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1.
Ann Diagn Pathol ; 19(5): 306-9, 2015 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26190154

RESUMEN

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.


Asunto(s)
Ameloblastoma/virología , ADN Viral/genética , Neoplasias Maxilomandibulares/virología , Papillomaviridae/genética , Infecciones por Papillomavirus/virología , Neoplasias de los Senos Paranasales/virología , Adolescente , Adulto , Anciano , Ameloblastoma/genética , Ameloblastoma/patología , Carcinoma de Células Escamosas/genética , Carcinoma de Células Escamosas/patología , Carcinoma de Células Escamosas/virología , Niño , ADN Viral/análisis , Femenino , Papillomavirus Humano 16/genética , Papillomavirus Humano 16/aislamiento & purificación , Humanos , Hibridación in Situ , Neoplasias Maxilomandibulares/genética , Neoplasias Maxilomandibulares/patología , Masculino , Persona de Mediana Edad , Papillomaviridae/aislamiento & purificación , Infecciones por Papillomavirus/genética , Infecciones por Papillomavirus/patología , Neoplasias de los Senos Paranasales/genética , Neoplasias de los Senos Paranasales/patología , Reacción en Cadena de la Polimerasa , Adulto Joven
2.
Ultrastruct Pathol ; 31(6): 393-400, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-18098057

RESUMEN

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.


Asunto(s)
Apoptosis , Neoplasias Maxilomandibulares/ultraestructura , Linfoma/ultraestructura , Biomarcadores de Tumor/análisis , Núcleo Celular/ultraestructura , Niño , Preescolar , Infecciones por Virus de Epstein-Barr/complicaciones , Infecciones por Virus de Epstein-Barr/patología , Femenino , Herpesvirus Humano 4/inmunología , Herpesvirus Humano 4/aislamiento & purificación , Humanos , Neoplasias Maxilomandibulares/química , Neoplasias Maxilomandibulares/mortalidad , Neoplasias Maxilomandibulares/virología , Linfoma/química , Linfoma/mortalidad , Linfoma/virología , Masculino , Mandíbula/patología , Maxilar/patología , Pronóstico , Tasa de Supervivencia
3.
Leuk Lymphoma ; 40(3-4): 405-11, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11426563

RESUMEN

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.


Asunto(s)
Neoplasias Abdominales/virología , Neoplasias de la Médula Ósea/virología , Linfoma de Burkitt/virología , Neoplasias Maxilomandibulares/virología , ARN Viral/genética , Neoplasias Abdominales/epidemiología , Neoplasias Abdominales/patología , Factores de Edad , Neoplasias de la Médula Ósea/epidemiología , Neoplasias de la Médula Ósea/patología , Linfoma de Burkitt/epidemiología , Linfoma de Burkitt/patología , Niño , Expresión Génica , Herpesvirus Humano 4/genética , Humanos , Hibridación in Situ , Israel/epidemiología , Neoplasias Maxilomandibulares/epidemiología , Neoplasias Maxilomandibulares/patología , Tasa de Supervivencia , Topografía Médica , Resultado del Tratamiento
6.
J Oral Maxillofac Surg ; 61(4): 467-70, 2003 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12684965

RESUMEN

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.


Asunto(s)
Ameloblastoma/virología , Neoplasias Maxilomandibulares/virología , Papillomaviridae/patogenicidad , Adolescente , Adulto , Estudios de Casos y Controles , Sondas de ADN de HPV , ADN Viral/análisis , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos
7.
J Oral Maxillofac Surg ; 58(10): 1129-34; discussion 1135-6, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11021708

RESUMEN

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.


Asunto(s)
Ameloblastoma/virología , Neoplasias Maxilomandibulares/virología , Papillomaviridae/aislamiento & purificación , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Southern Blotting , Distribución de Chi-Cuadrado , Sondas de ADN de HPV , ADN Viral/análisis , Electroforesis en Gel de Agar , Femenino , Humanos , Masculino , Persona de Mediana Edad , Reacción en Cadena de la Polimerasa
8.
Pathol Int ; 47(7): 449-53, 1997 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-9234383

RESUMEN

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.


Asunto(s)
Ameloblastoma/virología , Infecciones por Herpesviridae/virología , Herpesvirus Humano 4/patogenicidad , Enfermedades Maxilomandibulares/virología , Neoplasias Maxilomandibulares/virología , Quistes Odontogénicos/virología , Infecciones Tumorales por Virus/virología , Latencia del Virus , Adolescente , Adulto , Factores de Edad , Anciano , Niño , Femenino , Humanos , Hibridación in Situ , Masculino , Persona de Mediana Edad , ARN Viral/metabolismo , Estudios Retrospectivos , Factores Sexuales
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