Simşek Enver, Simşek Tülay, Savaş-Erdeve Senay, Erdoğmuş Beşir, Döşoğlu Murat
Department of Pediatrics, Düzce University Faculty of Medicine, Düzce, Turkey.
Turk J Pediatr. 2009 Nov-Dec;51(6):624-30.
We report two cases with primary autoimmune hypothyroidism and an ectopic thyroid gland causing pituitary enlargement mimicking pituitary macroadenoma. One of the cases presented with complaints of headache and short stature and the other case with a complaint of menorrhagia. In both cases, the pituitary mass and symptoms resolved with levothyroxine replacement. Normal menses resumed. However, pituitary dynamic tests revealed persistent growth hormone and gonadotropin deficiency in one case and growth hormone deficiency in the other. To our knowledge, this is the first report in an adolescent of hypogonadotropic hypogonadism, growth hormone deficiency, and menorrhagia associated with pituitary hyperplasia secondary to primary hypothyroidism. The recognition of the association between reversible pituitary hyperplasia and primary hypothyroidism might eliminate unnecessary surgery.
我们报告了两例原发性自身免疫性甲状腺功能减退症合并异位甲状腺导致垂体增大、酷似垂体大腺瘤的病例。其中一例表现为头痛和身材矮小,另一例表现为月经过多。在这两例中,垂体肿块和症状在左甲状腺素替代治疗后均得到缓解。月经恢复正常。然而,垂体动态试验显示,其中一例持续存在生长激素和促性腺激素缺乏,另一例存在生长激素缺乏。据我们所知,这是青少年中首例关于原发性甲状腺功能减退继发垂体增生相关的低促性腺激素性性腺功能减退、生长激素缺乏和月经过多的报告。认识到可逆性垂体增生与原发性甲状腺功能减退之间的关联可能避免不必要的手术。