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小儿膀胱恶性肿瘤的最新进展

Recent advances in pediatric bladder malignancies.

作者信息

Lopes Roberto Iglesias, Mello Marcos Figueiredo, Lorenzo Armando J

机构信息

Pediatric Urology Unit, Division of Urology, Hospital das Clínicas, University of São Paulo Medical School, São Paulo, 05402-000, Brazil.

Division of Urology, The Hospital for Sick Children and Department of Surgery, University of Toronto, Toronto, ON, Canada.

出版信息

F1000Res. 2020 Feb 25;9. doi: 10.12688/f1000research.19396.1. eCollection 2020.

Abstract

Urothelial pediatric neoplasms are relatively rare. Papillary urothelial neoplasms of low malignant potential (PUNLMPs) and rhabdomyosarcoma (RMS) are the most common bladder malignancies in the pediatric population. Clinical presentation encompasses macroscopic hematuria or lower urinary tract symptoms (or both) or is detected incidentally at imaging. Tumors arising from the bladder can originate from any of its four histological layers (urothelium, lamina propria, detrusor, and adventitia) and are divided into tumors that have an epithelial origin (arising from the urothelium) and those that have a non-epithelial origin (mesenchymal neoplasms). RMS is the most common malignant tumor of the urinary bladder in children younger than 10 years. Deriving from the embryonic mesenchymal cell, the histopathologic subtypes of RMS are embryonal RMS (>90%) and alveolar histology (<10%). Pre-treatment imaging should be carried out by computed tomography (CT) or at present is more likely with magnetic resonance imaging of the pelvis. Chest CT and bone scintigraphy are used to screen for metastases. In selected cases, a positron emission tomography scan may be recommended to evaluate suspicious lesions. The current prognostic classification considers age, histologic subtype, tumor site, size, and extent (nodal or distant metastases). Staging is based on pre-operative findings, group is based on intra-operative findings and pathology, and risk stratification is derived from both stage and group data. Pre-operative chemotherapy is the most common first-line intervention for bladder/prostate RMS, before surgery or radiation therapy. Collaborative groups such as the Soft Tissue Sarcoma Committee of the Children's Oncology Group and the European Pediatric Soft Tissue Sarcoma Study Group endorse this therapy. PUNLMPs are generally solitary, small (1-2 cm), non-invasive lesions that do not metastasize. Therapy is usually limited to a transurethral resection of the bladder tumor. About 35% are recurrent and around 10% of them increase in size if they are not treated.

摘要

小儿尿路上皮肿瘤相对罕见。低恶性潜能乳头状尿路上皮肿瘤(PUNLMPs)和横纹肌肉瘤(RMS)是小儿人群中最常见的膀胱恶性肿瘤。临床表现包括肉眼血尿或下尿路症状(或两者兼有),或在影像学检查时偶然发现。膀胱肿瘤可起源于其四层组织学结构(尿路上皮、固有层、逼尿肌和外膜)中的任何一层,分为上皮起源肿瘤(起源于尿路上皮)和非上皮起源肿瘤(间叶性肿瘤)。RMS是10岁以下儿童最常见的膀胱恶性肿瘤。RMS起源于胚胎间充质细胞,其组织病理学亚型为胚胎型RMS(>90%)和肺泡型组织学(<10%)。治疗前成像应通过计算机断层扫描(CT)进行,目前更可能采用盆腔磁共振成像。胸部CT和骨闪烁显像用于筛查转移情况。在某些情况下,可能建议进行正电子发射断层扫描以评估可疑病变。目前的预后分类考虑年龄、组织学亚型、肿瘤部位、大小和范围(淋巴结或远处转移)。分期基于术前检查结果,分组基于术中检查结果和病理,风险分层则来自分期和分组数据。术前化疗是膀胱/前列腺RMS最常见的一线干预措施,在手术或放疗之前进行。儿童肿瘤学组软组织肉瘤委员会和欧洲小儿软组织肉瘤研究组等协作组织支持这种治疗方法。PUNLMPs通常为孤立性、小(1 - 2厘米)、非侵袭性病变,不会发生转移。治疗通常限于经尿道膀胱肿瘤切除术。约35%会复发,如果不治疗,其中约10%会增大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a6/7043112/88a7358d0447/f1000research-9-21262-g0000.jpg

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