Expression of beta-human chorionic gonadotropin (beta-hCG) in non-trophoblastic elements of transitional cell carcinoma of the bladder: possible relationship with the prognosis.

Revista paulista de medicina Pub Date : 1993-05-01
C E Bacchi, K I Coelho, J Goldberg
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Abstract

Transitional cell carcinoma (TCC) of the bladder is a neoplasm with variability in its clinical behavior. Although there are several studies correlating stage and ABO isoantigen expression with invasiveness, there is no single predictor factor to assess the potential invasiveness, especially in the low grade, non-invasive TCC. In the present study we evaluated the correlation of histological grade plus stage and the expression of beta human chorionic gonadotropin (beta-hCG), in 100 cases of TCC, with the clinical behavior. These features were correlated with tumor progression in patients with at least two years of follow up. We observed more aggressiveness in G4 group (high grade and invasive) (93% had tumor progression) when compared to G1 group (low grade and superficial) (11% had tumor progression). However in 25.5% of the TCC cases (groups G2: low grade and invasive and G3: high grade and superficial) the clinical behavior was intermediate, showing some limitation in using grading and staging only, as a predictive factor. There was an expression of beta-hCG in 21.4% of the cases in up to 25% of the tumor cells without any trophoblastic morphology. These beta-hCG producing TCC had a strong correlation with aggressiveness: 39.1% and 12.8% of the TCC expressed beta-hCG with and without tumor progression, respectively.

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β -人绒毛膜促性腺激素(β - hcg)在膀胱移行细胞癌非滋养细胞成分中的表达:与预后的可能关系
膀胱移行细胞癌(TCC)是一种临床表现多变的肿瘤。虽然有一些研究将分期和ABO同抗原表达与侵袭性联系起来,但没有单一的预测因素来评估潜在的侵袭性,特别是在低级别、非侵袭性TCC中。在本研究中,我们评估了100例TCC的组织学分级加分期和β -人绒毛膜促性腺激素(β - hcg)的表达与临床行为的关系。这些特征与随访至少两年的患者的肿瘤进展相关。我们观察到G4组(高级别和侵袭性)(93%有肿瘤进展)比G1组(低级别和浅表)(11%有肿瘤进展)更具侵袭性。然而,在25.5%的TCC病例中(G2组:低分级和侵袭性,G3组:高分级和浅表性),临床行为处于中等水平,仅将分级和分期作为预测因素存在一定的局限性。21.4%的病例在高达25%的无滋养层形态的肿瘤细胞中有β - hcg的表达。这些产生β - hcg的TCC与侵袭性有很强的相关性:分别有39.1%和12.8%的TCC在肿瘤进展和未进展时表达β - hcg。
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