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导致脑脊液鼻漏的颅底骨淋巴管瘤。

Lymphangioma of the skull base bones leading to cerebrospinal fluid rhinorrhea.

作者信息

Ito Eiji, Saito Kiyoshi, Nagatani Tetsuya, Teranishi Masaaki, Kamei Yuzuru, Yagi Shunjiro, Kawabe Takashi, Niimi Norihiro, Yoshida Jun

机构信息

Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

J Neurosurg Pediatr. 2008 Oct;2(4):273-6. doi: 10.3171/PED.2008.2.10.276.

Abstract

Lymphangioma localized to the bones of the skull base is rare. The authors report herein the case of a 5-year-old boy who presented with lymphangioma of the bone, localized to the skull base and leading to cerebrospinal fluid (CSF) rhinorrhea with meningitis. Neuroimaging demonstrated lytic destruction with a cyst in the right middle skull base. The patient was successfully treated with resection of the tumor and prevention of CSF leakage. Histopathological examination revealed a lymphangioma. An enlarging lymphangioma can lead to bone destruction. A differential diagnosis of a lytic lesion for a cyst at the skull base is important for proper case management.

摘要

局限于颅底骨的淋巴管瘤很罕见。本文作者报告了一例5岁男孩,其患有局限于颅底骨的骨淋巴管瘤,并导致脑脊液鼻漏伴脑膜炎。神经影像学显示右侧中颅底有溶骨性破坏并伴有囊肿。患者通过肿瘤切除和预防脑脊液漏得到了成功治疗。组织病理学检查显示为淋巴管瘤。不断增大的淋巴管瘤可导致骨质破坏。对颅底囊肿样溶骨性病变进行鉴别诊断对正确的病例管理很重要。

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