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[一名接受桥脑胶质瘤治疗的免疫功能低下患者的非典型假瘤性神经脑膜隐球菌病。病例报告及文献综述]

[Atypical pseudotumoral neuromeningeal cryptococcosis in an immunocompromised patient treated for pontine glioma. Case report and literature review].

作者信息

Palenzuela G, El-Fertit H, Coubes P, Mallié M, Rigau V, Margueritte G

机构信息

Service d'hémato-oncologie pédiatrique, hôpital Arnaud-de-Villeneuve, 371, avenue du Doyen-Gaston-Giraud, 34295, Montpellier cedex 5, France.

出版信息

Neurochirurgie. 2009 Jun;55(3):329-32. doi: 10.1016/j.neuchi.2008.05.002. Epub 2008 Aug 15.

Abstract

BACKGROUND AND PURPOSE

We report an atypical feature of neuromeningeal cryptococcosis presenting as spinal cystic arachnoiditis and cerebellar cryptococcoma in a child treated for pontine glioma.

CASE REPORT

In November 2003, we diagnosed a pontine glioma in a six-year-old female child. She was initially treated with radiotherapy (54Gy for six weeks) and dexamethasone until July 2006. From January 2004 to September 2006, the patient received 30 cycles of chemotherapy including vincristine 1.5mg/m(2) Day 1, carboplatin 150mg/m(2) Day 1, and temozolomide 150mg/m(2) Days 2-6 every 28 days. In October 2006, the patient suffered spontaneous acute low back pain radiating into both lower limbs revealing lumbar cystic arachnoiditis and cerebellar cryptococcoma. The cerebrospinal fluid (CSF) sample showed lymphocytic pleocytosis and Cryptococcus neoformans; glucose and protein levels were low. First-line medical treatment including liposomal amphotericin B, then fluconazole effectively decreased the pain. However, in February 2007, she presented with cauda equina syndrome and the spinal MRI showed that the lumbar cyst had increased in size. The patient underwent a lumbar laminectomy and cyst removal. Histology confirmed the arachnoiditis with no cancer cells or pathogenic agents.

CONCLUSIONS

Arachnoiditis and cryptococcoma are rare. They can appear to be a brain neoplasm because of their pseudotumoral aspect. Often, the diagnosis can be made from the CSF sample.

摘要

背景与目的

我们报告了一例神经脑膜隐球菌病的非典型特征,该病例表现为一名接受脑桥胶质瘤治疗的儿童出现脊髓囊性蛛网膜炎和小脑隐球菌瘤。

病例报告

2003年11月,我们诊断出一名6岁女童患有脑桥胶质瘤。她最初接受了放疗(6周内54Gy)和地塞米松治疗,直至2006年7月。从2004年1月至2006年9月,患者接受了30个周期的化疗,包括每28天一次的长春新碱1.5mg/m²第1天、卡铂150mg/m²第1天以及替莫唑胺150mg/m²第2 - 6天。2006年10月,患者突发急性下背部疼痛并放射至双下肢,显示出腰椎囊性蛛网膜炎和小脑隐球菌瘤。脑脊液(CSF)样本显示淋巴细胞增多以及新型隐球菌;葡萄糖和蛋白质水平较低。包括脂质体两性霉素B,随后氟康唑的一线药物治疗有效减轻了疼痛。然而,2007年2月,她出现马尾综合征,脊柱MRI显示腰椎囊肿增大。患者接受了腰椎椎板切除术和囊肿切除术。组织学证实为蛛网膜炎,未见癌细胞或病原体。

结论

蛛网膜炎和隐球菌瘤较为罕见。由于其假肿瘤样外观,它们可能看似脑肿瘤。通常,可从脑脊液样本中做出诊断。

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