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1.
Rev Esp Patol ; 55(2): 90-95, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35483774

RESUMEN

BACKGROUND: Odontogenic keratocysts (OKCs) and orthokeratinized odontogenic Cysts (OOCs) are distinct clinicopathological entities. OKC appears to behave in a way more similar to that of a neoplasm, such as ameloblastoma (AB). The aim of this study is to compare the influence of Ki-67, Cyclin D1 and COX-2 in the diagnosis and pathogenesis of OKC, OOC and AB. MATERIALS AND METHODS: A cross-sectional observational study of 41 samples was organized into 3 groups: (1) OKC n=22; (2) AB n=13 and (3) OOC n=6. Paraffin blocks were sectioned and stained with hematoxylin and eosin (H&E). Immunohistochemical study using Bond Polymer Refine Red Detection Kit, Leica, Wetzlar, Germany, was performed for the following antibodies: Ki-67, Cyclin D1 and COX-2. Double blind immunostaining was quantified subjectively. Staining: nuclear or cytoplasmic; nuclear (Ki-67 and Cyclin D1>5% positive) and cytoplasmic (COX-2; 1; 1-30 cytoplasm: 2; 31-60 cytoplasm; 3; 61-100 cytoplasm). Considering positive stained 61-100 cytoplasms. RESULTS: The expression of Ki-67 was higher in the OKC group than in the AB group (p<0.05). Cyclin D1 showed a higher expression in OKC vs. OOC and OKC vs. AB (p<0.05). Finally, expression of COX-2 was higher in OKC vs AB (p<0.05). CONCLUSIONS: COX-2, Ki-67 and Cyclin D1 show statistically significant differences between the groups, suggesting that they could be useful tools in the differential diagnosis between OKCs and OOC and a predictive indicator for their biologic behaviour. The higher expressions of these 3 markers of OKC vs AB highlight once more the aggressive behaviour of this now re-considered cystic lesion. These markers could prove useful in the choice of more aggressive surgical treatment in OKCs as their behaviour appears to be similar to that of a neoplasm.


Asunto(s)
Ameloblastoma , Quistes Odontogénicos , Ameloblastoma/patología , Estudios Transversales , Ciclina D1 , Ciclooxigenasa 2 , Humanos , Antígeno Ki-67
2.
Rev Esp Patol ; 52(4): 265-269, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31530412

RESUMEN

Two cases of oral pulse granuloma (OPG) or vegetable granuloma (VG) are presented, one of which was concomitant with an odontogenic keratocyst (OKC), which is an unusual finding. OKC is characterized by the presence of hyaline rings which include vessels, giant cells, other inflammatory cells and collagen fibres. There are two hypotheses as to its histogenesis: firstly, as a reaction to vegetable matter, such as legumes (thus the nomenclature "pulse" or edible seed) and secondly as a degenerative change in the vessel walls as a result of localized vasculitis. Due to the deceptive appearance of OPG, diagnosis can be challenging.


Asunto(s)
Granuloma de Cuerpo Extraño/patología , Granuloma de Células Gigantes/patología , Hialina/química , Quistes Odontogénicos/complicaciones , Adolescente , Colágeno/análisis , Diagnóstico Diferencial , Femenino , Células Gigantes/patología , Granuloma de Cuerpo Extraño/complicaciones , Granuloma de Cuerpo Extraño/diagnóstico , Granuloma de Cuerpo Extraño/cirugía , Granuloma de Células Gigantes/complicaciones , Granuloma de Células Gigantes/diagnóstico , Granuloma de Células Gigantes/cirugía , Histiocitos/patología , Humanos , Masculino , Persona de Mediana Edad , Quistes Odontogénicos/cirugía , Osteólisis/etiología , Polisacáridos/análisis , Recurrencia , Vasculitis/etiología
3.
Otolaryngol Head Neck Surg ; 156(4): 677-682, 2017 04.
Artículo en Inglés | MEDLINE | ID: mdl-28322111

RESUMEN

Objective To determine the presence of human papillomavirus (HPV) in head and neck squamous cell carcinoma, specifically in the larynx without the bias of other sublocations, and to describe the different serotypes of HPV and their impact on overall and disease-free survival after 10-year follow-up. Study Design Retrospective case series with chart review of ear, nose, and throat oncologic database. Setting Academic tertiary care hospital. Subjects A total of 123 samples of larynx squamous cell carcinoma were included, only from the glottis and treated only with surgery between 1977 and 2005. Methods DNA extraction was carried out by polymerase chain reaction, and subsequent visualization was performed in low-density arrays. Results were compared with histologic, clinicopathologic, and survival parameters, with a 10-year follow-up. Results HPV DNA was detected in 22.76% (n = 28) of the samples. Eleven genotypes were detected, 2 of which had never been described in the larynx (HPV43 and HPV62). No increasing trend of HPV was observed over time. HPV presence did not correlate with better survival during the follow-up. Smoking was proven as an independent factor in relation to the presence of HPV. Conclusion HPV may represent a notable factor in the development of a subset of laryngeal squamous cell carcinoma without significant influence on overall and disease-free survival. More studies, including oncogene transcription proteins, would be necessary to draw more relevant conclusions about the relevance of HPV infection in the larynx.


Asunto(s)
Carcinoma de Células Escamosas/virología , Neoplasias Laríngeas/virología , Papillomaviridae/clasificación , Carcinoma de Células Escamosas/mortalidad , ADN Viral/análisis , Estudios de Seguimiento , Humanos , Neoplasias Laríngeas/mortalidad , Papillomaviridae/genética , Papillomaviridae/aislamiento & purificación , Estudios Retrospectivos , Serogrupo , Análisis de Supervivencia
4.
Acta Cytol ; 47(3): 485-9, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12789937

RESUMEN

BACKGROUND: Neurothekeoma (NT) is a rare, benign neoplasm of soft parts with a distinctive histologic appearance. To our knowledge, the cytologic findings have not been described before. We present a case of NT with the cytologic features on fine needle aspiration cytology (FNAC). CASE: A 54-year-old female presented with a circumscribed nodule in the left breast. The lesion was evaluated by FNAC. The smears showed an abundant, metachromatic, myxoid matrix with fusiform and epithelioid cells, some binucleated or multinucleated, loose or in groups and sometimes forming concentric whorls. The lesion was removed, and the diagnosis of NT was made after histopathologic study. CONCLUSION: NT is an extremely rare neoplasm in the mammary region. Fusiform and epithelioid cells arranged in concentric whorls in a myxoid tumor of soft tissue are a distinctive characteristic of this neoplasm and can suggest the diagnosis.


Asunto(s)
Biopsia con Aguja/métodos , Mama/patología , Neurotecoma/patología , Neoplasias de los Tejidos Blandos/patología , Biomarcadores de Tumor/análisis , Mama/cirugía , Células Epitelioides/patología , Femenino , Humanos , Inmunohistoquímica , Persona de Mediana Edad , Neurotecoma/química , Neurotecoma/cirugía , Neoplasias de los Tejidos Blandos/química , Neoplasias de los Tejidos Blandos/cirugía , Vimentina/análisis
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