Asa S L, Kovacs K
Department of Pathology, St. Michael's Hospital, University of Toronto, Ontario, Canada.
Can J Neurol Sci. 1992 May;19(2):228-35.
Clinically non-functioning pituitary adenomas are morphologically classified into two groups, those which have hormone immunoreactivity and ultrastructural features of known adenohypophysial cell types but are clinically silent, and those composed of cells that do not resemble nontumorous adenohypophysial cell types. Among the former are the silent somatotroph adenomas, silent corticotroph adenomas and silent gonadotroph adenomas; the latter include the silent type III adenomas, null cell adenomas and oncocytomas. We review their histological, immunohistochemical and ultrastructural features, the results of in situ hybridization to determine hormone synthesis by these tumors and data obtained from tissue culture characterizing their hormone release in vitro. Non-functioning adenomas represent a heterogeneous group. The discrepancies between morphology, immunoreactivity and lack of endocrine activity of silent adenomas are not clear. Oncocytomas are variants of null cell adenomas. We suggest that null cell adenomas and oncocytomas originate in uncommitted pluripotent precursor cells capable of undergoing multidirectional differentiation. The progenitor cells differentiate most frequently toward FSH/alpha-subunit producing cells; the mechanism of preferential differentiation is obscure.
临床无功能垂体腺瘤在形态学上分为两组,一组具有已知腺垂体细胞类型的激素免疫反应性和超微结构特征,但临床上无明显症状,另一组由与非肿瘤性腺垂体细胞类型不同的细胞组成。前者包括静止性生长激素细胞腺瘤、静止性促肾上腺皮质激素细胞腺瘤和静止性促性腺激素细胞腺瘤;后者包括静止性III型腺瘤、无功能细胞腺瘤和嗜酸细胞瘤。我们回顾了它们的组织学、免疫组织化学和超微结构特征、通过原位杂交确定这些肿瘤激素合成的结果以及从组织培养获得的表征其体外激素释放的数据。无功能腺瘤是一个异质性群体。静止性腺瘤的形态、免疫反应性和内分泌活性缺乏之间的差异尚不清楚。嗜酸细胞瘤是无功能细胞腺瘤的变体。我们认为无功能细胞腺瘤和嗜酸细胞瘤起源于能够进行多向分化的未定向多能前体细胞。祖细胞最常分化为产生促卵泡激素/α亚基的细胞;优先分化的机制尚不清楚。