Brandão Rafael Augusto Castro Santiago, Braga Moises Heleno Vieira, de Souza Atos Alves, Reis Baltazar Leão, Faraj de Lima Franklin Bernardes
Department of Neurosurgery, Santa Casa Hospital, Faculty of Medical Science of Minas Gerais, Belo Horizonte, Brazil.
Surg Neurol Int. 2010 Dec 13;1:79. doi: 10.4103/2152-7806.73802.
Pituicytomas originate from pituicytes, modified glial cells derived from ependymal lineage that are found in the stalk and posterior lobe of pituitary gland. The clinical presentation is similar to other pituitary tumors and imaging exams may suggest pituitary adenoma. The diagnostic is based on histopathological analysis. Surgical treatment can be performed by transsphenoidal approach with good results. The prognostic is good after total tumor resection.
We describe here the case of a 17-year-old patient with a history of persistent headache and visual disturbances. Magnetic resonance imaging demonstrated an enhancing solid sellar mass suggestive of pituitary adenoma. The intrasellar mass was resected through a transsphenoidal approach and the diagnosis of pituicytoma was made after histopathological analysis.
Pituicytomas are rare tumors of the neurohypophysis derived from pituicytes. Their clinical presentation resembles that of non-functional pituitary adenomas, but these two types of tumors are histologically well distinct.
垂体细胞瘤起源于垂体细胞,垂体细胞是源自室管膜谱系的一种经过修饰的神经胶质细胞,存在于垂体柄和垂体后叶。其临床表现与其他垂体肿瘤相似,影像学检查可能提示垂体腺瘤。诊断基于组织病理学分析。可通过经蝶窦入路进行手术治疗,效果良好。肿瘤全切后预后良好。
我们在此描述一名17岁患者,有持续性头痛和视觉障碍病史。磁共振成像显示鞍内有一强化实性肿块,提示垂体腺瘤。经蝶窦入路切除鞍内肿块,组织病理学分析后诊断为垂体细胞瘤。
垂体细胞瘤是源自垂体细胞的神经垂体罕见肿瘤。它们的临床表现与无功能性垂体腺瘤相似,但这两种肿瘤在组织学上有明显差异。