Pituitary adenoma occurring with acromegaly coexisting with partially empty sella syndrome Case report
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Abstract
Pituitary microadenoma occurring with acromegaly coexisting with empty sella syndrome is a rare clinical case. The main symptoms result from the presence of hormonally active pituitary tumor. Empty sella syndrome may hinder correct and prompt diagnosis, which may be important for effective therapy. We present a case of a 67-year-old woman admitted to hospital with acromegaly. MRI of the pituitary revealed partially empty sella and pituitary microadenoma. The patient underwent surgery. Follow-up MRI revealed regression of the pituitary adenoma without signs of recurrence during observation. We also present a review of literature.
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Copyright: © Medical Education sp. z o.o. This is an Open Access article distributed under the terms of the Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). License (https://creativecommons.org/licenses/by-nc/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Address reprint requests to: Medical Education, Marcin Kuźma (marcin.kuzma@mededu.pl)
References
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