Brown I R, Dunlap H J, Nizalik E, Schillinger J F
Department of Urology, Children's Hospital of Eastern Ontario, Ottawa, Canada.
Urology. 1995 Dec;46(6):863-6. doi: 10.1016/s0090-4295(99)80359-8.
We report the case of a tumor in an intra-abdominal cryptorchid testis of a 7-month-old male infant. Torsion of a testicular teratoma was confirmed by pathologic examination. A review was undertaken to identify and characterize other reports of prepubertal cryptorchid germ cell neoplasms.
Cases of testicular germ cell neoplasms in association with cryptorchidism in phenotypically normal males were identified through a MEDLINE search of the English literature and review of published bibliographies.
A total of 14 cases were identified with testis location provided in 12 patients. Half of the neoplasms were located in abdominal testis, and all of these were associated with torsion, although 2 of 6 patients were asymptomatic. Two patients had tumors in the contralateral normally descended testis. Teratoma was the most frequently encountered tumor type.
Characteristics of prepubertal cryptorchid testicular germ cell tumors reflect those seen in post-pubertal cryptorchid tumors in location but differ in histologic type. Possible pathogenesis is discussed. Follow-up was not provided in all cases although outcome appears to be good. We believe that these lesions are likely underreported.
我们报告一例7个月大男婴腹腔内隐睾发生肿瘤的病例。经病理检查确诊为睾丸畸胎瘤扭转。我们进行了一项综述,以识别和描述青春期前隐睾生殖细胞肿瘤的其他报告。
通过对英文文献进行MEDLINE检索并查阅已发表的参考文献,确定表型正常男性中与隐睾症相关的睾丸生殖细胞肿瘤病例。
共确定14例病例,其中12例患者提供了睾丸位置。一半的肿瘤位于腹腔内睾丸,所有这些病例均与扭转相关,尽管6例患者中有2例无症状。2例患者对侧正常下降的睾丸中有肿瘤。畸胎瘤是最常见的肿瘤类型。
青春期前隐睾睾丸生殖细胞肿瘤的特征在位置上反映了青春期后隐睾肿瘤的特征,但在组织学类型上有所不同。讨论了可能的发病机制。尽管所有病例的结果似乎都良好,但并非所有病例都提供了随访情况。我们认为这些病变可能报告不足。