WebLymphocytic hypophysitis (LH), also known as autoimmune hypophysitis, is characterized by diffuse lymphocyte (CD4+ T-cell predominant) infiltration of the pituitary gland with a 9:1 female to male predominance, most commonly occurring during the third trimester of pregnancy or the early postpartum period. WebMay 1, 1994 · Jensen MD, Handwerger BS, Scheithauer BW, Carpenter PC, Mirakian R, Banks PM. Lymphocytic hypophysitis with isolated corticotropin deficiency. Ann Intern Med. …
Frontiers A Remarkable Response of Granulomatous Hypophysitis …
WebJul 1, 1991 · J Clin Endocrinol Metab 1987;64:631-4. 6. Jensen MD, Handwerger BS, Scheithauer BW, Carpenter PC, Mirakian R, Banks PM. Lymphocytic hypophysitis with isolated corticotropin deficiency. Ann Intern Med 1986;105:200-3. ... Lymphocytic hypophysitis with isolated corticotropin deficiency. Ann Intern Med, 105 (1986), pp. 200 … WebFeb 1, 1998 · Cytosolic Autoantigens in Lymphocytic Hypophysitis1 The Journal of Clinical Endocrinology & Metabolism Oxford Academic Lymphocytic hypophysitis was first recognized postmortem, then by biopsy, but detection of antipituitary autoantibodies by immunofluorescence has proved unsatis health horizons abq
MECHANISMS IN ENDOCRINOLOGY: Hypophysitis: diagnosis and treatment - eje
WebLymphocytic infundibulohypophysitis is an inflammatory condition affecting the posterior pituitary gland and often presenting clinically with cranial diabetes insipidus. 1 It is distinct from lymphocytic hypophysitis, which affects the anterior pituitary and usually presents at the end of pregnancy with visual disturbances. 2 Differentiating … WebApr 2, 2014 · We report a male patient who presented with severe fasting hypoglycemia in which extensive pituitary and adrenal investigations were diagnostic of isolated ACTH deficiency of pituitary origin. The finding of autoimmune subclinical primary hypothyroidism strongly suggested an autoimmune etiology of the pituitary disease. WebDec 17, 2024 · Immune-mediated hypophysitis is often unrecognized and can range from isolated pituitary hormone deficiency to, rarely, panhypopituitarism. Severe cases can cause pituitary gland enlargement that can result in visual disturbances due to compression on the optic chiasm, and potentially death from adrenal crisis. health hope and healing