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双侧附睾乳头状囊腺瘤作为冯·希佩尔-林道综合征的一部分:一例以不育症表现的病例报告。

Bilateral papillary cystadenoma of the epididymis as a component of von Hippel-Lindau's syndrome: report of a case presenting as infertility.

作者信息

de Souza Andrade J, Bambirra E A, Bicalho O J, de Souza A F

出版信息

J Urol. 1985 Feb;133(2):288-9. doi: 10.1016/s0022-5347(17)48920-8.

Abstract

We report a case of bilateral papillary cystadenoma of the epididymis thought to be a component of the von Hippel-Lindau syndrome. The patient was hospitalized initially because of infertility. He had undergone a craniotomy 2 years previously for the diagnosis of a cerebellar hemangioblastoma. Funduscopy had revealed angiomatous lesions of the left eye. The von Hippel-Lindau syndrome is discussed briefly and the importance of long-term urological followup for possible presentation of silent renal carcinoma is emphasized. Patients with bilateral epididymal papillary cystadenoma are prone to have other components of the von Hippel-Lindau syndrome, and clinical studies are indicated in all such patients.

摘要

我们报告一例双侧附睾乳头状囊腺瘤,考虑为冯·希佩尔-林道综合征的一部分。患者最初因不育症住院。他在两年前因诊断为小脑成血管细胞瘤而接受了开颅手术。眼底检查发现左眼有血管瘤样病变。简要讨论了冯·希佩尔-林道综合征,并强调了长期进行泌尿外科随访以发现可能隐匿性肾癌的重要性。双侧附睾乳头状囊腺瘤患者易患冯·希佩尔-林道综合征的其他病变,所有此类患者均需进行临床研究。

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