Khalil A, Kovacs K, Sima A A, Burrow G N, Horvath E
J Endocrinol Invest. 1984 Aug;7(4):399-404. doi: 10.1007/BF03351025.
A 32-year-old woman with persistent postpartum galactorrhea, hyperprolactinemia and a sellar configuration compatible with pituitary adenoma underwent transsphenoidal surgery. Mild hyperthyroidism had been suspected clinically preoperatively and thyroxine plus cortisol therapy was given. Morphological features of pituitary thyrotroph hyperplasia were present as shown by light microscopy, immunoperoxidase staining and electron microscopy. The thyrotroph hyperplasia was secondary to primary hypothyroidism as demonstrated by the TSH response to TRH stimulation and subsequent suppression with thyroid hormone treatment. Although prolonged severe hypothyroidism has been reported to cause pituitary enlargement, this is the first case of thyrotroph hyperplasia with detailed morphologic study of the surgically-removed adenohypophysial tissue. The presentation of this patient calls attention to the possibility of mistaking pituitary enlargement due to primary hypothyroidism for a prolactinoma.
一名32岁女性,患有持续性产后溢乳、高泌乳素血症,蝶鞍形态符合垂体腺瘤,接受了经蝶窦手术。术前临床曾怀疑有轻度甲状腺功能亢进,并给予了甲状腺素加皮质醇治疗。光镜、免疫过氧化物酶染色及电镜检查显示存在垂体促甲状腺细胞增生的形态学特征。促甲状腺细胞增生继发于原发性甲状腺功能减退,这可通过促甲状腺激素对促甲状腺激素释放激素刺激的反应以及随后甲状腺激素治疗后的抑制作用得到证实。尽管有报道称长期严重甲状腺功能减退会导致垂体增大,但这是首例对手术切除的腺垂体组织进行详细形态学研究的促甲状腺细胞增生病例。该患者的表现提醒人们注意,原发性甲状腺功能减退所致垂体增大可能被误诊为泌乳素瘤。