A Rare Case of Pituicytoma Presenting Cystic Formation
- Authors
- Ha, Young Soo; Lee, Soo Eon; Park, Sung Choon; Ahn, Sung Yeol; JUNG, YOON YANG
- Issue Date
- Oct-2021
- Publisher
- 대한뇌종양학회
- Keywords
- Brain neoplasm; Cyst; Immunohistochemistry
- Citation
- Brain Tumor Research and Treatment, v.9, no.2, pp 70 - 74
- Pages
- 5
- Indexed
- KCI
- Journal Title
- Brain Tumor Research and Treatment
- Volume
- 9
- Number
- 2
- Start Page
- 70
- End Page
- 74
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/140645
- DOI
- 10.14791/btrt.2021.9.e11
- ISSN
- 2288-2405
2288-2413
- Abstract
- Pituicytoma is a rare solid benign tumor of the sellar and/or suprasellar region originating from the pituicytes of the neurohypophysis or infundibulum, which is not differentiated from a pituitary adenoma that is diagnosed mostly in the sellar and/or suprasellar region. In addition, cystic tumors are very rare and have not been reported due to their solid and hypervascular natures. A 33-year-old man presented with a chronic headache which exacerbated recently. MRI was performed and revealed a cystic tumor in the sellar and suprasellar regions with a small parenchymal island in the cyst compressing the optic chiasm. The endoscopic endonasal transsphenoidal approach was used to remove the tumor. Immunohistochemical staining was positive for thyroid transcription factor 1, S-100 protein, and glial fibrillary acidic protein. The pituicytoma was diagnosed based on histologic findings. The authors review herein the literature on clinical presentation, diagnosis, surgical management, and outcome.
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