ISPUB.COM The Internet Journal of Endocrinology Volume 5 Number 1 1 of 4 Primary empty sella: an unusual presentation A Sofi, M Kamili, S Rashid, M Khujwal, A Khaliq Citation A Sofi, M Kamili, S Rashid, M Khujwal, A Khaliq. Primary empty sella: an unusual presentation. The Internet Journal of Endocrinology. 2008 Volume 5 Number 1. Abstract Empty sella although reported to occur in 5.5% of the population,1 uncommonly presents with endocrine abnormalities. When they do present, endocrine disturbances are usually mild and usually represent a small increase in prolactin levels in adults. We present here an unusual case who presented clinically with primary amenorrhea where the cause remained undiagnosed for more than a decade by which time she had progressed to panhypopituitarism. CASE HISTORY A 25 year old female presented to the outpatient department of internal medicine with a previous diagnosis of primary amenorrhea and now increasing fatigue and lack of energy for the past year. She had also felt sleepier than before over this same period and would nap several times a day. She had been investigated previously for her primary amenorrhea at the age of 18 years. However, an incomplete hormonal profile done due to lack of available healthcare resources had revealed nothing abnormal. By the time she came to us she seemed resigned to her diagnosis of primary amenorrhea of unknown cause and appeared more concerned with her fatigue. She denied fever, cough, change in bowel habits, blood with stools, rash, jaundice, joint pains or swelling, snoring, headache, visual disturbances, or any nipple discharge. Her past history other than her amenorrhea was unremarkable. There was no family history of a similar illness. She was not on any medications. On physical examination she was slightly built. Her pulse was 62/min and regular in rhythm. Her blood pressure was 80/60 mm Hg. Her secondary sexual characters appeared normal. She had no visual field deficits. The examination of her fundus failed to reveal any abnormalities. The rest of her systemic examination was also unremarkable. Her blood counts and biochemical profile was normal. An x- ray chest showed no abnormalities. An ultrasound of the abdomen revealed a normal uterus and ovaries. DISCUSSION Considering her previous history of primary amenorrhea, present symptoms suggestive of probable hypothyroidism and a low resting blood pressure, we thought primarily in terms of pituitary hypofunction secondary to a slow growing non functioning pituitary adenoma. A pituitary adenoma causing no signs of compression of the surrounding structures, however, seemed odd. Another possibility seemed pituitary dysfunction limited to gonadotropin secretion with coincident adrenal loss of function. A low accompanying blood pressure also made a probable primary adrenal disturbance likely. With theses possibilities in mind, we next proceeded to resolve our doubts by determining the patient's LH and FSH levels, thyroid function, prolactin levels and morning cortisol levels. Her profile was revealing; both FSH and LH were very low, 7.4 U/L and 2.4 U/L respectively. FT3 & FT4 were undetectable, while TSH (4.8 mU/L) although within normal range was inappropriately low for the FT3 and FT4 levels. Cortisol was low normal at 12.8 µg/dL (12-25 µg/dL) and prolactin was mildly elevated at 29.4 ng/mL. This pointed to our first suspicion of hypopituitarism and it remained to be determined how extensive it was and what was its underlying cause. So far, our hypothesis of an underlying pituitary adenoma seemed justified; especially with elevated prolactin levels pointing towards stalk compression. However, accompanying hypothyroidism could also account for the rise in prolactin levels. On the other hand, the lack of clinical signs of compression of surrounding structures and absence of evidence of a raised intracranial pressure put the presence of an adenoma large enough to cause extensive pituitary hormonal deficiency in doubt. We decided, therefore, to first maintain our pursuit of determining the extent and level of pituitary hypofunction. This we completed by stressing the patient with insulin induced hypoglycemia and measuring