Attard-Montalto S P, Schuller I, Lastowska M A, Gibbons B, Kingston J E, Eden O B
Department of Paediatric Oncology, St. Bartholomew's Hospital, West Smithfield, London, United Kingdom.
Pediatr Hematol Oncol. 1994 Mar-Apr;11(2):197-200. doi: 10.3109/08880019409141656.
Patients with a 47, XXY karyotype (Klinefelter syndrome) appear to have an increased risk of developing a malignancy in adulthood, usually cancer of the breast, extragonadal germ cell tumor, and acute nonlymphoblastic leukemia. There is growing evidence to show that these patients also have an increased risk of developing a malignancy in childhood. There are reports describing the development of acute lymphoblastic leukemia, retinoblastoma, and rhabdomyosarcoma in children with a 47, XXY or mosaic 47, XXY/46, XY karyotype. We report a child with a bone metastasizing, B-cell lineage, non-Hodgkin's lymphoma (NHL) who was found to have a 47, XXY karyotype in both the tumor and constitutional cells.
核型为47, XXY(克兰费尔特综合征)的患者在成年期患恶性肿瘤的风险似乎增加,通常是乳腺癌、性腺外生殖细胞瘤和急性非淋巴细胞白血病。越来越多的证据表明,这些患者在儿童期患恶性肿瘤的风险也会增加。有报告描述了核型为47, XXY或嵌合型47, XXY/46, XY的儿童发生急性淋巴细胞白血病、视网膜母细胞瘤和横纹肌肉瘤的情况。我们报告了一名患有骨转移的B细胞系非霍奇金淋巴瘤(NHL)的儿童,其肿瘤细胞和体细胞的核型均为47, XXY。