VOLUME 5 , ISSUE 1 ( January-June, 2017 ) > List of Articles
Raju PV, Jagadeesan M, Halleys Kumar, Magesh Kumar S, Hemachandrika C
Keywords : empty sella, Empty Sella Syndrome, hypopituitarism, pituitary dysfunction
Citation Information : PV R, M J, Kumar H, S MK, C H. Empty Sella Syndrome: A case report. 2017; 5 (1):46-48.
DOI: 10.5005/NJP-11056-05_01_09
License: CC BY-NC 4.0
Published Online: 01-06-2017
Copyright Statement: Copyright © 2017; NA
A 55 year old female patient presented with history of giddiness and fatigue of one year duration. She had pallor, diffuse hyperpigmentation of skin and mucosal surfaces, low blood pressure (90/60 mm Hg), hypoglycemia, hyponatremia (118 mEq/L), hypokalemia (2.7 mEq/L) and elevated serum ACTH levels (21 pmol/L) suggestive of hypocortisolism. On imaging, MRI Brain showed features suggestive of an empty sella. In the absence of any other inciting factors, a diagnosis of Primary Empty Sella (PES) syndrome was made. The patient was treated with levothyroxine, steroids, hypertonic saline and potassium supplements following which she recovered rapidly. An empty sella occurs due to herniation of the arachnoid membrane through an incompetent diaphragma sellae. Primary empty sella syndrome is considered as a less common entity and is usually asymptomatic and can be an incidental finding.