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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)
Korkmaz H, Akarsu E, Özkaya M, Öztürk ZA, Tutar E, Araz M
Plurihormonal Pituitary Adenoma: Acromegaly Associated with Subclinical Cushing’s Disease
Acta Endo (Buc) 2015, 11 (3): 389-393doi: 10.4183/aeb.2015.389
A 52-year old women was diagnosed with
acromegaly 5 years ago, and transseptal transsphenoidal
pituitary microsurgery has been performed. Later the patient
did not come to controls and the complaints prior to operation
growth of the hands and feet, headache, sweating and resistant
hypertension have continued. She was referred to our clinic
with the same complaints. Physical examination showed
typical acromegalic features without typical Cushingoid
features. Magnetic resonance imaging of the brain revealed
the presence of a pituitary macroadenoma. Basal plasma levels
of growth hormone (GH) and insulin-like growth factor-1
(IGF-1) levels were high. GH suppression was not observed
in 75 gr oral glucose suppression test. Due to refractory
hypertension and central obesity hypothalamo-pituitaryadrenal
(HPA) axis was evaluated. HPA showed a lack of
circadian rhythm of adrenocorticotropic hormone (ACTH)
and cortisol, non-suppressibility to 1 mg overnight and
classical 2 day low-dose dexamethasone, but suppressibility
to high-dose (8 mg) dexamethasone. The tumour resected by
transsphenodial surgery was histopathologically consistent
with the diagnosis of adenoma. Immunostaining showed GH
and ACTH producing cells. After surgery plasma GH and
IGF-1 levels decreased to normal along with normalization
of HPA axis. Hypertension disappeared without medical
treatment after removal of the pituitary tumour. This is a
very rare case of GH-producing pituitary adenoma causing
typical acromegaly with concomitant production of ACTH
causing subclinical Cushing’s disease.
Keywords: Acromegaly, subclinical Cushing’s disease, plurihormonal pituitary adenoma.
Correspondence: Hakan Korkmaz MD, Gaziantep University, Faculty of Medicine, Department of Internal Medicine, Division of Endocrinology, 27100 Sahinbey, Gaziantep, Turkey, E-mail: drhkorkmaz@yahoo.com.tr