Kunze E
Center of Pathology of the University of Göttingen, Germany.
Exp Toxicol Pathol. 1998 Sep;50(4-6):341-55. doi: 10.1016/S0940-2993(98)80015-8.
The histogenesis of nonurothelial carcinomas (squamous cell carcinoma, common adenocarcinoma, clear cell adenocarcinoma, signet ring cell adenocarcinoma and undifferentiated carcinomas) of the urinary bladder is difficult to understand, since the bladder is normally lined exclusively by transitional cell epithelium and contains no otherwise specified epithelia. In the present study we analysed the morphology and development of nontransitional cell carcinomas of the human and comparatively of the rat urinary bladder in an attempt to elucidate their histogenetic derivation. There is strong evidence that the underlying histogenetic principle consists in the well-known pluripotent metaplastic potency (squamous, columnar, goblet and signet ring cell, glandular and so-called nephrogenic metaplasia) of the normal and neoplastic urothelium as well, due to the complex embryologic origin of the bladder. Our findings indicate that squamous cell carcinomas, common and clear cell adenocarcinomas, and signet ring cell adenocarcinomas mainly arise secondarily from preexisting, predominantly solid transitional cell carcinomas by focally beginning and diffusely progressing metaplastic changes of various types. The second histogenetic pathway consists in the formation from primary metaplasias of the transitional cell epithelium in situ. Undifferentiated carcinomas (small, large and sarcomatoid subtypes) develop from preexistent solid urothelial carcinomas by a cellular dedifferentiation. Recognition of transitional cell carcinomas characterised by focal metaplastic processes or cellular dedifferentiation seems to be important from a clinical point of view, because of their probably more malignant biologic behaviour compared with uniformly differentiated pure urothelial carcinomas. Our comparative morphologic analysis of nonurothelial carcinomas and their histogenesis has demonstrated that the findings in the human and rat urinary bladder are largely identical. The experimental models used permit reliable extrapolation of the results obtained to the situation in man.
膀胱非尿路上皮癌(鳞状细胞癌、普通腺癌、透明细胞腺癌、印戒细胞腺癌和未分化癌)的组织发生难以理解,因为膀胱正常情况下仅由移行细胞上皮衬里,不含其他特定上皮。在本研究中,我们分析了人类及相对地大鼠膀胱非移行细胞癌的形态和发展,试图阐明其组织发生来源。有强有力的证据表明,由于膀胱复杂的胚胎起源,潜在的组织发生原理在于正常和肿瘤性尿路上皮众所周知的多能化生潜能(鳞状、柱状、杯状和印戒细胞、腺性以及所谓的肾源性化生)。我们的研究结果表明,鳞状细胞癌、普通和透明细胞腺癌以及印戒细胞腺癌主要继发于先前存在的、主要为实性的移行细胞癌,通过局部开始并弥漫性进展的各种类型化生改变形成。第二条组织发生途径在于原位移行细胞上皮原发性化生的形成。未分化癌(小、大及肉瘤样亚型)由先前存在的实性尿路上皮癌通过细胞去分化发展而来。从临床角度来看,识别以局灶性化生过程或细胞去分化为特征的移行细胞癌似乎很重要,因为与均匀分化的纯尿路上皮癌相比,它们可能具有更恶性的生物学行为。我们对非尿路上皮癌及其组织发生的比较形态学分析表明,人类和大鼠膀胱的研究结果基本相同。所使用的实验模型允许将获得的结果可靠地外推至人类情况。