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血管密度不能预测临床I期睾丸非精原细胞瘤未来的转移性疾病。

Vascular density does not predict future metastatic disease in clinical stage 1 non-seminomatous germ cell tumours of the testis.

作者信息

Maher T M, Lee A H

机构信息

University Department of Pathology, Southampton General Hospital, UK.

出版信息

Histopathology. 1998 Mar;32(3):217-24. doi: 10.1046/j.1365-2559.1998.00350.x.

Abstract

AIM

This study aimed to determine whether patients with stage 1 testicular non seminomatous germ cell tumours (NSGCT) with high vascular density have a greater risk of disease recurrence than those with a low vascular density.

METHODS AND RESULTS

Orchidectomy specimens from 42 patients with stage 1 NSGCT, treated by orchidectomy and surveillance alone, were studied. Vessel density was counted in tumour sections immunohistochemically stained for CD34. The mean of the three highest counts (x250, field size 0.67 mm2) for each tumour was used. Tumour vessel density was very similar for relapsing and non relapsing patients. Vascular invasion was the only variable significantly predictive of disease recurrence at 2 years post-orchidectomy (P = 0.025). There was wide variation of vessel counts between different blocks of a tumour, compared with interobserver variation. The tumour tissue type in the area of highest vessel density was embryonal carcinoma in 50% and teratoma (mature or immature) in 38%.

CONCLUSIONS

We confirmed the value of vascular invasion as a prognostic marker in stage 1 NSGCT. Tumour vessel density was of no prognostic value. Two factors may contribute to this. First, there was wide variation of vessel density between different blocks of a tumour. Second, the most vascular area in a tumour was frequently in low-grade tumour.

摘要

目的

本研究旨在确定1期睾丸非精原细胞瘤(NSGCT)且血管密度高的患者与血管密度低的患者相比,疾病复发风险是否更高。

方法与结果

对42例仅接受睾丸切除术及监测的1期NSGCT患者的睾丸切除标本进行研究。在免疫组化染色为CD34的肿瘤切片中计数血管密度。使用每个肿瘤三个最高计数(×250,视野大小0.67平方毫米)的平均值。复发和未复发患者的肿瘤血管密度非常相似。血管侵犯是睾丸切除术后2年疾病复发的唯一显著预测变量(P = 0.025)。与观察者间差异相比,肿瘤不同区域之间的血管计数存在很大差异。血管密度最高区域的肿瘤组织类型中,50%为胚胎癌,38%为畸胎瘤(成熟或不成熟)。

结论

我们证实了血管侵犯作为1期NSGCT预后标志物的价值。肿瘤血管密度无预后价值。可能有两个因素导致此情况。第一,肿瘤不同区域之间的血管密度存在很大差异。第二,肿瘤中血管最丰富的区域通常为低级别肿瘤。

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