Searchable abstracts of presentations at key conferences in endocrinology

ea0063p707 | Pituitary and Neuroendocrinology 2 | ECE2019

A case of isolated adrenocorticotropic hormone deficiency diagnosed with ventricular fibrillation by prolonged QT interval

Ebashi Chihiro , Huzita Syohei , Hishida Ai , Tobita Satoshi , Hosogi Shingo , Yamamoto Katsuhito , Matsuoka Toshiki , Sugano Hisashi

Introduction: Isolated adrenocorticotropic hormone (ACTH) deficiency (IAD) is a rare disease, which is characterized by secondary adrenal insufficiency with low cortisol production, and normal secretion of pituitary hormones other than ACTH. Although it is known that QT prolongation is sometimes observed in patients with IAD, reports on IAD in which the QT interval was sufficiently prolonged to cause Torsades de Pointes (TdP) are rare. We described the case of a patient with I...

ea0063p710 | Pituitary and Neuroendocrinology 2 | ECE2019

Lymphocytic hypophysitis with disturbance of both anterior and posterior pituitary function preceded by headache, diagnosed as meningitis

Hishida Ai , Ebashi Chihiro , Ikeda Tatsuya , Yano Hiroko , Sawada Tsutomu , Fukuda Maki , Hata Yasuhiro , Sugano Hisashi

Introduction: Lymphocytic hypophysitis (LH) is a heterogeneous inflammatory condition in the pituitary gland, which may cause hormonal deficiency. However, some patients with LH initially present with headache.Case: A 63-year-old woman complained of a severe headache for 1 month. Examination of cerebrospinal fluid (CSF) showed increased lymphocyte counts, indicating meningitis. Contrast-enhanced magnetic resonance imaging (MRI) revealed an expanding sell...