Obari Abdulkader, Sano Toshiaki, Ohyama Kenichi, Kudo Eiji, Qian Zhi Rong, Yoneda Akiko, Rayhan Nasim, Mustafizur Rahman Muhammad, Yamada Shozo
Department of Human Pathology, Institute of Health Bioscience, The University of Tokushima Graduate School, 3-18-15 Kuramoto, Tokushima, Japan.
Endocr Pathol. 2008 Summer;19(2):82-91. doi: 10.1007/s12022-008-9029-z.
Pituitary adenomas producing almost exclusively growth hormones (GH) have been ultrastructurally classified into two distinct types: densely granulated somatotroph (DG) adenomas and sparsely granulated (SG) adenomas. Fibrous body (FB), an intracytoplasmic globular aggregation of cytokeratin (CK) filaments, is a hallmark of SG adenomas. Under light microscope, FB could be identified by CK immunohistochemistry as a dot-pattern immunoreaction versus a perinuclear pattern for cells without FB. However, it has been noted that numerous adenomas contain mixed populations of the two patterns. To clarify clinicopathological characteristics of the adenomas with mixed populations ("intermediate type" adenomas) and to confirm clinicopathological differences between strictly defined DG-type and SG-type adenomas, we performed this study on 104 GH cell adenomas. Having segregated "intermediate-type" adenomas (26 cases), we found significant differences between typical DG-type (47 cases) and SG-type adenomas (31 cases); SG-type adenomas had younger ages (44 vs. 50), higher frequency of macroadenomas (86% vs. 58%), invasiveness (65% vs. 38%), advanced grades (3 or 4) in Knosp's classification (50% vs. 24%), and weaker immunoreaction for GH, beta-TSH, alpha-subunit, E-cadherin, and beta-catenin. Clinicopathological characteristics of "intermediate-type" adenomas were identical to those of DG-type adenomas. These findings confirm that SG-type adenoma is a distinct section of GH cell adenomas with special properties and biological behavior, and suggest that intermediate-phenotype adenomas are enrolled in DG-type adenomas. Special properties and biological behavior of SG-type adenomas may appear after the majority of tumor cells possess a fully developed fibrous body.
几乎仅分泌生长激素(GH)的垂体腺瘤在超微结构上可分为两种不同类型:密集颗粒型生长激素细胞(DG)腺瘤和稀疏颗粒型(SG)腺瘤。纤维小体(FB)是细胞角蛋白(CK)丝在胞质内形成的球状聚集物,是SG腺瘤的一个标志。在光学显微镜下,通过CK免疫组织化学可将FB识别为点状免疫反应,而无FB的细胞则呈现核周型免疫反应。然而,已经注意到许多腺瘤包含这两种模式的混合细胞群。为了阐明具有混合细胞群的腺瘤(“中间型”腺瘤)的临床病理特征,并确认严格定义的DG型和SG型腺瘤之间的临床病理差异,我们对104例GH细胞腺瘤进行了这项研究。在分离出“中间型”腺瘤(26例)后,我们发现典型的DG型(47例)和SG型腺瘤(31例)之间存在显著差异;SG型腺瘤患者年龄较轻(44岁对50岁),大腺瘤发生率较高(86%对58%),侵袭性较高(65%对38%),在克诺斯普分类中高级别(3或4级)的比例较高(50%对24%),并且对GH、β-促甲状腺激素、α亚基、E-钙黏蛋白和β-连环蛋白的免疫反应较弱。“中间型”腺瘤的临床病理特征与DG型腺瘤相同。这些发现证实SG型腺瘤是具有特殊性质和生物学行为的GH细胞腺瘤的一个独特亚型,并表明中间表型腺瘤应归入DG型腺瘤。SG型腺瘤的特殊性质和生物学行为可能在大多数肿瘤细胞拥有完全发育的纤维小体后出现。