Tangshewinsirikul Chayada, Dulyaphat Wirada, Tim-Aroon Thipwimol, Parinayok Rachanee, Chareonsirisuthigul Takol, Korkiatsakul Veerawat, Waisayarat Jariya, Sirisreetreerux Pokket, Tingthanatikul Yada, Wattanasirichaigoon Duangrurdee
Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Division of Medical Genetics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
J Pediatr Genet. 2020 Dec;9(4):221-226. doi: 10.1055/s-0040-1713002. Epub 2020 Jun 17.
Most cases of Klinefelter syndrome (KS) have 47,XXY karyotype. We reported the first case of 46,XX/47,XXY KS whose genital ambiguity was detected prenatally with postnatal confirmation of the mosaicism and ovotesticular disorder of sex development (OT-DSD). The paternal origin of the extra X chromosome was identified using trio cytogenomic single-nucleotide polymorphism array. Additional 18 cases were also reviewed. The clinical presentation of 46,XX/47,XXY is age-dependent with two age peaks, including ambiguous genitalia during infancy and gynecomastia with or without cyclical hematuria and left scrotal pain and mass in adolescence. The 46,XX is the predominant karyotype both in peripheral blood and gonadal tissue. The risk of germ cell tumor is very high throughout life in these individuals. Individuals with 46,XX/47,XXY mosaicism should be treated more as OT-DSD other than a simple mosaic KS. A multidisciplinary approach and long-term monitoring are necessary.
大多数克兰费尔特综合征(KS)病例的核型为47,XXY。我们报告了首例46,XX/47,XXY KS病例,其生殖器模糊在产前被检测到,产后证实存在嵌合体和性发育的卵睾性障碍(OT-DSD)。使用三联体细胞基因组单核苷酸多态性阵列确定了额外X染色体的父源。还对另外18例病例进行了回顾。46,XX/47,XXY的临床表现与年龄相关,有两个年龄高峰,包括婴儿期生殖器模糊以及青春期乳腺增生伴或不伴周期性血尿和左侧阴囊疼痛及肿块。46,XX在外周血和性腺组织中都是主要的核型。这些个体终生患生殖细胞肿瘤的风险非常高。46,XX/47,XXY嵌合体个体应更多地被视为OT-DSD,而非单纯的嵌合型KS。多学科方法和长期监测是必要的。