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[菊池-藤本病诊断前后的神经系统并发症:疾病的罕见表现还是额外诊断的线索?]

[NEUROLOGIC COMPLICATIONS AROUND THE DIAGNOSIS OF KIKUCHI-FUJIMOTO DISEASE: A RARE PRESENTATION OF THE DISEASE OR A HINT OF AN ADDITIONAL DIAGNOSIS?].

作者信息

Ghantous Nassem, Hershkovic Shimrit, Poran Itamar, Benninger Felix, Molad Yair, Eliakim-Raz Noa

机构信息

Department of Medicine E, Rabin Medical Center- Beilinson, Petah Tikva, Israel.

Department of Neurology, Rabin Medical Center- Beilinson, Petah Tikva, Israel.

出版信息

Harefuah. 2021 May;160(5):307-310.

PMID:34028223
Abstract

Neurologic symptoms are an extremely rare presentation of Kikuchi-Fujimoto disease. We report a case of a young female patient diagnosed with Kikuchi-Fujimoto disease, presenting with neurologic symptoms compatible with aseptic meningitis, along with radiographic findings which improved with steroidal treatment. Despite the rarity of these findings, they were reported as part of the disease manifestation, however, since Kikuchi-Fujimoto disease is associated with other diseases, such as systemic lupus erythematosus (SLE), other diagnoses cannot be ruled out.

摘要

神经系统症状是菊池-藤本病极为罕见的表现形式。我们报告一例年轻女性患者,被诊断为菊池-藤本病,表现出与无菌性脑膜炎相符的神经系统症状,同时影像学检查结果经类固醇治疗后有所改善。尽管这些表现罕见,但仍被报告为该疾病的表现之一,然而,由于菊池-藤本病与其他疾病相关,如系统性红斑狼疮(SLE),因此不能排除其他诊断。

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