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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Bestepe N, Aydin C, Tam AA, Ercan K, Ersoy R, Cakir B
Empty Sella in a Patient with Clinical and Biochemical Diagnosis of Acromegaly
Acta Endo (Buc) 2022, 18 (1): 97-101doi: 10.4183/aeb.2022.97
Background. Acromegaly is an acquired disorder
related to excessive production of growth hormone (GH)
and insulin-like growth factor-1 (IGF-1). Empty sella (ES)
is an anatomical condition of sella turcica that is partially
or completely filled with cerebrospinal fluid mainly due
to intrasellar herniation of subarachnoid space. Here,
we describe a patient who presented with clinical and
biochemical features of acromegaly and who had an ES on
pituitary magnetic resonance imaging (MRI).
Case report. A 73-year-old male patient was
consulted in our clinic because of the acromegalic phenotype
while planning for colorectal adenocarcinoma surgery. The
patient noticed gradual enlarging of his hands, feet and nose for
30 years, but never consulted to any clinician for this reason.
Serum GH was 20.6 ng/mL (normal <3 ng/mL) and IGF-1 was
531 ng/mL (normal, 69–200 ng/ml). An oral glucose tolerance
test showed no suppression of GH values. T1-weighted MRI
revealed an ES. 18F-FDG PET/CT and Ga-DOTATADE
PET/CT did not show any finding consistent with ectopic GH
secretion. Growth hormone releasing hormone (GHRH) was
within the normal range (<100mg/dL). He was treated with
long-acting octreotide 20 mg per 28 days. At the 6th month of
treatment, serum GH and IGF-1 levels were decreased to 5.45
ng/mL and 274 ng/mL, respectively.
Conclusion. The mechanism underlying the
association of acromegaly and ES remains unclear. Apoplexy
on existing pituitary adenoma and then formation of necrosis
can proceed to ES. Since our patient did not have a history
of pituitary apoplexy and we could not find any reason for
secondary ES, we considered primary ES.
Keywords: acromegaly, empty sella syndrome,
pituitary tumor.
Correspondence: Nagihan Bestepe MD, Ankara City Hospital, Dept. of Endocrinology and Metabolism, Ankara, Turkey, E-mail:
nagihanbestepe@gmail.com