Stefan H, Semecký V
Department of Urology, Charles University, Faculty of Medicine, Hradec Králové.
Acta Medica (Hradec Kralove). 1998;41(1):29-33.
An incidence of bilateral gonadoblastoma in a 23-month old, mentally retarded boy with congenital sporadic aniridia, undescended dysgenetic testes, deletion of a chromosome (11) (p1302p14.2) and a later occurring unilateral Wilms' tumor is reported. The patient was treated by bilateral gonadectomy, nephrectomy, and chemotherapy, and is alive and well five years later. Another three aniridia/gonablastoma observations from the literature are discussed, two of them without and one in combination with Wilms' tumor. Diagnosis of gonadoblastoma remained unsuspected in two cases until autopsy and in another two cases it was done at surgery. A comparison of four cases reveals common finding--aniridia, dysgenetic gonads, genital abnormalities, mental retardation, deletion of 11p13, early occurrence and bilaterality of gonadoblastoma.
报告了一名23个月大、患有先天性散发性无虹膜、隐睾发育不全、11号染色体(p13.02p14.2)缺失且后来发生单侧肾母细胞瘤的智力发育迟缓男孩发生双侧性腺母细胞瘤的病例。该患者接受了双侧性腺切除术、肾切除术和化疗,五年后仍健在且状况良好。文中还讨论了文献中另外三例无虹膜/性腺母细胞瘤的观察病例,其中两例无肾母细胞瘤,一例合并肾母细胞瘤。在两例病例中,直到尸检时才怀疑性腺母细胞瘤的诊断,另外两例则在手术时确诊。对四例病例的比较揭示了一些共同发现——无虹膜、性腺发育不全、生殖器异常、智力发育迟缓、11p13缺失、性腺母细胞瘤的早期发生和双侧性。