Diabetes and Endocrinology, Queen's Medical Centre Nottingham University Hospital NHS Trust, Nottingham, UK
Pathology, Queen's Medical Centre Nottingham University Hospital NHS Trust, Nottingham, UK.
BMJ Case Rep. 2021 Jan 18;14(1):e239456. doi: 10.1136/bcr-2020-239456.
An 85-year-old man was referred to endocrinology following the discovery of an incidental pituitary mass on cranial imaging which was thought to be a non-functioning adenoma during an admission with headaches, lethargy, confusion and hyponatraemia. He had a history of Hürthle cell carcinoma of the thyroid treated with total thyroidectomy, ablative radioiodine therapy and thyroxine replacement. Subsequently, he developed metastatic spread to the neck, lungs and skeleton. About 9 months later, the patient had deterioration of vision. MRI showed a rapidly expanding pituitary mass with compression of the optic chiasm. Biochemical investigations confirmed hypocortisolism and hypogonadism. The patient underwent trans-sphenoidal resection of the pituitary mass followed by external beam radiotherapy to the pituitary bed. Histopathology confirmed a metastatic deposit of Hürthle cell carcinoma, which is a rare and aggressive variant of follicular thyroid carcinoma.
一位 85 岁男性因头痛、乏力、意识混乱和低钠血症入院时,偶然发现垂体肿块,影像学检查提示为无功能腺瘤,遂被转至内分泌科。该患者曾患有甲状腺 Hurthle 细胞癌,已接受甲状腺全切除术、放射性碘消融治疗和甲状腺素替代治疗。随后,肿瘤转移至颈部、肺部和骨骼。大约 9 个月后,患者出现视力恶化。MRI 显示垂体肿块迅速增大,压迫视交叉。生化检查证实存在皮质醇功能减退和性腺功能减退。患者接受了经蝶窦垂体肿块切除术,随后对垂体床进行了外照射放疗。组织病理学证实了 Hurthle 细胞癌的转移灶,这是滤泡状甲状腺癌的一种罕见且侵袭性变异。