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Brown tumor involving the sellar-parasellar region mimicking pituitary adenoma as the tip of the iceberg of generalized primary hyperparathyroidism

机译:涉及鞍状-鞍旁区域的褐色肿瘤模仿垂体腺瘤作为广泛性原发性甲状旁腺功能亢进的冰山一角

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摘要

The authors present a case study of a 40-year-old man with advanced, previously undiagnosed primary hyperparathyroidism (PHPT), which first manifestation directing to correct diagnosis was sellar-parasellar brown tumor. Further studies disclosed PHPT. The patient presented many of the classic signs of the disease, including renal stones, duodenal ulcer, muscle weakness and bone pains, but suspicion of PHPT was made on the base of a postoperative histological examination of the sellar- parasellar tumor. Laboratory investigations showed hypercalcaemia, hypophosphataemia, elevated levels of parathyroid hormone and alkaline phosphatase. A skeletal survey showed generalized decreased density of bones and multiple brown tumors. The problems of diagnosis and localization of parathyroid glands have been discussed. The literature has been reviewed and the importance of early diagnosis and treatment has been stressed.
机译:作者介绍了一个病例,该病例研究了一个40岁,先前未被诊断的晚期原发性甲状旁腺功能亢进症(PHPT)的男子,该病的首个指导正确诊断的是蝶鞍-鞍旁棕色肿瘤。进一步的研究揭示了PHPT。该患者表现出该病的许多典型体征,包括肾结石,十二指肠溃疡,肌肉无力和骨痛,但怀疑PHPT是基于术后鞍旁肿瘤的组织学检查。实验室检查显示高钙血症,低磷酸血症,甲状旁腺激素和碱性磷酸酶水平升高。骨骼检查显示骨骼密度普遍降低,并出现多个棕色肿瘤。讨论了甲状旁腺的诊断和定位问题。已经审查了文献,并强调了早期诊断和治疗的重要性。

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