Focal Seizures in a Patient With Chronic Basal Ganglia Calcifications Secondary to Idiopathic Primary Hypoparathyroidism.

JCEM case reports Pub Date : 2024-05-21 eCollection Date: 2024-05-01 DOI:10.1210/jcemcr/luae093
Jennifer Zhang, Karen Van, Patrick Carney, Christopher Gilfillan, Mathis Grossmann
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Abstract

Patients with hypoparathyroidism can present with concurrent basal ganglia calcifications (BGCs). The exact pathogenesis is unknown, although it is thought to relate to calcium-phosphate deposition from chronic hypocalcemia and hyperphosphatemia. We present the case of a 65-year-old man with known idiopathic primary hypoparathyroidism and concurrent extensive BGC. Thirty years after diagnosis, he presented with focal seizures despite a decade of stable intracranial calcifications on imaging. Serum calcium, phosphate, 25-hydroxyvitamin D, and parathyroid hormone levels were well controlled during this period. He was commenced on lifelong levetiracetam with subsequent seizure remission. Given the scarcity of literature surrounding focal seizures and BGC, it is essential to raise awareness in this area.

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特发性原发性甲状旁腺功能减退症继发慢性基底节钙化患者的局灶性癫痫发作
甲状旁腺功能减退症患者可并发基底节钙化(BGCs)。确切的发病机制尚不清楚,但有人认为这与慢性低钙血症和高磷血症导致的钙磷酸盐沉积有关。我们介绍了一名65岁男性的病例,他患有已知的特发性原发性甲状旁腺功能减退症,并同时患有广泛的BGC。确诊30年后,他出现了局灶性癫痫发作,尽管影像学检查显示他的颅内钙化已经稳定了10年。在此期间,血清钙、磷酸盐、25-羟维生素D和甲状旁腺激素水平控制良好。他开始终身服用左乙拉西坦,随后癫痫发作得到缓解。鉴于有关局灶性癫痫发作和 BGC 的文献很少,因此必须提高人们对这一领域的认识。
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