bromochloroacetic-acid and Salivary-Gland-Diseases

In the present study we investigated tissue changes in palatine (PG) and labial (LG) minor salivary glands from individuals who had died of alcoholic hepatic cirrhosis, to characterize histopathological parameters of alcoholic sialosis, that may be used for differential diagnosis. Samples obtained from autopsies were processed using cytochemical techniques for mucosubstances and immunocytochemical labelling for cytokeratines, PS 100 and T-cells. Both PG and LG showed dilated excretory ducts with atrophic epithelium, which contained PAS+ metachromatic material and detached cells. Intra and interlobular ductal hyperplasia was present in some areas, mainly in PG. CK expression was heterogeneous in ductal cells, and negative in acinar cells. Most of the acinar cell nuclei were normal, but some of them were atypical in shape and distribution. Myoepithelial cells, serous demilunes and the basal region of the cells of the striated ducts expressed PS 100. In PG, 85% of the mononuclear infiltrates expressed T-cell markers, whereas in LG only 40% of these cells were T-cells. These findings, in addition to other histopathological parameters seen in previous studies, may be used as indicators for differential diagnosis with other gland pathologies.

Topics: Aged; Alcoholism; Case-Control Studies; Diagnosis, Differential; Humans; Immunoenzyme Techniques; Keratins; Liver Cirrhosis, Alcoholic; Male; Middle Aged; S100 Proteins; Salivary Ducts; Salivary Gland Diseases; Salivary Glands, Minor; T-Lymphocytes

Concerning the hypothesis that distinct types of salivary gland cysts may be the starting point of a salivary gland tumour, a histological examination of 1,661 salivary gland cysts was performed in order to analyse the cell types and their proliferative activity. Epithelial alterations were found especially in salivary duct cysts of parotid gland and in mucous retention cysts of minor salivary glands. Characteristic cellular changes were epithelial metaplasias (goblet cells, clear cells, squamous cells) and focal epithelial proliferations with plump or papillary plaques projecting into the cyst lumen. Only in one case had a mucoepidermoid carcinoma developed in the wall of a parotid duct cyst. The epithelial metaplasia and focal proliferative activity in salivary duct cysts is comparable to similar alterations in odontogenic cysts as possible early manifestation of a tumour, especially of an ameloblastoma or mucoepidermoid carcinoma. The differential diagnosis of salivary duct cysts must take primarily cystadenomas and cystic mucoepidermoid carcinomas of well-differentiated type into account.

Topics: Carcinoma, Mucoepidermoid; Cell Division; Cystadenoma, Mucinous; Cystadenoma, Papillary; Cysts; Epithelium; Histocytochemistry; Humans; Keratins; Parotid Neoplasms; Retrospective Studies; Salivary Ducts; Salivary Gland Diseases

Duct-ligated submandibular and sublingual glands of rats were evaluated immunohistochemically for changes in keratin (MoAb 1164), actin, S-100 protein and rat-EGF (rEGF). Normal salivary glands were reactive for keratin, S-100 protein and rEGF in the granular convoluted tubule (GCT) and duct cells, and for actin in the myoepithelium. Submandibular glands showed a marked reduction of S-100 protein and rEGF staining following duct ligation, and no increased staining of proliferating epithelial cells of the late stage in duct ligated glands. Sublingual glands revealed no marked changes for actin staining in myoepithelial cells, irrespective of atrophic changes occurring in acinar and duct cells after duct ligation. Immunohistochemical patterns differed for each type of gland; changes associated with the obstructive lesion were more prominent in the submandibular gland.

Topics: Actins; Animals; Atrophy; Cytoplasmic Granules; Epidermal Growth Factor; Epithelium; Keratins; Ligation; Male; Rats; Rats, Wistar; S100 Proteins; Salivary Gland Diseases; Sublingual Gland; Submandibular Gland; Submandibular Gland Diseases; Time Factors

The binding pattern of antibodies against different cytokeratin (CK) polypeptides, tissue polypeptide antigen (TPA), carcinoembryonic antigen (CEA), lactoferrin (Lf), lysozyme (Ly) and secretory component (SC) in palatal glands (PSG) of long-term denture wearing patients has been studied to investigate immunohistochemically the localization of these marker proteins in normal PSG and in denture-induced sialadenitis of PSG. The study included palatal gland biopsies from 28 patients (15 f, 13 m; mean age 59 years), 17 of them with normal PSGs, 8 with focal obstructive sialadenitis, and 3 with diffuse sialadenitis. Presence of CK and TPA was found in all intra- and extraglandular salivary ducts, in the basophilic portions of acini, in some mucous acini, and in all atrophic acini. Increased expression of CEA and Lf was observed in inflammed areas of PSG which, on the other site, were devoid of Ly and SC. In the mucous acini of healthy PSG considerable basal Ly immunoreactivity was seen. SC was localized in almost all ductal cells and in some acinar cells. Appearance of Lf in the ductal cells of PSG indicates an early sign of palatal sialadenitis. Some distinctions in the expression pattern of the marker proteins between the mucous acini of major salivary glands and PSG point to differences in the functional activities of either group of salivary glands.

