Ariella Maisie Sugiarto, - and Soebagijo Adi Soelistijo, Soebagijo A female with isolated hypogonadotropic hypogonadism: A case report and review article. Annals of Medicine and Surgery, 74. ISSN 2049-0801

	Text (Artikel) 22. Artikel.pdf Download (3MB)
	Text (Kualitas Karil & Kesesuaian Bidang Ilmu) 22 karil.pdf Download (115kB)
	Text (Turnitin) 22. turnitin.pdf Download (2MB)
	Text 22. korespondensi.pdf Download (298kB)
	Text (Bukti Korespondensi) 22. korespondensi.pdf Download (298kB)

Abstract

Abstract Background: Isolated Hypogonadotropic Hypogonadism (IHH) is a clinical syndrome that results from gonadal failure due to abnormal pituitary gonadotropin levels, in the presence of normal baseline and reserve testing of the remaining pituitary hormones. Case presentation: An 18 years old female came with primary amenorrhea, accompanied by poor breast and pubic development, with low levels of estradiol and gonadotropins but normal levels of other anterior pituitary hormones. Imaging of the hypothalamic-pituitary region revealed hypophyseal hypoplasia due to ischemia. Sex steroids therapy was given to induce pubertal development. IHH represents a rare condition but with a good prognosis. Discussion: Early diagnosis and treatment can prevent negative physical and psychological sequelae, and restore fertility in affected patients. Constant surveillance is required due to the possibility of gonadal axis reversal and/or relapse of gonadal axis failure and to identify any adverse effects related to therapy. Conclusion: Early identification of IHH can help in treatment efficiency.

Actions (login required)

View Item