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[泌尿道非尿路上皮肿瘤]

[Non-urothelial tumors of the urinary tract].

作者信息

Mikuz G

机构信息

Pathologisches Institut der Universität Innsbruck.

出版信息

Verh Dtsch Ges Pathol. 1993;77:180-98.

PMID:7511278
Abstract

Only about 2% of the urinary tract are not of urothelial origin. Our knowledge of their morphology and biology is mainly based on single case reports, and therefore apart from a few exceptions very poor. Generally, the most often affected site is the urinary bladder (79.2%), followed by the urethra (12.7%), pelvis (4.9%) and ureter (3.2%). The urinary bladder also is the only organ in which all different histological types of these tumors were described. According to their histogenesis non-urothelial tumors (NUT) can be classified by the following main groups: soft tissue tumors, mixed epithelial and non epithelial tumors (carcinosarcomas), neuroendocrine carcinomas, carcinoids, malignant lymphomas, malignant melanomas and extragonadal germ cell tumors. Moreover some very interesting tumor-like lesions, like malakoplakia and inflammatory pseudosarcoma, mainly occur in this region. About 75% of all NUT of the urinary tract belong to the soft tissue tumors. Rhabdomyosarcomas in children and leiomyomas and -myosarcomas in adults are the more frequent histological types. Leiomyosarcomas can easily be confused with other tumor types or even with inflammatory pseudotumors. The use of immunohistochemistry to achieve a correct diagnosis is mandatory but not always successful. A relatively frequent tumor occurring in the bladder of young adults is the paraganglioma (pheochromocytoma), which usually produces typical symptoms of catecholamine excess. Carcinosarcomas of the urinary bladder contain both epithelial and mesenchymal components. They have to be distinguished from collision tumors (coexistent but separate carcinoma and sarcoma), spindle cell transitional carcinomas as well as from carcinomas with osseous or cartilaginous metaplasia. Carcinoids and neuroendocrine carcinomas developed from the neuroendocrine cells scattered all over the transitional epithelium of the bladder. Neuroendocrine carcinomas of the bladder are also called "oat cell carcinomas" since they show the same histological features and immunoreactivity as the oat cell carcinomas of the lung. They share also the same poor prognosis. The affection of the urinary tract in generalized malignant lymphomas and leukemias occur in more than 30% of cases. Lymphomas, primarily localised in the urinary bladder are, however, extremely rare. The most frequent ones are low grade non Hodgkin lymphomas, although 3 cases of Hodgkin disease and a few cases of primary extramedullary plasmacytoma of the bladder have been reported, too.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

只有约2%的泌尿道并非尿路上皮起源。我们对其形态学和生物学的了解主要基于个别病例报告,因此,除了少数例外情况,了解非常有限。一般来说,最常受累的部位是膀胱(79.2%),其次是尿道(12.7%)、肾盂(4.9%)和输尿管(3.2%)。膀胱也是唯一一个描述了所有不同组织学类型这类肿瘤的器官。根据其组织发生,非尿路上皮肿瘤(NUT)可分为以下主要类别:软组织肿瘤、上皮和非上皮混合性肿瘤(癌肉瘤)、神经内分泌癌、类癌、恶性淋巴瘤、恶性黑色素瘤和性腺外生殖细胞肿瘤。此外,一些非常有趣的肿瘤样病变,如软斑病和炎性假肉瘤,主要发生在该区域。泌尿道所有NUT中约75%属于软组织肿瘤。儿童横纹肌肉瘤以及成人平滑肌瘤和平滑肌肉瘤是较常见的组织学类型。平滑肌肉瘤很容易与其他肿瘤类型甚至炎性假瘤混淆。使用免疫组织化学来做出正确诊断是必要的,但并不总是成功。发生在年轻成人膀胱的一种相对常见的肿瘤是副神经节瘤(嗜铬细胞瘤),通常会产生典型的儿茶酚胺过量症状。膀胱癌肉瘤包含上皮和间充质成分。它们必须与碰撞瘤(并存但独立的癌和肉瘤)、梭形细胞移行癌以及伴有骨或软骨化生的癌相区分。类癌和神经内分泌癌由散布在膀胱移行上皮各处的神经内分泌细胞发展而来。膀胱神经内分泌癌也被称为“燕麦细胞癌”,因为它们与肺燕麦细胞癌具有相同的组织学特征和免疫反应性。它们的预后也同样很差。全身性恶性淋巴瘤和白血病累及泌尿道的情况在超过30%的病例中出现。然而,主要局限于膀胱的淋巴瘤极其罕见。最常见的是低级别非霍奇金淋巴瘤,不过也有3例霍奇金病以及少数膀胱原发性髓外浆细胞瘤的病例报告。(摘要截断于400字)

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