Lardennois B, El Hansa A, Bernier F, Birembaut P, Caron J, Lemaire P
J Urol (Paris). 1981;87(9):631-4.
The authors present the case of a patient with Klinefelter syndrome who, at the age of 36 years, developed a multifocal Leydig cell tumour of the right testicle, presenting as hematuria. After orchidectomy, the patient developed an identical tumour in the remaining testes. This curious case of a patient in whom the clinical and laboratory features of Klinefelterer's syndrome, were masked by the Leydig cell tumour and vice versa, is analyzed. Study of this case, and a review of the literature of the three cases published in the past, offer no definitive solution to the problem of the possible link between the Leydig cell tumour and the Klinefelter syndrome, but a prospective study protocol is suggested with such an aim in mind. More careful clinical and laboratory evaluation of populations of Klinefelter's syndrome and Leydig cell tumours should provide a solution. More routine therapy of Klinefelt syndrome should possibly avoid the development of complications in the form of testicular Leydig cell tumours by causing inhibition of useless and excessive pituitary actions by the administration of androgens immediately after puberty.
作者报告了一例克氏综合征患者的病例,该患者36岁时右侧睾丸发生多灶性间质细胞瘤,表现为血尿。睾丸切除术后,患者剩余睾丸又出现了同样的肿瘤。本文分析了这一奇特病例,其中克氏综合征的临床和实验室特征被间质细胞瘤掩盖,反之亦然。对该病例的研究以及对过去发表的三例相关文献的回顾,并未为间质细胞瘤与克氏综合征之间可能存在的联系这一问题提供明确解决方案,但提出了一项前瞻性研究方案。对克氏综合征患者群体和间质细胞瘤进行更仔细的临床和实验室评估应能找到解决办法。克氏综合征的更常规治疗可能通过在青春期后立即给予雄激素抑制无用且过度的垂体活动,从而避免睾丸间质细胞瘤形式的并发症发生。