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一位患有假性甲状旁腺功能减退症所致广泛脑钙化的患者:病例报告。

A patient with extensive cerebral calcification due to pseudohypoparathyroidism: a case report.

机构信息

Sri Jayawardenapura General Hospital, Thalapathpitiya, Nugegoda, Sri Lanka.

出版信息

BMC Endocr Disord. 2019 Dec 19;19(1):142. doi: 10.1186/s12902-019-0475-z.

Abstract

BACKGROUND

Pseudohypoparathyroidism(PHP) is a heterogeneous group of disorders due to impaired activation of c AMP dependant pathways following binding of parathyroid hormone (PTH) to its receptor. In PHP end organ resistance to PTH results in hypocalcaemia, hyperphosphataemia and high PTH levels.

CASE PRESENTATION

A 59 year old male presented with a history of progressive impairment of speech and unsteadiness of gait for 1 week and acute onset altered behavior for 1 day and one episode of generalized seizure. His muscle power was grade four according to MRC (medical research council) scale in all limbs and Chovstek's and Trousseau's signs were positive. Urgent non contrast computed tomography scan of the brain revealed extensive bilateral cerebral and cerebellar calcifications. A markedly low ionized calcium level of 0.5 mmol/l, an elevated phosphate level of 9.5 mg/dl (reference range: 2.7-4.5 mg/dl) and an elevated intact PTH of 76.3 pg/l were noted. His renal functions were normal. His hypocalcemia was accentuated by the presence of hypomagnesaemia. His 25 hydroxy vitamin D level was only marginally low which could not account for severe hypocalcaemia. A diagnosis of pseudohypoparathyroidism without phenotypic defects, was made due to hypocalcaemia and increased parathyroid hormone levels with cerebral calcifications. The patient was treated initially with parenteral calcium which was later converted to oral calcium supplements. His coexisting Vitamin D deficiency was corrected with 1αcholecalciferol escalating doses. His hypomagnesaemia was corrected with magnesium sulphate parenteral infusions initially and later with oral preparations. With treatment there was a significant clinical and biochemical response.

CONCLUSION

Pseudohypoparathyroidism can present for the first time in elderly resulting in extensive cerebral calcifications. Identification and early correction of the deficit will result in both symptomatic and biochemical response.

摘要

背景

假性甲状旁腺功能减退症(PHP)是一组由于甲状旁腺激素(PTH)与其受体结合后,cAMP 依赖途径的激活受损而导致的异质性疾病。在 PHP 中,靶器官对 PTH 的抵抗导致低钙血症、高磷血症和高 PTH 水平。

病例介绍

一名 59 岁男性,因言语渐进性障碍和步态不稳 1 周,急性发作改变行为 1 天,发作 1 次全身性癫痫就诊。他的肌肉力量根据 MRC(医学研究委员会)量表在四肢均为四级,Chovstek 征和 Trousseau 征阳性。脑的非增强 CT 扫描显示广泛的双侧大脑和小脑钙化。明显低的离子钙水平为 0.5mmol/L,升高的磷酸盐水平为 9.5mg/dl(参考范围:2.7-4.5mg/dl),升高的完整 PTH 为 76.3pg/L。他的肾功能正常。低镁血症使他的低钙血症加重。他的 25 羟维生素 D 水平仅略低,不能解释严重的低钙血症。由于低钙血症和甲状旁腺激素水平升高伴大脑钙化,诊断为假性甲状旁腺功能减退症,无表型缺陷。患者最初接受静脉补钙治疗,随后改为口服钙补充剂。他并存的维生素 D 缺乏症用 1α 胆钙化醇递增剂量纠正。他的低镁血症最初用硫酸镁静脉输注,随后用口服制剂纠正。随着治疗,临床和生化反应显著。

结论

假性甲状旁腺功能减退症可首次在老年人中出现,导致广泛的大脑钙化。识别和早期纠正缺陷将导致症状和生化反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c5/6923949/5a63566b8d10/12902_2019_475_Fig1_HTML.jpg

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