Caesar-Peterson Shannon, Yoon Dosuk, Tulla Katrina, Nahidi Seyed M, Tickoo Sharang, Sheikh Mudnia, Depaz Hector
Wyckoff Heights Medical Center, Brooklyn, NY, USA.
J Surg Case Rep. 2021 Oct 12;2021(10):rjab442. doi: 10.1093/jscr/rjab442. eCollection 2021 Oct.
Kikuchi-Fujimoto disease (KFD) is a rare lymphohistiocytic disorder with an unknown etiopathogenesis. Due to its non-specific lymphadenopathy presentation, treatment is complicated by the frequency by which it is misdiagnosed-for example up to one-third of cases are misdiagnosed as malignant lymphoma, leading to expensive clinical testing and overtreatment of this typically self-limiting illness. KFD has a strong association with SLE, although its transience and rarity make it difficult to investigate. We present a case of KFD to illustrate the variance in presentation and typical outcome of KFD. We want to increase awareness and shed some light on some typical and atypical clinical presentations of KFD to reduce the incidence of misdiagnosis.
菊池-藤本病(KFD)是一种病因不明的罕见淋巴细胞组织细胞增生性疾病。由于其淋巴结病表现不具特异性,常被误诊,这使得治疗变得复杂——例如,高达三分之一的病例被误诊为恶性淋巴瘤,导致对这种通常为自限性疾病进行昂贵的临床检查和过度治疗。KFD与系统性红斑狼疮(SLE)密切相关,尽管其短暂性和罕见性使其难以研究。我们报告一例KFD病例,以说明KFD临床表现的差异和典型转归。我们希望提高对KFD一些典型和非典型临床表现的认识,以减少误诊率。