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[纹状体苍白球齿状核钙化、甲状旁腺功能减退与神经学特征:一项病例系列研究]

[Striatopallidodentate calcinosis, hypoparathyroidism and neurological features: a case series study].

作者信息

El Otmani H, Lahlou I, Raji L, Omari S, Belmansour Y, Moutaouakil F, Boulaajaj F-Z, Mouden M, Gam I, Hakim K, El Moutawakil B, Rafai M-A, Fadel H, Slassi I

机构信息

Service de neurologie, CHU d'Ibn Rochd, 1, rue des Hôpitaux, Casablanca, Maroc.

出版信息

Rev Neurol (Paris). 2013 Jun-Jul;169(6-7):495-501. doi: 10.1016/j.neurol.2012.11.005. Epub 2013 Mar 21.

Abstract

INTRODUCTION

The respective roles of hypocalcemia and intracerebral calcifications in the occurrence of various neurological manifestations in hypoparathyroidism is not entirely clear. Nevertheless, therapeutic and prognostic implications are important.

OBJECTIVES

We analyze the neurological clinical aspects observed in hypoparathyroidism and correlate them to the biological calcium abnormality and radiological CT scan findings. We also compare these results with data reported in the idiopathic form of striatopallidodentate calcinosis.

PATIENTS

The neurological clinical, CT scan findings and outcome have been retrospectively studied in patients recruited during 13 years (2000-2012) for neurological features associated with hypoparathyroidism or pseudohypoparathyroidism.

RESULTS

Twelve patients with primary hypoparathyroidism (n=5), secondary to thyroidectomy (n=4) and pseudohypoparathyroidism (n=3) were studied. The sex-ratio was 1 and mean age was 39 years. All patients had a tetany, 60% had epilepsy, associated in one patient with "benign" intracranial hypertension; 50% had behavioral changes. Response to calcium therapy was excellent for all these events. Moderate cognitive deficit was noted in three patients (25%), parkinsonism in two patients and hyperkinetic movement disorders in one other. These events were not responsive to calcium therapy and were more common in cases of extensive brain calcifications and in patients who had pseudohypoparathroidism.

COMMENTS

This study suggests that, in patients with hypoparathyroidism, epilepsy and psychiatric disorders are induced by hypocalcemia and reversible after its correction. Cognitive and extrapyramidal impairment seem to be related to the progressive extension of intracerebral calcification, particularly in patients with a late diagnosis. In patients with pseudohypoparathyroidism, this finding is different because of the contribution of other factors, specific to this disease.

摘要

引言

低钙血症和脑内钙化在甲状旁腺功能减退症各种神经表现发生中的各自作用尚不完全清楚。然而,其治疗和预后意义很重要。

目的

我们分析甲状旁腺功能减退症患者的神经临床方面,并将其与生物钙异常及放射学CT扫描结果相关联。我们还将这些结果与特发性纹状体苍白球齿状核钙化症报道的数据进行比较。

患者

对在13年(2000 - 2012年)期间因与甲状旁腺功能减退症或假性甲状旁腺功能减退症相关的神经特征而招募的患者进行了神经临床、CT扫描结果及预后的回顾性研究。

结果

研究了12例原发性甲状旁腺功能减退症患者(n = 5)、甲状腺切除术后继发性甲状旁腺功能减退症患者(n = 4)和假性甲状旁腺功能减退症患者(n = 3)。男女比例为1,平均年龄为39岁。所有患者均有手足搐搦,60%有癫痫发作,其中1例伴有“良性”颅内高压;50%有行为改变。所有这些症状对钙剂治疗反应良好。3例患者(25%)有中度认知缺陷,2例有帕金森综合征,1例有运动增多性运动障碍。这些症状对钙剂治疗无反应,在广泛脑钙化的病例及假性甲状旁腺功能减退症患者中更常见。

评论

本研究表明,在甲状旁腺功能减退症患者中,癫痫和精神障碍由低钙血症诱发,纠正后可逆转。认知和锥体外系损害似乎与脑内钙化的逐渐扩展有关,尤其是在诊断较晚的患者中。在假性甲状旁腺功能减退症患者中,由于该病特有的其他因素的作用,情况有所不同。

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