Punith S B, Agarwal Ayush, Garg Divyani, Garg Ajay, Shamim Shamim A, Mallick Saumya Ranjan, Gupta Pranjal, Srivastava Achal K
Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Department of Neuroimaging and Interventional Neuroradiology, All India Institute of Medical Sciences, New Delhi, India.
Ann Indian Acad Neurol. 2025 Jan 1;28(1):116-119. doi: 10.4103/aian.aian_498_24. Epub 2024 Oct 8.
Kikuchi-Fujimoto disease (KFD) is a rare benign condition associated with fever and lymphadenopathy and was first described by Kikuchi and Fujimoto independently in 1972 as histiocytic necrotizing lymphadenitis. The diagnosis is made by histopathology with immunohistochemistry. Limbic encephalitis is an extremely rare presentation of this uncommon disease, which has been described mainly in children. Available evidence is sparse in the form of case reports and case series in the form of 10 cases published till date. We report a case of an adult female with KFD with autoimmune limbic encephalitis, who had complete clinical and radiologic recovery with treatment, and a literature review of all the cases published till date.
菊池-藤本病(KFD)是一种与发热和淋巴结病相关的罕见良性疾病,1972年菊池和藤本分别首次将其描述为组织细胞性坏死性淋巴结炎。诊断通过组织病理学及免疫组织化学检查。边缘叶脑炎是这种罕见疾病极为罕见的一种表现形式,主要在儿童中有所描述。目前以病例报告和病例系列(迄今已发表10例)形式存在的证据稀少。我们报告一例患有自身免疫性边缘叶脑炎的成年女性菊池-藤本病患者,经治疗后临床和影像学完全恢复,并对迄今已发表的所有病例进行文献综述。