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Prognostic significance of Ki-67 in great cell undifferentiated carcinoma of the major salivary glands: study of 11 cases

机译:Ki-67在主要涎腺大细胞未分化癌中的预后意义:11例研究

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INTRODUCTION: To establish the relation between the biologic behaviour and the prognosis of the undifferentatiated carcinoma of major salivary glands. OBJECTIVE: Identification of clinical histological, imunohistochemical parameters and its influence on the prognosis. STUDY DESIGN: Specimens analysis through histological and imunoihistochemical procedures. MATERIAL AND METHOD: Eleven cases of Undifferentiated Carcinoma of Major Salivary Glands were diagnosed and treated at the Head and Neck and Otorhinolaryngology Department of Hospital Heliópolis, Hosphel, São Paulo, from 1977 to 2000. These specimens were reviewed through histological and imunohistochemical procedures, and sub classified for positivity profile of citokeratines (high and low molecular weights). Then, it was defined a bi-directional pattern of histogenetic differentiation (mucoepidermoid type) and unidirectional pattern (epidermoid or ductal/glandular types), and its relation to clinic-demographic, mitotic index and cellular imunoproliferation (Ki- 67) clone MB-1, concerning to biological behaviour of these neoplasias. RESULTS: showed the predominance of patients withy more than 40 years old, white, parotid gland location and aggressiveness since early stages (T1 e T2). The mitotic and cellular imunoproliferative index (Ki-67) revealed values of high malignancy neoplasias (p0,01) as mucoepidemoid, cystic adenoid and acinar carcinoma. CONCLUSION: The imunohistochemical subclassification positivity for citokeratines, did not show statistical differences between mitotic and cellular imunoproliferative index (Ki-67), relating to predictive prognosis of these neoplasias.
机译:简介:建立生物学行为与主要唾液腺未分化癌的预后之间的关系。目的:确定临床组织学,免疫组化参数及其对预后的影响。研究设计:通过组织学和免疫组织化学方法进行标本分析。材料与方法:1977年至2000年,在圣保罗霍斯普尔医院Heliópolis医院的头颈和耳鼻咽喉科诊断并治疗了11例主要唾液腺未分化癌。对这些标本进行了组织学和免疫组织化学检查,子分类为citokeratines(高分子量和低分子量)的阳性特征。然后,它定义了组织遗传学分化的双向模式(粘液表皮样类型)和单向模式(表皮样或导管/腺样类型),及其与临床人口统计学,有丝分裂指数和细胞免疫增殖(Ki-67)克隆MB-的关系。关于这些瘤形成的生物学行为,参见图1。结果:显示自早期(T1 e T2)以来,年龄超过40岁,白人,腮腺位置和侵略性较高的患者。有丝分裂和细胞免疫增生指数(Ki-67)显示出高恶性肿瘤(p <0.01),如粘液表皮样,囊性腺样变和腺泡癌。结论:citokeratines的免疫组化亚分类阳性没有显示有丝分裂和细胞免疫增生指数(Ki-67)之间的统计学差异,与这些肿瘤的预后有关。

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