Searchable abstracts of presentations at key conferences in endocrinology

ea0065p319 | Neuroendocrinology | SFEBES2019

Panhypopituitarism secondary to hypothalamic involvement in Isolated Langerhans cell Histiocytosis

Khan Huma Humayun , Humayun Asif

A 68-year-old male presented with fatigue and acute onset polyuria and polydipsia. There was no history of headaches, visual symptoms, previous cranial radiations, chemotherapy or CNS infections. Investigations revealed normal fasting glucose, urea, creatinine, liver functions and electrolytes including calcium. Further workup including pituitary profile, paired osmolalities and water deprivation test confirmed hypopituitarism and cranial diabetes insipidus (Table 1). The unde...

ea0048wa8 | Workshop A: Disorders of the hypothalamus and pituitary | SFEEU2017

Aggressive prolactinoma

Butt Nouman , Haider Najaf , Malik Asif Humayun , Al-Mrayat Ma'en

A 50 year old male presented with left visual field loss, afferent pupillary defect and reduced libido in 1999. Initial pituitary profile showed prolactin 130 000 mu/l (55.4–276), and testosterone was 5 nmol/l (10–27.6). MRI pituitary showed giant pituitary macroadenoma compressing chiasm. He was started on Cabergoline with subsequent improvement in visual fields, prolactin levels and size of adenoma on subsequent MRI. His disease remained stable on ...