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1.
J Clin Pathol ; 63(11): 1002-7, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20924089

ABSTRACT

OBJECTIVE: Salivary gland disorders in patients with chronic hepatitis C (CHC) have been considered oral extrahepatic manifestations, reinforcing the hepatitis C virus (HCV) as a sialotropic virus. Hence, the authors investigated the prevalence of HCV RNA in saliva and salivary glands and its possible association with xerostomia, hyposalivation and sialadenitis in patients with CHC. PATIENTS AND METHODS: In 65 patients with confirmed CHC, the HCV RNA was investigated by nested RT-PCR in saliva samples and minor salivary glands. Xerostomia, hyposalivation, clinical and histopathological evidence of sialadenitis were also evaluated. Univariate and multivariate analyses were employed to verify associations. RESULTS: HCV RNA was detected in the saliva of 26/65 (40.0%) patients and in 12/65 (18.5%) salivary glands. Xerostomia was reported by 23/65 (35.4%) patients, and hyposalivation was diagnosed in 13/65 (20.0%) patients. Sialadenitis was confirmed by histopathological features in 31/65 (47.7%) patients. Twelve (38.7%) of the 31 patients with sialadenitis presented HCV RNA in saliva and 2/31 (6.5%) in salivary glands. No associations were found between xerostomia, hyposalivation or sialadenitis and the detection of HCV RNA in saliva or in salivary glands. CONCLUSIONS: Although xerostomia, hyposalivation and sialadenitis are frequent findings in CHC patients, our study did not confirm the association between the detection of HCV RNA in saliva or salivary glands with these salivary gland disorders. However, an indirect role of HCV by immune-mediated virus mechanisms in the pathogenesis of salivary gland disorders in this group of patients cannot be ruled out.


Subject(s)
Hepacivirus/isolation & purification , Hepatitis C, Chronic/complications , Saliva/virology , Sialadenitis/virology , Xerostomia/virology , Adolescent , Adult , Aged , Cross-Sectional Studies , Female , Hepatitis C, Chronic/pathology , Humans , Male , Middle Aged , RNA, Viral/analysis , Reverse Transcriptase Polymerase Chain Reaction/methods , Salivary Glands, Minor/pathology , Salivary Glands, Minor/virology , Sialadenitis/pathology , Xerostomia/pathology , Young Adult
2.
Oral Dis ; 13(3): 329-34, 2007 May.
Article in English | MEDLINE | ID: mdl-17448218

ABSTRACT

INTRODUCTION: Chronic graft-vs-host disease (cGVHD) is a major cause of morbidity in long-term survivors of allogeneic hematopoietic progenitor cell transplantation. Herpesviruses are involved in the occurrence and progression of various oral diseases. AIM: The aim of this study was to investigate the role of human herpesvirus 6 (HHV6) in patients with oral manifestations of cGVHD. MATERIALS AND METHODS: Peripheral blood and oral fluids (whole saliva, gingival crevicular fluid and parotid gland saliva) from 19 cGVHD patients, and 28 blood donors were examined for HHV6. Oral tissue samples were collected from 12 cGVHD patients and 12 healthy individuals. Nested polymerase chain reaction was employed to identify the HHV6. RESULTS AND CONCLUSION: The virus was detected in whole saliva in 13 cGVHD patients (68%) and in 19 blood donors (67%). HHV6 was not identified in any of the gingival crevicular fluid and parotid gland saliva samples in cGVHD patients. In the control group 14.3% of both, four gingival crevicular fluid and four parotid gland saliva samples were positive. Two oral tissue samples of cGVHD patients were positive for HHV6. These results indicate that patients with oral manifestations of cGVHD and healthy individuals present high and similar incidence of HHV6 in blood and oral fluids. These data do not support the importance of HHV6 in oral lesions of cGVHD.


Subject(s)
Graft vs Host Disease/virology , Hematopoietic Stem Cell Transplantation/adverse effects , Herpesvirus 6, Human/pathogenicity , Mouth Diseases/virology , Adult , Case-Control Studies , DNA, Viral/analysis , Female , Gingival Crevicular Fluid/virology , Graft vs Host Disease/etiology , Humans , Lichen Planus, Oral/etiology , Lichen Planus, Oral/virology , Male , Middle Aged , Mouth Diseases/etiology , Mouth Mucosa/virology , Oral Ulcer/etiology , Oral Ulcer/virology , Saliva/virology , Salivary Glands, Minor/virology
3.
J Oral Pathol Med ; 32(7): 431-7, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12846790

ABSTRACT

BACKGROUND: The diffuse infiltrative lymphocytosis syndrome (DILS) in HIV patients is characterized by the persistence of CD8-circulating lymphocytes and lymphocytic infiltration, predominantly in salivary glands. METHODS: We examined seven HIV-positive patients with bilateral parotid enlargement and sicca symptoms. Minor labial salivary gland biopsies were performed in all patients and submitted for histopathological analysis and immunohistochemistry for CD4, CD8, cytomegalovirus (CMV), LMP-EBV protein, and HIV p-24 protein. RESULTS: In all cases, lymphocytic infiltration of the minor salivary glands, mainly periductal, was found. Acinar atrophy, ductal ectasia, and mild to moderate fibrosis were also observed. We noticed strong immunohistochemical reaction for LMP-EBV and p-24 proteins in ductal cells in all cases, while staining for CMV was consistently negative. The lymphocytes were positive for CD8, but consistently negative for CD4. CONCLUSIONS: A role of Epstein-Barr virus (EBV) and HIV, but not CMV, in the pathogenesis of DILS, is suggested by our immunohistochemical findings.


Subject(s)
Cytomegalovirus/isolation & purification , HIV Core Protein p24/analysis , HIV Infections/pathology , Herpesvirus 4, Human/isolation & purification , Lymphocytosis/pathology , Salivary Gland Diseases/pathology , Salivary Glands, Minor/pathology , Adult , Antigens, Viral/analysis , CD4-Positive T-Lymphocytes/pathology , CD8-Positive T-Lymphocytes/pathology , Capsid/ultrastructure , Female , HIV Infections/virology , Humans , Lymphocytosis/virology , Male , Middle Aged , Parotid Diseases/pathology , Parotid Diseases/virology , Salivary Ducts/pathology , Salivary Ducts/virology , Salivary Gland Diseases/virology , Salivary Glands, Minor/virology , Syndrome , Viral Matrix Proteins/analysis , Xerostomia/pathology , Xerostomia/virology
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