Reddy S R, Svec F, Richardson P
Department of Medicine, Louisiana State University School of Medicine, New Orleans 70112.
South Med J. 1991 Jun;84(6):773-5. doi: 10.1097/00007611-199106000-00026.
We believe this is the first reported case of seminoma in a patient with the 48,XXYY variant form of Klinefelter's syndrome. Moreover, the seminoma in this patient occurred in a normally descended testis. We report this case because patients with 48,XXYY Klinefelter's syndrome are often confined to institutions, where the diagnosis of testicular tumor may not be recognized as readily.
我们认为这是首例报道的患有48,XXYY变异型克兰费尔特综合征患者发生精原细胞瘤的病例。此外,该患者的精原细胞瘤发生于正常下降至阴囊的睾丸。我们报告此病例是因为患有48,XXYY克兰费尔特综合征的患者常被收治于医疗机构,在那里睾丸肿瘤的诊断可能无法被及时识别。