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[男性假两性畸形中的睾丸肿瘤]

[Testicular tumors in male pseudohermaphroditism].

作者信息

Bobokhidze N V, Bronshteĭn M E, Golubeva I V, Iur'eva N P

出版信息

Probl Endokrinol (Mosk). 1984 Nov-Dec;30(6):28-34.

PMID:6514682
Abstract

The data are summarized on the incidence and morphofunctional characteristics of gonadal tumors in different varieties of false male hermaphroditism, namely the testicular feminization syndrome (marked and unmarked forms), demonstrable masculinization and dysgenesis and compared with the disease clinical manifestations. The two syndromes--testicular feminization (marked form) and dysgenesis were found to be associated with a high risk of cancer development. In the first case there develop sertolioma-like tumors and in the second one, tumors similar to gonocytoma and dysgerminoma. These tumors became malignant in rare cases, they did not recur or metastasize. The treatment schedule for such patients has been developed. It includes the removal of the tumor-affected gonads and transfer of the tumor-free gonads into subcutaneous abdominal or scrotal areas and administration (during castration) of continuous substitution hormonotherapy according to the sex chosen.

摘要

总结了不同类型假性男性假两性畸形(即睾丸女性化综合征,包括明显型和不明显型、可证实的男性化和发育不全)中性腺肿瘤的发病率及形态功能特征,并与疾病临床表现进行了比较。发现两种综合征——睾丸女性化(明显型)和发育不全与癌症发生的高风险相关。在第一种情况下会发生类支持细胞瘤,在第二种情况下会发生类似于生殖细胞瘤和无性细胞瘤的肿瘤。这些肿瘤在极少数情况下会恶变,不会复发或转移。已制定了此类患者的治疗方案。包括切除受肿瘤影响的性腺,将无肿瘤的性腺转移至腹部皮下或阴囊区域,并根据所选性别在去势期间进行持续替代激素治疗。

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