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枕部皮样囊肿伴皮窦继发小脑脓肿:病例报告

Cerebellar abscesses secondary to occipital dermoid cyst with dermal sinus: case report.

作者信息

Akhaddar Ali, Jiddane Mohamed, Chakir Noureddine, El Hassani Rachid, Moustarchid Brahim, Bellakhdar Fouad

机构信息

Department of Neuroradiology, Hospital des Spécialités, Rabat, Morocco.

出版信息

Surg Neurol. 2002 Sep-Oct;58(3-4):266-70. doi: 10.1016/s0090-3019(02)00847-9.

DOI:10.1016/s0090-3019(02)00847-9
PMID:12480239
Abstract

BACKGROUND

Hydrocephalus and cerebellar abscesses as the principal manifestations of posterior fossa dermoid cyst are rare. In addition, extradural dermoid cyst of the posterior fossa has been described in only 9 cases in the literature. We present an unusual case of obstructive hydrocephalus due to cerebellar abscesses induced by an adjacent extradural dermoid cyst with complete occipital dermal sinus.

CASE DESCRIPTION

A 14-month-old child presented with acute raised intracranially pressure, seizures, and meningitis. Neuroradiological studies revealed cerebellar cysts with ring enhancement associated with a contiguous occipital cyst, with compression of the adjacent cisterns and the fourth ventricle causing hydrocephalus. The diagnosis of cerebellar abscesses with congenital occipital defect was briefly entertained. The patient was treated by radical excision of the occipital cyst with hair contents, the dermal sinus, and the abscesses through a suboccipital approach, followed by systemic antibiotic therapy with a good outcome. Pathologic examination revealed a dermoid cyst.

CONCLUSION

Posterior fossa dermoid cyst should be considered in all children with occipital skin lesions, especially dermal sinus. CT scan and MRI are the methods of choice for further investigation of suspect congenital dermal lesions. Neurosurgical treatment of these malformations should be planned early to prevent the high incidence of infections such as bacterial meningitis and cerebellar abscess. Clinical presentation, diagnostic evaluation, and treatment of these rare lesions are reviewed.

摘要

背景

以脑积水和小脑脓肿为后颅窝皮样囊肿主要表现的情况较为罕见。此外,文献中仅报道了9例后颅窝硬膜外皮样囊肿。我们报告了1例不寻常的病例,该病例因相邻的伴有完整枕部皮窦的硬膜外皮样囊肿引发小脑脓肿导致梗阻性脑积水。

病例描述

一名14个月大的儿童出现急性颅内压升高、癫痫发作和脑膜炎症状。神经放射学检查显示小脑囊肿伴有环形强化,与相邻的枕部囊肿相连,压迫相邻脑池和第四脑室导致脑积水。曾一度考虑诊断为伴有先天性枕部缺损的小脑脓肿。通过枕下入路对含有毛发的枕部囊肿、皮窦和脓肿进行根治性切除,随后进行全身抗生素治疗,患者预后良好。病理检查显示为皮样囊肿。

结论

对于所有有枕部皮肤病变,尤其是皮窦的儿童,均应考虑后颅窝皮样囊肿。CT扫描和MRI是进一步检查可疑先天性皮肤病变的首选方法。应尽早规划对这些畸形的神经外科治疗,以预防细菌性脑膜炎和小脑脓肿等感染的高发生率。本文对这些罕见病变的临床表现、诊断评估及治疗进行了综述。

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