Department of Neurosurgery, Brotzu Hospital, Via Peretti 1, 09100 Cagliari, Italy.
J Oncol. 2010;2010:195323. doi: 10.1155/2010/195323. Epub 2010 Jul 8.
Background. Hypophysitis is an inflammatory disease of the pituitary gland that may mimic pituitary tumors clinically and radiologically. Case Description. We report a case of a xanthomatous hypophysitis initially diagnosed as pituitary adenoma. A 31-year-old woman presented with headache, diabetes insipidus, and amenorrhea. A head CT scan showed no intrasellar changes, while an MRI scan showed a sellar cystic mass. An endocrinological work up revealed mild hypocortisolism and diabetes insipidus (DI). Transsphenoidal surgery was performed. The intraoperative histological examination suggested a pituitary adenoma. The removed tissue showed central necrosis surrounded by accumulation of foamy cells and xanthomatous epithelioid cells. The patient made an uneventful postoperative recovery, Nevertheless, DI persisted and the adenohypophysis hypofunction did not recover. Conclusion. We describe an unusual inflammatory lesion of the pituitary gland mimicking an adenoma. A high level of clinical suspicion of inflammatory disorders is necessary for correct diagnosis and optimal management.
垂体炎是一种垂体炎症性疾病,临床上和影像学上可能类似于垂体肿瘤。
我们报告了一例起初被诊断为垂体腺瘤的黄色瘤性垂体炎病例。一名 31 岁女性因头痛、尿崩症和闭经就诊。头颅 CT 扫描未见鞍内改变,而 MRI 扫描显示鞍内囊性肿块。内分泌检查显示轻度皮质醇功能减退和尿崩症(DI)。进行了经蝶窦手术。术中组织学检查提示垂体腺瘤。切除的组织显示中央坏死,周围有泡沫细胞和黄色瘤上皮样细胞堆积。尽管患者术后恢复顺利,但 DI 仍持续存在,腺垂体功能减退未恢复。
我们描述了一种类似腺瘤的垂体炎症性病变,较为罕见。为了正确诊断和优化管理,需要对炎症性疾病保持高度的临床怀疑。