Pituitary Macroadenoma Manifesting As Acromegaly: A Case Report

Background: Acromegaly is an uncommon clinical disorder driven by high serum levels of growth hormone (GH) and insulin-like factor 1 (IGF-1). Over 99% patients with acromegaly harbor a GH emitting pituitary adenoma. Pituitary tumors represent about 15% essential intracranial neoplasms. Case presentation: A 38 years old woman, was referred to the H. Adam Malik central public hospital on December 15th, 2020, chief complaints enlarged fingers toes. The patient complained that patient's toes were getting bigger in past 2 years. brain MRI performed showed intrasella spherical intensity lesions measuring ± 2.3x1.5x2 cm impression macroadenoma. later diagnosed due Therefore treated administration sandostatin injection, novorapid 6-6-6 IU SC, then 0-0-12 3x1 salt capsules. also consulted neurosurgery department for surgical management plans Ophthalmology Department. Conclusion: We report instance suspected because macroadenoma unmistakable highlights, comprehensive management.