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1.
Ann Diagn Pathol ; 19(5): 306-9, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26190154

ABSTRACT

Human papillomavirus (HPV) has been associated with a variety of head and neck neoplasms, including squamous cell carcinomas and Schneiderian papillomas. Ameloblastomas can arise from either the gnathic bones or peripheral soft tissues. Peripheral sinonasal ameloblastomas share clinical features with Schneiderian papillomas. A small number of reports have described detection of HPV DNA within ameloblastomas. However, Most of these cases was reported in the 1990s, used the polymerase chain reaction technique, and only examined gnathic tumors. The current study was designed to determine whether low- or high-risk HPV DNA could be detected in gnathic or peripheral ameloblastomas using in situ hybridization. Twenty-nine examples of gnathic osseous and peripheral head and neck ameloblastomas were obtained from the authors' archives (University of Virginia and the Johns Hopkins Hospital). High-risk HPV DNA was not detected in any of the 29 tumors analyzed. Low-risk HPV DNA was identified in only 1 tumor, which was peripheral in origin, and from an immunocompromised patient. We believe that the HPV in this case represents a background "passenger" infection. This study demonstrates that HPV of either high- or low-risk subtypes is unlikely to play a role in the pathogenesis of sinonasal ameloblastomas.


Subject(s)
Ameloblastoma/virology , DNA, Viral/genetics , Jaw Neoplasms/virology , Papillomaviridae/genetics , Papillomavirus Infections/virology , Paranasal Sinus Neoplasms/virology , Adolescent , Adult , Aged , Ameloblastoma/genetics , Ameloblastoma/pathology , Carcinoma, Squamous Cell/genetics , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/virology , Child , DNA, Viral/analysis , Female , Human papillomavirus 16/genetics , Human papillomavirus 16/isolation & purification , Humans , In Situ Hybridization , Jaw Neoplasms/genetics , Jaw Neoplasms/pathology , Male , Middle Aged , Papillomaviridae/isolation & purification , Papillomavirus Infections/genetics , Papillomavirus Infections/pathology , Paranasal Sinus Neoplasms/genetics , Paranasal Sinus Neoplasms/pathology , Polymerase Chain Reaction , Young Adult
2.
Ultrastruct Pathol ; 31(6): 393-400, 2007.
Article in English | MEDLINE | ID: mdl-18098057

ABSTRACT

Research on ultrastructural cytopathological changes and apoptosis that occur in jaw lymphoma were done by using electron microscopy and ground sections. The author described this tumor in 1977-1978 as a highly malignant and lethal condition affecting children between 2 and 8 years (mean age 5 years). A duration of illness between 2 and 3 weeks is common and with a general condition of severe toxicity, anemia, and high body temperature. Clinical and pathological features of 24 children with jaw lymphoma seen in the Maxillofacial Unit, Surgical Specialized Hospital, Medical city, Baghdad, are described. Thirteen males and 11 females were included, with a death rate at 91.1%. The morphological characteristics were examined by ground sections. Lymphoblastic lymphoma features were observed and apoptotic changes were seen in some of the cells. Electron microscopy showed a high number of mitotic figures and lymphoblast transformation to plasma cells with high nucleo-cytoplasmic ratio. Some cells had double nuclei and some nuclei were more convoluted. Apoptotic changes were seen in some cells; chromatin clumps aggregated near the nuclear membrane. Cytoplasmic processes and mitochondria showing degeneration and virus-like particles were seen in both nuclei and cytoplasm. The presence of a high mitotic figure with active oncogenic virus growth and reduced apoptosis is a poor prognostic feature in jaw lymphoma.


Subject(s)
Apoptosis , Jaw Neoplasms/ultrastructure , Lymphoma/ultrastructure , Biomarkers, Tumor/analysis , Cell Nucleus/ultrastructure , Child , Child, Preschool , Epstein-Barr Virus Infections/complications , Epstein-Barr Virus Infections/pathology , Female , Herpesvirus 4, Human/immunology , Herpesvirus 4, Human/isolation & purification , Humans , Jaw Neoplasms/chemistry , Jaw Neoplasms/mortality , Jaw Neoplasms/virology , Lymphoma/chemistry , Lymphoma/mortality , Lymphoma/virology , Male , Mandible/pathology , Maxilla/pathology , Prognosis , Survival Rate
4.
J Oral Maxillofac Surg ; 61(4): 467-70, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12684965

ABSTRACT

PURPOSE: The purpose of this study was to determine the relation of ameloblastoma with one of its probable etiologic factors, human papilloma virus (HPV). MATERIALS AND METHODS: This study was carried out in a retrospective, observational, and blind manner with information forms using an exact polymerize chain reaction. Fifty paraffinated blocks of ameloblastoma tumor were compared with 50 impacted third molar follicles. RESULTS: The results indicate that statistically the incidence of HPV positivity in the case group is significantly higher than that in the control group (P <.025). Furthermore, in determination of trace HPV type in HPV-positive samples, the incidence of type 6 HPV in the case group is significantly higher than that in the control group (P <.005). None of types 8, 11, 16, 18, 31, and 33 were observed. CONCLUSION: The results of this research conclude that HPV could be regarded as a possible etiologic factor of ameloblastoma.


