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A variety of lesions can invade and destroy all or a large part of the hypothalamus. These include sarcoid and other granulomatous diseases, an idiopathic in ammatory disease, and germ-cell and other tumors. The hypothalamus is involved in approximately 5 percent of cases of sarcoidosis, sometimes as the primary manifestation of the disease, but more often in combination with facial palsy and hilar lymphadenopathy. An elevation of angiotensin-converting factor, particularly in the cerebrospinal uid (CSF), con rms the diagnosis. The lesions are visible by magnetic resonance imaging (MRI) (see Fig. 32-2). Tumors that involve the hypothalamopituitary axis include metastatic carcinoma, lymphoma, craniopharyngioma, and a variety of germ-cell tumors. The latter (reviewed by Jennings et al) include germinomas, teratomas, embryonal carcinoma, and choriocarcinoma. They develop during childhood, tend to invade the posterior hypothalamus, and are accompanied in some instances by an increase in serum alpha fetoprotein or the beta subunit of chorionic gonadotropin. A unique syndrome of gelastic epilepsy is caused by a hamartoma of the hypothalamus (see Chap. 16). Among the in ammatory conditions, infundibuloneurohypophysitis, or infundibulitis, is a cryptogenic in ammation of the neurohypophysis and pituitary stalk, with thickening of these parts by in ltrates of lymphocytes (mainly T cells) and plasma cells (Imura et al). It is thought to be an autoimmune disorder. Histiocytosis X a group of diseases comprising Letterer-Siwe disease, HandSchuller-Christian disease, and eosinophilic granuloma impli cates multiple organs, including the hypothalamus and neighboring structures and leptomeninges (often causing cells to appear in the CSF). These conditions of children pursue an indolent course. The cell type is a proliferating histiocyte. ssrs gs1 128 SSRS GS1-128 / EAN-128 Generator - OnBarcode
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