Mautalen C A, Kvicala R, Perriard D, Bugnard E, Rossi E, Duhart J
Am J Med Sci. 1978 Nov-Dec;276(3):363-8. doi: 10.1097/00000441-197811000-00015.
A patient in whom hypoparathyroidism developed as a complication of posttransfusional iron storage disease is described. The hypoparathyroidism occurred after more than 15 years of receiving blood transfusions at frequent intervals. In this patient with thalassemia major the serum PTH levels were undetectable. 25-hydroxy-vitamin D3 corrected the hypocalcemia that was resistant to vitamin D2, probably due to the associated liver dysfunction. Other cases reported in the literature are reviewed. It is suggested that hypoparathyroidism occurs more frequently than usually suspected in patients with iron storage disease.
本文描述了一名患者,其甲状旁腺功能减退作为输血后铁储存疾病的并发症出现。甲状旁腺功能减退在频繁输血超过15年后发生。在这名重型地中海贫血患者中,血清甲状旁腺激素水平检测不到。25-羟维生素D3纠正了对维生素D2耐药的低钙血症,这可能归因于相关的肝功能障碍。文中还回顾了文献中报道的其他病例。提示甲状旁腺功能减退在铁储存疾病患者中的发生率比通常怀疑的更高。