Pradhan Dinesh, Kaman Lileswar, Dhillon Jasreman, Mohanty Sambit K
Department of Pathology and Laboratory Medicine, Pushpanjali Crosslay Hospital, Delhi, India.
J Cancer Res Ther. 2015 Oct-Dec;11(4):1034. doi: 10.4103/0973-1482.150697.
Klinefelter syndrome (KS) is a well-documented abnormality of the sex chromosome, with an incidence of 1 in 600 newborn males. It is characterized by a 47, XXY or a mosaic karyotype, hypergonadotrophic hypogonadism, infertility, reduced body hair, gynecomastia, and tall stature. Different neoplasms such as breast, testicular, and lymphoreticular malignancies may occur in 1% to 2% of the cases with KS. Herein we describe a case of mediastinal mixed germ cell tumor (GCT) in a 40-year-old male with KS. Interestingly, this case also had mitral valve prolapse, and an incidental papillary microcarcinoma of the thyroid gland. In view of the presence of pulmonary nodules, antemortem differential diagnoses considered were mycobacterial infection, lymphoma, thymic carcinoma, and a primary/metastatic neoplasm of the lung. As GCT was not considered, the serum markers of a GCT were not performed. The diagnosis of this rare mediastinal mixed GCT with KS was made at autopsy.
克兰费尔特综合征(KS)是一种有充分文献记载的性染色体异常疾病,在新生儿男性中的发病率为1/600。其特征为47, XXY核型或嵌合核型、高促性腺激素性性腺功能减退、不育、体毛减少、乳腺增生和身材高大。在1%至2%的KS病例中可能会发生不同的肿瘤,如乳腺、睾丸和淋巴网状系统恶性肿瘤。在此,我们描述一例40岁患有KS的男性纵隔混合性生殖细胞肿瘤(GCT)。有趣的是,该病例还患有二尖瓣脱垂以及甲状腺偶然发现的乳头状微癌。鉴于存在肺结节,生前考虑的鉴别诊断包括分枝杆菌感染、淋巴瘤、胸腺癌以及肺部原发性/转移性肿瘤。由于未考虑GCT,未进行GCT的血清标志物检测。该例罕见的合并KS的纵隔混合性GCT是在尸检时确诊的。