Müller Cornelia S L, Vogt Thomas, Becker Sören L
Department of Dermatology, Saarland University Medical Center, Homburg/Saar, Germany.
Institute of Medical Microbiology and Hygiene, Saarland University Medical Center, Homburg/Saar, Germany.
Am J Dermatopathol. 2021 Mar 1;43(3):202-208. doi: 10.1097/DAD.0000000000001764.
Kikuchi-Fujimoto disease (KFD) is a necrotizing histiocytic lymphadenitis that was described for the first time in 1972 in Japan. Its etiology is still not fully understood. It has been reported in association with many different agents, diseases, and triggering factors without any conclusive result. To the best of our knowledge, we report for the first time a case of KFD with systemic lupus erythematosus in a child in association with a polymerase chain reaction (PCR)-positive throat swab for Mycoplasma pneumoniae. Although difficult to prove, the acute M. pneumoniae infection might have served as a triggering event for the development of KFD in our case. We encourage further studies to investigate a potential relationship between KFD and M. pneumoniae, which should also use PCR-based testing for this pathogen in patients with KFD.
菊池-藤本病(KFD)是一种坏死性组织细胞性淋巴结炎,1972年在日本首次被描述。其病因仍未完全明确。已有报道称它与许多不同的病原体、疾病及触发因素有关,但尚无定论。据我们所知,我们首次报告了一名患有系统性红斑狼疮的儿童同时患有菊池-藤本病,且其咽拭子聚合酶链反应(PCR)检测显示肺炎支原体呈阳性。虽然难以证实,但在我们的病例中,急性肺炎支原体感染可能是菊池-藤本病发生的触发事件。我们鼓励进一步开展研究,以调查菊池-藤本病与肺炎支原体之间的潜在关系,在菊池-藤本病患者中对该病原体进行检测时也应采用基于PCR的检测方法。