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原发性淀粉样变性局限于膀胱

[Primary amyloidosis localized in the bladder].

作者信息

Vicioso Recio L, Macías Jiménez N, Castro Leon A, Gutiérrez Bueso M, García González I

机构信息

Servicio de Urología, Hospital General Básico de Antequera, Málaga, España.

出版信息

Arch Esp Urol. 1995 Nov;48(9):963-6.

PMID:8554407
Abstract

OBJECTIVE

We report a case of localized amyloidosis of the urinary bladder in an 80-year-old female whose main presenting symptom was massive hematuria.

METHODS

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.

RESULTS

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.

CONCLUSIONS

Primary localized amyloidosis of the urinary bladder is a rare condition that can be successfully treated surgically and has an excellent prognosis.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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