Takahashi H, Fujita S, Tsuda N, Tezuka F, Okabe H
Department of Oral Pathology, Nagasaki University School of Dentistry.
Tohoku J Exp Med. 1990 Sep;162(1):79-93. doi: 10.1620/tjem.162.79.
Twenty-five benign pleomorphic adenomas of salivary glands in children were studied with immunohistochemical techniques in order to characterize the cell types comprising the epithelial and so-called "mesenchymal" regions of the tumors. The antisera against alpha 1-antichymotrypsin (alpha 1-ACT) and alpha 1-antitrypsin (alpha 1-AT) were used to stain in normal salivary gland tissue as well as in pleomorphic adenoma. In normal salivary glands, alpha 1-ACT was localized to the intercalated duct and serous acinar cells. On the other hand, there was positive staining for alpha 1-AT in the intercalated and striated duct cells. Twenty-five cases (100%) of pleomorphic adenomas in children displayed positivity to alpha 1-ACT staining and 22 cases (88%) showed a positive staining for alpha 1-AT. alpha 1-ACT staining was particularly intense in chondrocyte-like cells of 20 cases (80%), in inner tubular cells of 16 (64%) and cyst-lining cells of 12 (52%). The limited number of tumor cells which were called plasmatoid or hyaline cells and squamous epithelial cells, were positive for alpha 1-ACT. None of the outer tubular cells and hyalinous material was positively stained for alpha 1-ACT. A strong positive reaction for alpha 1-AT was observed in chondrocyte-like cells of 15 cases (60%). Inner tubular cells were positive for alpha 1-AT in 12 cases (48%), plasmatoid or hyaline cells in 10 (40%) and cyst-lining cells in 8 (35%). Squamous epithelial cells, clear cells, secretory product and hyalinous material were positive for alpha 1-AT in some cases. Chondroid matrix and myxoid stroma had no reaction with both antibodies. The biological role of alpha 1-ACT and alpha 1-AT with a wide immunohistochemical distribution in pleomorphic adenomas of children may be associated with a self regulating mechanism which inhibits degradation by tissue proteinases.
采用免疫组织化学技术对25例儿童涎腺良性多形性腺瘤进行研究,以明确构成肿瘤上皮及所谓“间充质”区域的细胞类型。抗α1 -抗糜蛋白酶(α1 - ACT)和α1 -抗胰蛋白酶(α1 - AT)的抗血清用于正常涎腺组织及多形性腺瘤的染色。在正常涎腺中,α1 - ACT定位于闰管和浆液性腺泡细胞。另一方面,闰管和纹状管细胞对α1 - AT呈阳性染色。25例(100%)儿童多形性腺瘤对α1 - ACT染色呈阳性,22例(88%)对α1 - AT染色呈阳性。α1 - ACT染色在20例(80%)的软骨样细胞、16例(64%)的内管状细胞和12例(52%)的囊肿衬里细胞中尤为强烈。少数被称为浆细胞样或透明细胞以及鳞状上皮细胞的肿瘤细胞对α1 - ACT呈阳性。所有外管状细胞和透明物质对α1 - ACT均无阳性染色。15例(60%)的软骨样细胞对α1 - AT呈强阳性反应。12例(48%)的内管状细胞、10例(40%)的浆细胞样或透明细胞和8例(35%)的囊肿衬里细胞对α1 - AT呈阳性。鳞状上皮细胞、透明细胞、分泌产物和透明物质在某些情况下对α1 - AT呈阳性。软骨样基质和黏液样间质对两种抗体均无反应。α1 - ACT和α1 - AT在儿童多形性腺瘤中广泛的免疫组织化学分布的生物学作用可能与抑制组织蛋白酶降解的自我调节机制有关。