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起源于蝶窦的颅内侵袭性曲霉病:三例高剂量伊曲康唑成功治疗的病例

Intracranial invasive aspergillosis originating in the sphenoid sinus: a successful treatment with high-dose itraconazole in three cases.

作者信息

Yamanoi Takahiko, Shibano Ken, Soeda Tomoko, Hoshi Akihiko, Matsuura Yutaka, Sugiura Yoshihiro, Endo Kazuhiro, Yamamoto Teiji

机构信息

Department of Neurology, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan.

出版信息

Tohoku J Exp Med. 2004 Jun;203(2):133-9. doi: 10.1620/tjem.203.133.

Abstract

We report three cases of intracranial aspergillosis originating in the sphenoid sinus in immunocompetent patients. The patients presented with an orbital apex syndrome in that a unilateral loss of vision and cranial nerve III palsy were seen in all cases and a contralateral involvement was also seen in one case. Despite the initial treatment with a conventional dose of itraconazole (ITCZ, 200 mg/day), the neurological deficits failed to improve and the granulomatous inflammation was not suppressed. Therefore, we treated with a combination of a high dose of ITCZ at 500-1000 mg/day (16-24 mg/kg/day) and amphotericin B (AMPH-B) at 0.5 mg/kg/day, in conjunction with a pulse dose of methylprednisolone at 1000 mg/day. Two cases responded favorably in that the ocular movements completely recovered, and their maximum serum concentrations of the hydroxy ITCZ were 7816 ng/ml and 5370 ng/ml. However, the other case worsened, despite ITCZ treatment at 16 mg/kg/day, and the serum concentration of the hydroxy ITCZ was 3863 ng/ml. The surgical decompression of the cavernous sinus via an extradural approach was performed, and the dose of ITCZ was increased to 24 mg/kg/day. The resulting serum concentration of the hydroxy ITCZ was 4753 ng/ml, and the outcome of this case has been favorable. These results suggest that a high blood level of the hydroxy ITCZ (more than 4500 ng/ml) is a prerequisite for the successful treatment of intracranial aspergillosis and that the combination treatment of ITCZ with AMPH-B would be preferred. The concomitant use of steroid and/or surgical decompression should be considered, if the invasiveness is not well-controlled in spite of intensive medical therapy.

摘要

我们报告了3例免疫功能正常患者起源于蝶窦的颅内曲霉病。所有患者均表现为眶尖综合征,即均出现单眼视力丧失和动眼神经麻痹,1例还出现对侧受累。尽管最初采用常规剂量的伊曲康唑(ITCZ,200mg/天)治疗,但神经功能缺损未改善,肉芽肿性炎症也未得到抑制。因此,我们采用高剂量ITCZ(500 - 1000mg/天,16 - 24mg/kg/天)与两性霉素B(AMPH - B,0.5mg/kg/天)联合治疗,并联合使用脉冲剂量的甲泼尼龙1000mg/天。2例患者反应良好,眼球运动完全恢复,其羟基伊曲康唑的最大血清浓度分别为7816ng/ml和5370ng/ml。然而,另一例患者尽管接受了16mg/kg/天的ITCZ治疗仍病情恶化,其羟基伊曲康唑的血清浓度为3863ng/ml。通过硬膜外入路对海绵窦进行了手术减压,并将ITCZ剂量增加至24mg/kg/天。由此产生的羟基伊曲康唑血清浓度为4753ng/ml,该病例的结果良好。这些结果表明,高血液水平的羟基伊曲康唑(超过4500ng/ml)是成功治疗颅内曲霉病的先决条件,ITCZ与AMPH - B联合治疗更为可取。如果尽管进行了强化药物治疗侵袭性仍未得到很好控制,则应考虑同时使用类固醇和/或手术减压。

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