Ewing's sarcoma of the urinary bladder - the urologic and pathologic differential diagnosis and current therapeutic options.

Q4 Medicine Klinicka Onkologie Pub Date : 2023-01-01
M Král, D Kurfúrstová, I Hartmann, H Študentová, J Škarda
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引用次数: 0

Abstract

Background: Bladder cancer is 11th most common cancer worldwide. Histologically, most of the tumors are classified as urothelial carcinomas. Less common variants (squamous cell or adenocarcinomas) usually comprise up to 10% of cases. Other types of tumors are exceptional. The finding of Ewing's sarcoma in the bladder is considered extremely rare.

Case: We present the case of a 54-year-old female patient examined for painless hematuria. During the follow-up examination, a bulky tumor of the bladder was detected, but considering the extent of the bladder tumor, only a diagnostic transurethral resection was possible. According to the primary staging, the disease was already advanced at the time of admission with metastatic spread, anemia and present obstruction of the upper urinary tract.

Results: Histologically, Ewing's sarcoma was surprisingly demonstrated in the urinary bladder. Anemia caused by hematuria and advanced disease was corrected by blood transfusions and obstruction of the right kidney by puncture nephrostomy. However, despite a very quick diagnosis, completion of staging and preparation of the patient for further treatment, the patient had died before the planned systemic treatment began.

Conclusion: The diagnosis of Ewing's sarcoma is identical to that of the other bladder tumors, i.e. transurethral resection. In the case of confirmation of this histological type, it is necessary to complete staging examinations and start multimodal treatment. Early systemic chemotherapy plays a key role and if metastatic spread is excluded, radical cystectomy or radiotherapy are included, too. The aim of our communication is to present a rare case of this disease, discuss the differential diagnosis and point out the principles and possibilities of its treatment.

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膀胱尤文氏肉瘤--泌尿学和病理学鉴别诊断及当前治疗方案。
背景:膀胱癌是全球第 11 位最常见的癌症:膀胱癌是全球第 11 位最常见的癌症。在组织学上,大多数肿瘤被归类为尿路上皮癌。较少见的变种(鳞状细胞癌或腺癌)通常占病例的 10%。其他类型的肿瘤则比较少见。在膀胱中发现尤文氏肉瘤的病例极为罕见:本病例是一名 54 岁的女性患者,因无痛性血尿接受检查。在随访检查中,发现膀胱内有一个巨大肿瘤,但考虑到膀胱肿瘤的范围,只能进行诊断性经尿道切除。根据初诊分期,患者入院时病情已属晚期,出现转移扩散、贫血和上尿路梗阻:组织学检查显示,膀胱中竟然有尤文氏肉瘤。血尿和晚期疾病导致的贫血通过输血得到了纠正,右肾梗阻通过穿刺肾造瘘术得到了治疗。然而,尽管诊断、分期和进一步治疗的准备工作很快就完成了,但患者还是在计划的系统治疗开始之前去世了:结论:尤文肉瘤的诊断与其他膀胱肿瘤的诊断相同,即经尿道切除。如果确诊为这种组织学类型,就必须完成分期检查并开始多模式治疗。早期全身化疗起着关键作用,如果排除了转移扩散的可能性,还可以进行根治性膀胱切除术或放疗。我们的文章旨在介绍这种疾病的一个罕见病例,讨论鉴别诊断,并指出治疗原则和可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Klinicka Onkologie
Klinicka Onkologie Medicine-Oncology
CiteScore
1.00
自引率
0.00%
发文量
37
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