Fujimoto Y, Monden Y, Nakahara K, Kawashima Y
Jpn J Surg. 1985 May;15(3):221-4. doi: 10.1007/BF02469891.
We treated a patient with a benign mediastinal teratoma associated with Klinefelter's syndrome which was first thought to be a malignant germ cell tumor because of an anterior mass shadow, gynecomastia, atrophic testis and a high level of HCG. Chromosomal analysis showed a total of 47 XXY. Median sternotomy revealed a tumor originating from the right lobe of thymus. The postoperative course and 2 year follow-up have been uneventful.
我们治疗了一名患有良性纵隔畸胎瘤并伴有克兰费尔特综合征的患者。该患者最初因前纵隔肿块阴影、男性乳房发育、睾丸萎缩及人绒毛膜促性腺激素(HCG)水平升高而被认为是恶性生殖细胞肿瘤。染色体分析显示共有47条XXY染色体。经正中胸骨切开术发现肿瘤起源于胸腺右叶。术后过程及2年随访均无异常。