Subject(s)
Ameloblastoma/virology , Jaw Neoplasms/virology , Papillomaviridae/pathogenicity , Adolescent , Adult , Case-Control Studies , DNA Probes, HPV , DNA, Viral/analysis , Female , Humans , Male , Middle Aged , Retrospective Studies
6.
Leuk Lymphoma ; 40(3-4): 405-11, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11426563

ABSTRACT

We have analyzed paraffin sections from 32 children with histologically confirmed Burkitt's Lymphoma (BL) for the presence of EBV using in situ hybridization to detect expression of the EBV-encoded early RNAs (EBERs). EBV was present in the tumors of 11 patients (34%). Sixty nine percent of the children presented with abdominal disease, 19% had bone marrow infiltration and only one child had jaw involvement. There was no statistically significant difference between EBV positive and EBV negative children with regard to age, gender, origin, primary site at presentation, or clinical stage of disease. However, there was a trend for younger age in the children with EBV positive BL with a median age of 4, compared to 7 years in children with EBV negative BL. None of the 7 children of Ashkenazi Jewish origin had EBER positive disease. There was no difference in the treatment outcome between the EBV positive patients (estimated survival at 24 months of 82%) and EBV negative children (estimated survival rate of 71% (p=0.58)). In conclusion, although this is only a small series it seems that childhood BL in Israel has the clinical characteristics of sporadic, non-African type with 34% EBV association and a low incidence of jaw tumors. Our data suggest that Ashkenazi Jewish children with BL are less likely to have EBV positive tumors than other ethnic groups. However, more patients will need to be studied in order to assess the validity of this observation.


Subject(s)
Abdominal Neoplasms/virology , Bone Marrow Neoplasms/virology , Burkitt Lymphoma/virology , Jaw Neoplasms/virology , RNA, Viral/genetics , Abdominal Neoplasms/epidemiology , Abdominal Neoplasms/pathology , Age Factors , Bone Marrow Neoplasms/epidemiology , Bone Marrow Neoplasms/pathology , Burkitt Lymphoma/epidemiology , Burkitt Lymphoma/pathology , Child , Gene Expression , Herpesvirus 4, Human/genetics , Humans , In Situ Hybridization , Israel/epidemiology , Jaw Neoplasms/epidemiology , Jaw Neoplasms/pathology , Survival Rate , Topography, Medical , Treatment Outcome
7.
J Oral Maxillofac Surg ; 58(10): 1129-34; discussion 1135-6, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11021708

ABSTRACT

PURPOSE: This study investigated the possibility that human papilloma virus (HPV) is a possible etiologic agent in the development of ameloblastoma. MATERIALS AND METHODS: DNA was extracted from 18 formalin-fixed, paraffin-embedded biopsy specimens and assayed for the presence of HPV DNA by PCR using the L1 consensus primer and specific primers for HPV types 6/11, 16 and 18. RESULTS: Eight samples (67%) were positive for HPV. Of the 8 HPV-positive samples, 7 were positive for HPV 18. Four of the HPV 18-positive samples were also positive for HPV 6/11. One HPV-positive sample was not positive for any of the type-specific primers. CONCLUSIONS: No conclusions can be drawn about the etiologic role of HPV from this study, but surgical manipulation is suggested to be one of the reasons for HPV presence attributable to contamination from the surface mucosal epithelium in these tumors.


Subject(s)
Ameloblastoma/virology , Jaw Neoplasms/virology , Papillomaviridae/isolation & purification , Adolescent , Adult , Aged , Aged, 80 and over , Blotting, Southern , Chi-Square Distribution , DNA Probes, HPV , DNA, Viral/analysis , Electrophoresis, Agar Gel , Female , Humans , Male , Middle Aged , Polymerase Chain Reaction
8.
Pathol Int ; 47(7): 449-53, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9234383

ABSTRACT

In order to investigate the relationship between Epstein-Barr virus (EBV) latent infection and histogenesis of odontogenic disorders, in situ hybridization for EBV-encoded small RNA (EBER) was applied to the paraffin sections of ameloblastoma, dentigerous cyst, and odontogenic keratocyst. Eight cases (15%) of 53 ameloblastomas showed scattered signals for EBER in the parenchymal cells, whereas no reaction of EBER transcript was observed in the non-neoplastic cystic lesions. In the ameloblastoma, the follicular and plexiform types revealed the signals in the nuclei, but cystic, acanthomatous, granular, and basal cell types exhibited no reaction with EBER. The distribution of the signals without monoclonarity indicated that ameloblastoma cells may exclude EBV genomes or inactivate EBER-encoded genes. The results suggested that EBV participates as one of the transforming factors in the occurrence of ameloblastoma.


Subject(s)
Ameloblastoma/virology , Herpesviridae Infections/virology , Herpesvirus 4, Human/pathogenicity , Jaw Diseases/virology , Jaw Neoplasms/virology , Odontogenic Cysts/virology , Tumor Virus Infections/virology , Virus Latency , Adolescent , Adult , Age Factors , Aged , Child , Female , Humans , In Situ Hybridization , Male , Middle Aged , RNA, Viral/metabolism , Retrospective Studies , Sex Factors
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