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[成人睾丸生殖细胞肿瘤中滋养层成分的诊断、患病率、预后及治疗]

[Diagnosis, prevalence, prognosis and treatment of the trophoblastic component in germinal tumours of the testis in the adult].

作者信息

Ewald N, Roth A, Nezelof C, Cukier J

出版信息

J Urol (Paris). 1982;88(6):325-35.

PMID:6294186
Abstract

The authors report a series of 97 germinal tumours of the testis in the adult, studied first in terms of conventional histological data. Of 33 seminomas, 2 secreted HCG. The 5-year actuarial survival at stage I was 93%, and at stage II 75%. Stage II deaths revealed the existence of not purely seminomatous tumours. Amongst dysembryomas, half secreted HCG, with 3 histological groups: predominant choriocarcinomas, tumours with a trophoblastic component and "apparently pure" dysembryomas. The 3-year actuarial survival for dysembryomas was 90% at stage I and 58% at stage II. 51 patients of the series were studied retrospectively by sections with HCG peroxidase, a technique which reveals the intracytoplasmic synthesis of the hormone. Two types of cells have proved capable of such synthesis: syncytial cells, of syncytial-trophoblastic type, and small mononuclear cells. One third of seminomas and 90% of dysembryomas proved to have a trophoblastic component as demonstrated by HCG immunoperoxidases. All patients secreting HCG were HCG peroxidase positive. This equally applied to all patients with syncytial cells. Furthermore, all the indications are that HCG secretion is above all by the syncytial cells. From a diagnostic standpoint, any rise in beta HCG is synonymous with an HCG immunoperoxidase trophoblastic component. Detection of such a component using immunoperoxidase would seem to be essential for non-secreting tumours. From a prognostic standpoint, seminomas with a trophoblastic component are in fact dysembryomas and lymph node dissection should be performed, this being the only way of not missing a non-seminomatous metastasis. Therapeutically, pure seminomas are distinguished by the possibility of cure by radiotherapy. For all other tumours, orchidectomy must be followed by lymph node dissection. Subsequent treatment is decided on the basis of the results of the latter, with the exception of tumours with visceral metastases where chemotherapy must come first.

摘要

作者报告了一系列97例成人睾丸生殖细胞瘤,首先依据传统组织学数据进行研究。在33例精原细胞瘤中,2例分泌人绒毛膜促性腺激素(HCG)。Ⅰ期的5年精算生存率为93%,Ⅱ期为75%。Ⅱ期死亡病例显示存在非单纯精原细胞瘤。在胚胎癌中,一半分泌HCG,有3个组织学类型:以绒毛膜癌为主型、具有滋养层成分的肿瘤和“看似单纯”的胚胎癌。胚胎癌Ⅰ期的3年精算生存率为90%,Ⅱ期为58%。该系列中的51例患者通过HCG过氧化物酶切片进行回顾性研究,这是一种可揭示激素胞浆内合成的技术。已证实有两种细胞能够进行这种合成:合体滋养层型的合体细胞和小单核细胞。通过HCG免疫过氧化物酶证实,三分之一的精原细胞瘤和90%的胚胎癌有滋养层成分。所有分泌HCG的患者HCG过氧化物酶均呈阳性。这同样适用于所有有合体细胞的患者。此外,所有迹象表明,HCG主要由合体细胞分泌。从诊断角度看,β-HCG的任何升高都意味着存在HCG免疫过氧化物酶滋养层成分。对于不分泌的肿瘤,使用免疫过氧化物酶检测这种成分似乎至关重要。从预后角度看,具有滋养层成分的精原细胞瘤实际上是胚胎癌,应进行淋巴结清扫,这是不漏诊非精原细胞瘤转移的唯一方法。在治疗方面,单纯精原细胞瘤的特点是可通过放疗治愈。对于所有其他肿瘤,必须在睾丸切除术后进行淋巴结清扫。后续治疗根据淋巴结清扫结果决定,但有内脏转移的肿瘤除外,此类肿瘤必须首先进行化疗。

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