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脑型惠普尔病的长期随访

Long-term follow-up in cerebral Whipple's disease.

作者信息

Schnider P J, Reisinger E C, Gerschlager W, Müller C, Berger T, Krejs G J, Auff E

机构信息

Department of Neurology, University of Vienna, Austria.

出版信息

Eur J Gastroenterol Hepatol. 1996 Sep;8(9):899-903.

PMID:8889458
Abstract

OBJECTIVE

To evaluate the long-term outcome in patients with cerebral Whipple's disease.

PATIENTS

We reviewed the literature and contacted authors who had reported on cerebral Whipple's disease within the last 10 years. Fifteen patients were evaluated, including one patient treated at our hospital and the one presented in this paper. The mean observation period was 41 +/- 37 months (minimum 1 month, maximum 120 months).

RESULTS

Four patients had improved and were able to pursue an independent lifestyle, three patients had improved but are still dependent on help with simple activities of daily life, one patient was unchanged, and seven patients had died. Patients with initial penicillin alone had a worse prognosis than patients with initial penicillin plus streptomycin.

CONCLUSION

Third generation cephalosporins have been shown to be beneficial in cerebral Whipple's disease, therefore initial antibiotic treatment of Whipple's disease should consist of ceftriaxone (instead of penicillin) combined with streptomycin. Since five of 12 patients (40%) treated with co-trimoxazole (trimethoprim plus sulphamethoxazole) did not respond, we conclude that the combination of trimethoprim and sulphamethoxazole does not prevent or cure central nervous system (CNS) involvement in all patients with Whipple's disease. If CNS relapse occurs during treatment with trimethoprim and sulphamethoxazole, oral third generation cephalosporins might be a useful alternative.

摘要

目的

评估脑型惠普尔病患者的长期预后。

患者

我们查阅了文献,并联系了在过去10年内报告过脑型惠普尔病的作者。共评估了15例患者,包括我院治疗的1例患者以及本文所报告的1例患者。平均观察期为41±37个月(最短1个月,最长120个月)。

结果

4例患者病情改善,能够独立生活;3例患者病情改善,但仍需依赖他人协助进行简单的日常生活活动;1例患者病情无变化;7例患者死亡。初始仅使用青霉素治疗的患者预后比初始使用青霉素加链霉素治疗的患者差。

结论

已证明第三代头孢菌素对脑型惠普尔病有益,因此惠普尔病的初始抗生素治疗应采用头孢曲松(而非青霉素)联合链霉素。由于12例接受复方新诺明(甲氧苄啶加磺胺甲恶唑)治疗的患者中有5例(40%)无反应,我们得出结论,甲氧苄啶和磺胺甲恶唑联合用药并不能预防或治愈所有惠普尔病患者的中枢神经系统(CNS)受累。如果在甲氧苄啶和磺胺甲恶唑治疗期间发生CNS复发,口服第三代头孢菌素可能是一种有用的替代治疗方法。

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