Central hypogonadism in Klinefelter syndrome: report of two cases and review of the literature

• Published in: Journal of endocrinological investigation 2021-03, Vol.44 (3), p.459-470
• Main Authors: Cangiano, Biagio, Indirli, Rita, Profka, Eriselda, Castellano, Elena, Goggi, Giovanni, Vezzoli, Valeria, Mantovani, Giovanna, Arosio, Maura, Persani, Luca, Borretta, Giorgio, Ferrante, Emanuele, Bonomi, Marco
• Format: Article
• Language: English
• Subjects: Anosmia; Coexistence; Endocrinology; Gonadotropins; Hypogonadism; Hypothalamus; Internal Medicine; Karyotypes; Klinefelter's syndrome; Literature reviews; Magnetic resonance imaging; Medicine; Medicine & Public Health; Metabolic Diseases; Next-generation sequencing; Original Article; Phenotypes; Pituitary; Pituitary (anterior); Pituitary hormones; Puberty; Testosterone
• ISSN: 1720-8386; 0391-4097; 1720-8386
• DOI: 10.1007/s40618-020-01324-3

Purpose Klinefelter syndrome (KS) is characterized by late adolescence/young adulthood onset of primary hypogonadism. Hypogonadotropic hypogonadism (HH), when congenital, is usually associated with absent/incomplete puberty and low/normal gonadotropins. We report the clinical and genetic features of two subjects with KS and an unexpected HH hormone profile. Methods Magnetic resonance imaging (MRI) of hypothalamus-pituitary region and next generation sequencing (NGS) of congenital HH-associated genes were obtained. A narrative review of the literature was conducted. Results Patients were diagnosed with Klinefelter syndrome following karyotype analysis. Nevertheless, they showed unusual features: both had incomplete puberty, low gonadotropins and testosterone levels, and the first one was anosmic. Sellar lesions were excluded by MRI, and NGS was negative in both subjects. Our data add to those of the only 14 similar cases reported so far. Unexplained HH rarely occurs in KS and is variably associated with anosmia, other pituitary hormones deficiencies and heterogeneous karyotypes. However, most cases show an early, pre-pubertal onset of hypogonadism. If the causes behind this gonadotropins defect are largely unknown, hereby we provide the first review of the literature on this topic and propose some pathogenetic hypotheses, including the coexistence of KS and congenital HH as suggested by overlapping clinical features in some of these patients. Conclusion HH is an exceptional occurrence in Klinefelter syndrome and is associated with heterogeneous phenotypes and, probably, aetiologies. Moreover, KS could underlie HH nonresponsive to gonadotropins. An exhaustive diagnostic workup and a tailored clinical management are advisable in these rare forms.