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[婴儿期多发性颅内结核瘤]

[Multiple intracranial tuberculomas in infancy].

作者信息

Serrano M, Campistol J, Chávez B, Caritg J, Fortuny C, Costa J M

机构信息

Servicio de Neurología; Hospital Sant Joan de Déu, Esplugues de Llobregat, 08950, España.

出版信息

Rev Neurol. 2001;33(1):44-6.

Abstract

INTRODUCTION

Tuberculous involvement of the CNS is most frequent in children aged between 6 months and 6 years, although it may occur at any age. It may present as meningoencephalitis, basal arachnoiditis or intracranial tuberculomas. Whilst meningitis is typical of infancy, tuberculomas and arachnoiditis are commoner in adults. It has been estimated that tuberculomas make up 3% of the cases of neurotuberculosis. The increasing use of CAT and MR has been a great help for diagnosis of this serious complication of tuberculosis.

CLINICAL CASE

A 5 month old patient presented with tuberculous meningitis which had been treated with streptomycin, isoniazid, pyrazinamide and rifampicin at the usual dosage. One month later, after good initial progress, triventricular hydrocephaly was diagnosed and a ventriculoperitoneal shunt inserted. Three months after this, there was an episode of intracranial hypertension. Cranial CAT showed considerable zones of hypodense parenchyma without ventricle dilatation. On MR there were multiple, disseminated, rounded areas which were hyperintense on T2 and compatible with intracranial tuberculomas. After fresh insertion of a ventricular shunt, the patient progressed but still had a residual right hemiparesia and retarded development.

CONCLUSIONS

Although intracranial tuberculomas usually occur in adults, they may be seen in children following meningoencephalitis. Occasionally, following a good initial response to tuberculostatic drugs, tuberculomas appear, although not present before, as happened in our patient. This usually occurs within the first three months, and although the mechanism is unknown, it is believed to be due to the accumulation of lymphocytes and macrophages at preexisting microscopic foci when treatment is started.

摘要

引言

中枢神经系统结核受累在6个月至6岁的儿童中最为常见,不过在任何年龄都可能发生。其表现形式可为脑膜脑炎、基底蛛网膜膜炎或颅内结核瘤。脑膜炎在婴儿期较为典型,而结核瘤和蛛网膜膜炎在成人中更为常见。据估计,结核瘤占神经结核病例的3%。计算机断层扫描(CAT)和磁共振成像(MR)的日益广泛应用对诊断这种严重的结核并发症有很大帮助。

临床病例

一名5个月大的患者患结核性脑膜炎,已按常规剂量用链霉素、异烟肼、吡嗪酰胺和利福平进行治疗。一个月后,在初期病情进展良好之后,诊断出三脑室积水并插入了脑室腹腔分流管。在此之后三个月,出现了颅内高压发作。头颅CAT显示有相当大的低密度实质区,脑室无扩张。磁共振成像显示有多个散在的圆形区域,在T2加权像上呈高信号,符合颅内结核瘤表现。再次插入脑室分流管后,患者病情有所好转,但仍有右侧偏瘫后遗症且发育迟缓。

结论

虽然颅内结核瘤通常发生于成人,但在脑膜脑炎后的儿童中也可见到。偶尔,在对抗结核药物最初反应良好之后,会出现此前不存在的结核瘤,就像我们的患者那样。这通常发生在头三个月内,尽管其机制尚不清楚,但据信是由于开始治疗时淋巴细胞和巨噬细胞在先前存在的微小病灶处积聚所致。

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