A Case of Hypogonadotropic Hypogonadism in Association with Interhemispheric Lipoma and Hypoplasia of the Corpus Callosum
نویسندگان
چکیده
Isolated hypogonadotropic hypogonadism is characterized by impaired gonadotropin release in the context of normal anatomical and functional anterior pituitary function. The conditions usually responsible for hypogonadotropic hypogonadism are: pituitary adenoma, neoplastic metastasis, granulomatous processes, lymphocitary hypophysitis, histiocytosis X, hemochromatosis, vascular pathologies. We present a case of isolated hypogonadotropic hypogonadism associated with interhemispheric lipoma and hypoplasia of corpus callosum.
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Interhemispheric lipoma: Interval development of an associated cyst
We report a case of an 11-year-old patient who underwent CT imaging for complications of sinusitis, and showed incidental development of an interhemispheric cyst in association with an intracranial lipoma over a 10-year interval. Cysts and lipomas are well described in association with dysgenesis of the corpus callosum. We present an uncommon association, of a new cyst in association with an in...
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Hypogonadotropic hypogonadism (HH) is an uncommon cause of male infertility and a congenital or secondary disorder characterized by delayed or absent sexual maturation. Congenital abnormalities leading to HH are usually the consequence of deficient GnRH secretion occurring either in isolation (idiopathic hypogonadotropic hypogonadism (IHH)), or in association with anosmia (Kallmann syndrome; KS...
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