Vicioso Recio L, Macías Jiménez N, Castro Leon A, Gutiérrez Bueso M, García González I
Servicio de Urología, Hospital General Básico de Antequera, Málaga, España.
Arch Esp Urol. 1995 Nov;48(9):963-6.
We report a case of localized amyloidosis of the urinary bladder in an 80-year-old female whose main presenting symptom was massive hematuria.
Cystoscopic examination revealed a tumor on the trigone and bladder neck. A transurethral resection of the tumor was performed and the fragments were processed for histopathological study with hematoxylin-eosin and Congo red staining and ultrastructural study.
The histopathological analyses disclosed large eosinophilic deposits in the submucosa with birefringence under polarized light in Congo red staining. Electron microscopy revealed a meshwork of filaments typical of amyloid. The patient had no symptoms or signs of systemic disease and remains symptom-free four years later.
Primary localized amyloidosis of the urinary bladder is a rare condition that can be successfully treated surgically and has an excellent prognosis.
我们报告一例80岁女性膀胱局限性淀粉样变性病例,其主要表现症状为大量血尿。
膀胱镜检查发现三角区和膀胱颈部有一肿瘤。行经尿道肿瘤切除术,将切除组织碎片进行苏木精-伊红染色和刚果红染色的组织病理学研究以及超微结构研究。
组织病理学分析显示黏膜下层有大量嗜酸性沉积物,刚果红染色在偏振光下呈双折射。电子显微镜显示典型的淀粉样细丝网状结构。该患者无全身疾病的症状或体征,四年后仍无症状。
膀胱原发性局限性淀粉样变性是一种罕见疾病,可通过手术成功治疗,预后良好。