Vidal S, Syro L, Horvath E, Uribe H, Kovacs K
Department of Laboratory Medicine and Pathobiology, St. Michael's Hospital, University of Toronto, Canada.
Ultrastruct Pathol. 1999 May-Jun;23(3):141-8. doi: 10.1080/019131299281635.
Monomorphous pituitary adenomas expressing several hormones by immunocytochemistry are common, whereas adenomas displaying multiple immunoreactivities and consisting of more than one morphologic cell types are rare. Three such unusual pituitary adenomas, surgically removed from two patients with acromegaly and one patient with hyperprolactinemia, were investigated by histology, immunocytochemistry, transmission electron microscopy, as well as immunoelectron microscopy using double immunogold labeling. Immunocytochemistry revealed variable degrees of immunoreactivities for growth hormone (GH), prolactin (PRL), thyroid-stimulating hormone (beta-TSH), and alpha-subunit of glycoprotein hormones in all three tumors. The three adenomas consisted of phenotypically diverse cell populations as documented by transmission electron microscopy. In addition to monohormonal GH cells, immunoelectron microscopy demonstrated numerous cells colocalizing GH and PRL or GH and beta-TSH, and rarely PRL and beta-TSH in tumors of acromegalics. The adenoma causing hyperprolactinemia consisted chiefly of mammosomatotrophs colocalizing PRL and GH, whereas beta-TSH labeling was scant. The three tumors in the study were selected from a cluster of five plurimorphous plurihormonal adenomas received from the same locale where they accounted for an unprecedented 21% of adenomas producing GH and/or PRL. The enhanced susceptibility to develop plurimorphous adenomas of the acidophil cell line may have a genetic basis in the stable population the patients came from.
免疫细胞化学显示表达多种激素的单形性垂体腺瘤很常见,而显示多种免疫反应性且由不止一种形态学细胞类型组成的腺瘤则很罕见。对从两名肢端肥大症患者和一名高催乳素血症患者身上手术切除的三例这种不寻常的垂体腺瘤进行了组织学、免疫细胞化学、透射电子显微镜以及使用双免疫金标记的免疫电子显微镜研究。免疫细胞化学显示,在所有三例肿瘤中,生长激素(GH)、催乳素(PRL)、促甲状腺激素(β-TSH)和糖蛋白激素α亚基均有不同程度的免疫反应性。透射电子显微镜记录显示,这三例腺瘤由表型多样的细胞群体组成。除了单激素性GH细胞外,免疫电子显微镜还显示,在肢端肥大症患者的肿瘤中,有许多细胞同时存在GH和PRL或GH和β-TSH,很少有PRL和β-TSH同时存在。导致高催乳素血症的腺瘤主要由同时存在PRL和GH的乳腺生长激素细胞组成,而β-TSH标记很少。本研究中的三例肿瘤是从同一地区接收的一组五例多形性多激素腺瘤中挑选出来的,在该地区,它们占产生GH和/或PRL腺瘤的21%,这一比例前所未见。嗜酸细胞系多形性腺瘤发生易感性增强可能在患者来自的稳定人群中有遗传基础。