畸胎瘤、瘤变和分化:生物学综述。1 .畸胎瘤的自然史。

Investigative & cell pathology Pub Date : 1978-01-01
M J O'Hare
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引用次数: 0

摘要

在本文中,我试图概述自发发生的畸胎瘤和相关肿瘤的自然历史,但没有引入任何关于其组织发生或内部分化机制的先入之见或假设。这种遗漏的理由是,除了LINDER等人最近的研究(1975a, b)外,目前还没有直接证据表明这两种过程在人类肿瘤中都存在。畸胎瘤样病变的各种组织病理学分类也没有详细讨论,因为它们在很大程度上是根据经验基础或某些组织遗传学假设进化而来的,以服务于特定的预后目的。在任何一种情况下,都有一种不可避免的趋势,即以牺牲结构和行为的可能连续性为代价,强调形态外观的极端。相反,本文的目的是辨别这些肿瘤的共同特征,无论何时何地发生。因此,人类畸胎瘤是一种独特的纯组织病变,至少潜在地由几乎每一种可识别的(可能还有一些尚未识别的)胚胎、胎儿和成人细胞和组织类型组成,在某些情况下,还包括没有明显来源或分化的恶性细胞。尽管偶尔出现类似体前胚胎(胚状体)的结构,但没有令人信服的证据表明人类畸胎瘤组织发生以任何严格的方式重述胚胎发生。组织学上,压倒性的印象是细胞和组织在不同的发育和分化阶段或多或少的随机关联,直到但不超过器官发生。这种畸胎瘤在许多明确的部位发现,其中婴儿期的骶尾骨最突出,成年期的性腺最突出。性腺和性腺外部位也与明显同质的肿瘤有关,肿瘤细胞具有生发分化早期的特征,在许多情况下,会引起明显的基质和淋巴细胞反应,即所谓的生发瘤。在越来越多的病例中发现的“混合性”肿瘤中,至少在一些肿瘤中,有核学证据表明畸胎瘤和生发瘤的成分是联合的,而不是分开的,这挑战了长期以来认为它们总是分开的观点(例如HALLEY, 1963)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Teratomas, neoplasia and differentiation: a biological overview. I. The natural history of teratomas.

In this paper I have attempted to outline the natural history of spontaneously occurring teratomas and associated tumours, but without introducing any preconceptions or assumptions as to their histogenesis or mechanisms of internal differentiation. The justification for this omission is that there is presently no direct evidence in respect of either process in human tumours of this type, with the exception of recent work by LINDER et al. (1975a, b). The various histopathological classifications of teratoid lesions have not been discussed in detail either, because for the most part they have been evolved to serve a specific prognostic purpose on either an empirical basis or on certain histogenetic assumptions. In either case there is an inevitable tendency to emphasize extremes of morphological appearance at the expense of possible continuities of structure and behaviour across the spectrum of teratoid lesions. The purpose of this paper, on the contrary, has been to discern features common to these tumours whenever and wherever they occur. Thus, human teratomas are uniquely puritissular lesions composed, potentially at least, of virtually every recognizable (and probably some as yet unrecognizable), type of embryonic, foetal and adult cell and tissue, together with, in some cases, frankly malignant cells of no obvious derivation or differentiation. In spite of the occasional appearance of structures resembling pre-somite embryos (embryoid bodies), there is no compelling evidence that human teratomatous histogenesis recapitulates embryogenesis in any strict fashion. Histologically, the overwhelming impression is of a more or less random association of cells and tissues at different stages of development and differentiation that proceed up to but not beyond organogenesis. Such teratomas are found at a number of well-defined sites, of which the sacrococcyx is the most prominent in infancy and the gonads during adult life. Both gonadal and extragonadal sites are also associated with apparently homogeneous neoplasms containing cells with features reminiscent of early stages of germinal differentiation which evoke, in many cases, a marked stromal and lymphocytic response, the so-called germinomas. In 'mixed' tumours, which are recognized in an increasing proportion of cases, there is karyological evidence of a conjoint rather than separate origin of teratomatous and germinomatous elements in at least some tumours, challenging a long held belief in their invariably separate character (e.g. HALLEY, 1963).

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