Characterization of the cellular component of polymorphous low-grade adenocarcinoma by immunohistochemistry and electron microscopy

被引:37
作者
Araújo, V
Sousa, S
Jaeger, M
Jaeger, R
Loyola, A
Crivelini, M
Araújo, N
机构
[1] Univ Sao Paulo, Sch Dent, Fac Odontol, BR-05508900 Sao Paulo, Brazil
[2] Univ Fed Uberlandia, Sch Dent, Uberlandia, MG, Brazil
[3] Paulista State Univ, Sch Dent, Aracatuba, Brazil
来源
ORAL ONCOLOGY | 1999年 / 35卷 / 02期
关键词
salivary gland tumors; polymorphous low-grade adenocarcinoma; intermediate filaments; actin; immunohistochemistry; transmission electron microscopy;
D O I
10.1016/S1368-8375(98)00102-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In order to characterize the cellular component of the polymorphous low-grade adenocarcinoma (PLGA) of the salivary gland, a morphological and immunohistochemical study was carried out. Thirty cases of PLGA were studied by light microscopy and immunohistochemistry and five cases by transmission electron microscopy (TEM). The expression of cytokeratins (CKs) 7,8,10,13,14,18,19, vimentin and muscle-specific actin (MSA) was investigated through the streptavidin-biotin method. The majority of tumor cells stained for vimentin, CKs 8,18 and 7. CK 14 was positive in most cells of the papillary and trabecular sub-types. Although the expression of CKs 8,18 and 14 varied among the tumors sub-types, a straight relationship between each histologic pattern and the CK expression could not be delineated. MSA was reactive in only three tumors while CKs 10 and 13 were not detected in any tumor studied. The absence of MSA and the expression of CKs 8,18 and 7, in most of the tumor cells, lead to the hypothesis that myoepithelial cells are not the major cellular component of the PLGA. TEM revealed cells exhibiting microvilli and variable amounts of secretory granules, some of them suggesting an excretory activity. The presence of CKs 8, 18 and 7, added to the secretory granules, indicates that PLGA originates from cells located at the acinar-intercalated duct junction. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:164 / 172
页数:9
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