Topics: Denture, Complete, Upper; Female; Humans; Immunoenzyme Techniques; Immunohistochemistry; Keratins; Male; Middle Aged; Muramidase; Palate; Receptors, Cell Surface; Salivary Gland Diseases; Salivary Glands; Salivary Glands, Minor; Secretory Component; Sialadenitis

The immunoreactivity pattern for different monoclonal antibodies to cytokeratins and to vimentin in epimyoepithelial islands typical for glands of patients with Sjögren's syndrome has been compared with that of normal parotid gland tissue. Two types of epithelial island cells were observed: one had an intermediate filament protein pattern similar to that of ordinary duct epithelial cells of normal parotid gland. The other had an intermediate filament protein pattern typical of myoepithelial and/or basal duct cells in normal glands. Thus, we conclude that the islands are composed of a mixed population of gland cells on the basis of their content of cytokeratins or of cytokeratins and vimentin. These cells might originate from pluripotential reserve cells or from ordinary duct, myoepithelial and/or basal duct cells which may have undergone metaplasia.

Topics: Antibodies, Monoclonal; Epithelium; Fibroblasts; Humans; Immunohistochemistry; Keratins; Parotid Gland; Salivary Gland Diseases; Sialadenitis; Sjogren's Syndrome; Staining and Labeling; T-Lymphocytes; Vimentin

Immunofluorescent and immunoperoxidase labelling of normal and metaplastic human submandibular salivary glands with a battery of cytokeratin-specific monoclonal antibodies was carried out. Labelling with a broad spectrum cytokeratin antibody (KG 8.13), as well as with antibody to cytokeratin polypeptide No. 18 (Ks 18.18) was observed in all the epithelial elements of the gland. Polypeptide No. 19, however, was present in ductal cells only, sparing the acini and the associated myoepithelium. Antibody KS 8.58, specific for cytokeratins Nos. 13 and 16, selectively labelled basal cells along the large ducts. Examination of squamous metaplasia associated with chronic suppurative sialadenitis indicated that the metaplastic cells display the same cytokeratin profile as the normal ductal cells and are not labelled with antibodies KS 8.58 and KK 8.60 which usually stain normal and pathological stratified epithelia. The significance of these observations for the histogenesis of normal salivary glands, as well as for the development of the metaplastic process, is discussed.

Topics: Antibodies, Monoclonal; Child; Epithelium; Fluorescent Antibody Technique; Humans; Immunoenzyme Techniques; Keratins; Metaplasia; Microscopy, Fluorescence; Peptides; Salivary Gland Diseases; Sialadenitis; Submandibular Gland; Submandibular Gland Diseases

Lectin-binding profiles and keratin distribution in obstructive adenitis of human submandibular glands (SMGs) are reported and compared those of normal SMGs. Histologically, obstructive changes in the SMGs included acinar atrophy, duct-like structure formation in the early stage, and disappearance of acinar cells and dilation of ductal segments in the later, chronic stage. The following lectins were used: Con A (Glc, Man), PNA(Gal, GalNAc), RCA-I(Gal), DBA(GalNAc), SBA(Gal, Gal-NAc), UEA-I(alpha-L-Fuc) and WGA(GlcNAC, NeuNAc). Lectin staining in atrophic acinar cells was usually reduced except for SBA binding and was irregularly distributed in altered acinar and ductal epithelia. Binding of DBA and UEA-I lectins were particularly intense along the luminar borders of ductal segments in the lesions. Immunohistochemically detectable keratins were characterized by intense staining in atrophic acinar cells and in all the ductal segments, whereas normal acinar cells, either serous or mucous, were negative.

Topics: Chronic Disease; Humans; Immunoenzyme Techniques; Keratins; Lectins; Salivary Gland Diseases; Sialadenitis; Staining and Labeling; Submandibular Gland; Submandibular Gland Diseases