragangliomas is a rare urological disease. It may present clinical, radiology and pathological features similar to bladder cancer, Only scarce reports have been reported. Urologist must identify this generally benign neuroendocrine neoplasm to avoid misdiagnosis.
A 62-year-old female presented the outpatient department of our hospital with the symptoms of stomachache, frequent micturition, and urination pain for 20 days. Diagnosed with high blood pressure 1 year ago, administered Amlodipine besylate tablets 5 mg po qd occasionally, did not check blood pressure; denied any tumor observation in the family history. Color ultrasound of the urinary system showed a 38 mm × 34 mm hypoechoic mass on the right side of the bladder, CDFI: in the masses, blood supply was sufficient. Cystoscope showed bladder occupying lesion. Biopsy diagnosis: papillary polypoid cystitis was suspected as a malignant change (Fig. 3a). Then, the patient was admitted to our urological department. Further, computer tomography urography considered bladder cancer. Cystoscopy and biopsy failed to define the nature of the lesions in our outpatient department, which prompted a transurethral resection of the bladder tumor. histopathological and immunohistochemical results were diagnosed as bladder paragangliomas. For the reason, the tumor was removed by partial resection of the bladder. The postoperative recovery and follow-up were uneventful.
Nonfunctional bladder paragangliomas are occasionally found on imaging studies with the symptoms of urinary tract infection or/and intermittent painless hematuria. It may present clinical, radiology and pathological features similar to bladder cancer, so knowledge of this generally benign neuroendocrine neoplasm is of great importance to avoid misdiagnosis. It should be accompanied by the clinical and pathological characteristics of the patient and image changes. Partial resection of the bladder can effectively treat this disease.
无功能膀胱副神经节瘤是一种罕见的泌尿科疾病。它可能表现出与膀胱癌相似的临床、影像学和病理学特征,仅有少量报道。泌尿科医生必须识别出这种通常为良性的神经内分泌肿瘤,以避免误诊。
一名 62 岁女性因腹痛、尿频和尿痛 20 天到我院门诊就诊。1 年前诊断为高血压,偶尔口服氨氯地平 5mg,未监测血压;否认家族中有任何肿瘤观察史。泌尿系统彩色超声显示右侧膀胱有一个 38mm×34mm 的低回声肿块,CDFI:肿块内血供丰富。膀胱镜检查显示膀胱占位性病变。活检诊断:疑为恶性改变的乳头状息肉状膀胱炎(图 3a)。随后,患者被收入我泌尿科病房。进一步的计算机断层尿路造影考虑为膀胱癌。膀胱镜检查和活检未能明确门诊病变的性质,提示行经尿道膀胱肿瘤电切术。组织病理学和免疫组织化学结果诊断为膀胱副神经节瘤。由于该肿瘤,行部分膀胱切除术切除肿瘤。术后恢复和随访均无异常。
无功能膀胱副神经节瘤偶尔在影像学检查中发现,伴有尿路感染或/和间歇性无痛性血尿的症状。它可能表现出与膀胱癌相似的临床、影像学和病理学特征,因此了解这种通常为良性的神经内分泌肿瘤非常重要,以避免误诊。它应伴有患者的临床和病理特征以及图像变化。部分膀胱切除术可有效治疗该病。