Younes Nidal A, Mahafza Waleed S, Agabi Shukri S
Department of Surgery, Faculty of Medicine, University of Jordan, PO Box 13024, Amman 11942, Jordan.
Saudi Med J. 2004 Nov;25(11):1701-3.
Severe parathyroid bone disease is a rare clinical presentation of primary hyperparathyroidism. Double parathyroid adenomas are even more rare cause of primary hyperparathyroidism. The authors present a case of double parathyroid adenomas in a 48-year-old man, who presented with painful left lower limb swelling, which was slowly growing in size in the last 20 years. Magnetic resonance imaging revealed a cystic bony lesion and coincidentally, a urinary bladder calculus. Biopsy of the mass revealed giant cell lesion. Laboratory investigations showed hypercalcemia and hypophosphatemia with elevated parathyroid hormone level. A computerized tomography scan of the neck delineated an adenoma of the left superior parathyroid gland, which was surgically removed. The left inferior parathyroid was also enlarged and was removed. Histological diagnosis confirmed double parathyroid adenomas. The rarity and the interesting clinical presentation of such association are discussed.
严重甲状旁腺骨病是原发性甲状旁腺功能亢进症的一种罕见临床表现。双发性甲状旁腺腺瘤更是原发性甲状旁腺功能亢进症的罕见病因。作者报告了一例48岁男性双发性甲状旁腺腺瘤病例,该患者表现为左下肢疼痛性肿胀,在过去20年中肿胀大小逐渐增大。磁共振成像显示有一个囊性骨病变,巧合的是,还有一个膀胱结石。肿块活检显示为巨细胞病变。实验室检查显示高钙血症、低磷血症以及甲状旁腺激素水平升高。颈部计算机断层扫描显示左上方甲状旁腺有一个腺瘤,已通过手术切除。左下方甲状旁腺也肿大并被切除。组织学诊断证实为双发性甲状旁腺腺瘤。本文讨论了这种关联的罕见性及其有趣的临床表现。