| Literature DB >> 31949764 |
Min He1, Niandong Zheng2, Jing Zhang3, Zhihong Hu4, Guoliang You4, Qingqing Ren3, Hao Liu3, Jianguo Xu3.
Abstract
A gangliocytoma in the sellar region is extremely rare. We report a rare case of mixed gangliocytoma and growth hormone (GH)-secreting adenoma in a 50-year-old woman, who presented with acromegaly. Laboratory investigations revealed high levels of GH and insulinlike growth factor 1 (IGF-1). Sellar computed tomography scan and contrast enhanced magnetic resonance imaging (CE-MRI) showed a sellar mass. Based on clinical, biochemical, and radiologic evaluations, GH-secreting adenoma was diagnosed and operated by endonasal transsphenoidal approach achieving total removal of the tumor. After surgery, histopathological examination demonstrated mixed gangliocytoma and GH-secreting adenoma in the resected lesion. The clinical, radiological, and operative data are reviewed, as are the histological findings. To our knowledge, few cases of mixed gangliocytoma and GH-secreting adenoma have been reported. IJCEPEntities:
Keywords: Pituitary adenoma; gangliocytoma; growth hormone
Year: 2018 PMID: 31949764 PMCID: PMC6962879
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625