Al-Herbish A S, Bailey J D, Kooh S W
Department of Pediatrics (39), College of Medicine, King Saud University, PO Box 90533, Riyadh 11623.
Saudi Med J. 2000 Aug;21(8):765-8.
This is a case report of 2 patients who were diagnosed to have autoimmune polyglandular disease type 1. Both developed mucocutaneous candidiasis, hypoparathyroidism, vitiligo, and adrenocortical insufficiency. Both were noticed to have subnormal linear growth velocity and delayed bone age. Both showed subnormal stimulated serum growth hormone values indicating growth hormone deficiency. The first case showed favorable response to growth hormone therapy.
这是一篇关于2例被诊断为1型自身免疫性多腺体疾病患者的病例报告。两名患者均出现皮肤黏膜念珠菌病、甲状旁腺功能减退、白癜风和肾上腺皮质功能不全。两人均被发现线性生长速度低于正常水平且骨龄延迟。两人的血清生长激素刺激值均低于正常水平，提示生长激素缺乏。首例患者对生长激素治疗反应良好。
