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1.
Arch Pathol Lab Med ; 143(4): 424-431, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30500298

RESUMO

The International Collaboration on Cancer Reporting was established to internationally unify and standardize the pathologic reporting of cancers based on collected evidence, as well as to allow systematic multi-institutional intercountry data collection to guide cancer care in the future. This data set has been developed by the collaborative efforts of an international multidisciplinary panel of experts involved in the care of patients with carcinomas of the nasal cavity and paranasal sinuses (sinonasal tract). The nasal cavity and paranasal sinuses (including frontal, sphenoid, ethmoid, and maxillary sinuses) comprise a very complex anatomic area of the head and neck, affected by a sometimes bewildering array of neoplasms. Management of malignancies in this anatomic region involves complex surgery because of the anatomic confines and close proximity to many vital structures. Given a multidisciplinary approach, the standardized reporting of the carcinomas that develop in this anatomic region include both required (core) and recommended (noncore) elements in pathology reporting in order to be able to identify critical prognostic factors, often requiring clinical and radiologic correlation. A summary of the International Collaboration on Cancer Reporting guidelines and clinically relevant elements, along with additional explanatory notes, are provided, based on evidentiary support from the literature, set in the context of practical application.


Assuntos
Carcinoma/patologia , Conjuntos de Dados como Assunto , Neoplasias Nasais/patologia , Neoplasias dos Seios Paranasais/patologia , Guias de Prática Clínica como Assunto , Conjuntos de Dados como Assunto/normas , Humanos , Patologia Clínica/normas , Projetos de Pesquisa/normas
2.
Contemp Oncol (Pozn) ; 21(4): 267-273, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29416431

RESUMO

Chordomas are rare and low-grade malignant solid tumours, despite their histologically benign appearance, that arise in the bone from embryonic notochordal vestiges of the axial skeleton, a mesoderm-derived structure that is involved in the process of neurulation and embryonic development. Chordomas occurring in the skull base tend to arise in the basiocciput along the clivus. Three major morphological variants have been described (classical, chondroid, and atypical/dedifferentiated). The pathogenesis and molecular mechanisms involved in chordoma development remain uncertain. From a pathological standpoint, the microenvironment of a chordoma is heterogeneous, showing a dual epithelial-mesenchymal differentiation. These tumours are characterised by slow modality of biologic growth, local recurrence, low incidence of metastasis rates, and cancer stem cell (CSC) phenotype. The main molecular findings are connected with brachyury immunoexpression and activation of the downstream Akt and mTOR signalling pathways. The differentiation between typical and atypical chordomas is relevant because the tumoural microenvironment and prognosis are partially different. This review provides an insight into the recent and relevant concepts and histochemical markers expressed in chordomas, with special emphasis on dedifferentiated chordomas and their prognostic implications.

3.
Cell Oncol (Dordr) ; 35(4): 259-67, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22718136

RESUMO

BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is a tumour type that generally carries very complex chromosomal aberrations. An interesting feature is the elevated occurrence (58 %) of whole arm translocations and isochromosomes, resulting from breakage and illegitimate recombination in centromeric or pericentromeric regions. We hypothesized that alterations in DNA methylation may play a role in the breakage of centromeric repeat sequences in these tumours. METHODS: We studied the DNA methylation status of global repeats (LINE-1), subtelomeric repeats (D4Z4) and centromeric repeats (SAT-α) in relation to centromeric instability in a series of HNSCC cancer cell lines and primary tumours. We analysed the methylation status by pyrosequencing and the chromosomal aberrations by microarray CGH. RESULTS: We found a significant association between centromeric instability and hypomethylation of LINE-1, but not D4Z4 and SAT-α. CONCLUSION: These data suggest that centromeric instability is associated with genomic DNA hypomethylation only when occurring at specific DNA repeat sequences.


Assuntos
Metilação de DNA , Neoplasias de Cabeça e Pescoço/genética , Elementos Nucleotídeos Longos e Dispersos/genética , Sequências Repetitivas de Ácido Nucleico/genética , Idoso , Idoso de 80 Anos ou mais , Linhagem Celular Tumoral , Centrômero/genética , Aberrações Cromossômicas , Hibridização Genômica Comparativa , Neoplasias de Cabeça e Pescoço/patologia , Humanos , Cariotipagem , Masculino , Pessoa de Meia-Idade , Análise de Sequência de DNA
4.
Otolaryngol Head Neck Surg ; 140(3): 375-80, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19248946

RESUMO

OBJECTIVE: To determine the usefulness of specific and reliable serum biomarkers to predict cervical lymph node metastasis. METHODS: A cross-sectional study of cases and controls. Thirty-nine serum samples of head and neck squamous cell carcinoma were collected from patients during neoplasm resection. Another 10 serum samples were collected from healthy individuals as a control group. Selected serum biomarkers were E-cadherin, MMP-2, MMP-9, active MMP-13, and p53 autoantibodies. RESULTS: We found a correlation between active MMP-13 (>685 pg/mL; ROC curve analysis 95% CI for sensitivity 79.6-99.3; specificity 49.2-95.1; positive predictive value 65-100; and negative predictive value 36-100) as well as the presence of p53 autoantibodies and lymph node metastasis. Multimarker analysis using MMP-13 and p53 autoantibodies together provided better sensitivity (76%) and specificity (100%). CONCLUSIONS: The combined determination of active MMP-13 and p53 autoantibodies could improve diagnosis of lymphatic metastasis in head and neck squamous cell carcinoma and aid therapeutic decision making.


Assuntos
Biomarcadores Tumorais/sangue , Carcinoma de Células Escamosas/diagnóstico , Neoplasias de Cabeça e Pescoço/diagnóstico , Metaloproteinase 13 da Matriz/sangue , Caderinas/sangue , Carcinoma de Células Escamosas/sangue , Carcinoma de Células Escamosas/mortalidade , Carcinoma de Células Escamosas/cirurgia , Estudos Transversais , Neoplasias de Cabeça e Pescoço/sangue , Neoplasias de Cabeça e Pescoço/mortalidade , Neoplasias de Cabeça e Pescoço/cirurgia , Humanos , Metástase Linfática , Metaloproteinase 2 da Matriz/sangue , Metaloproteinase 9 da Matriz/sangue , Prognóstico , Curva ROC , Sensibilidade e Especificidade , Proteína Supressora de Tumor p53/imunologia
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