Dwivedi Mamta, Singh Shruti, Tripathi Anjani K, Singh Mrityunjaya, Rani Deepa
Pathology, King George's Medical University, Lucknow, IND.
General Surgery, Prasad Institute of Medical Science and Hospital, Lucknow, IND.
Cureus. 2025 May 4;17(5):e83462. doi: 10.7759/cureus.83462. eCollection 2025 May.
Kikuchi-Fujimoto disease (KFD) is a frequently febrile, self-limited, subacute necrotizing lymphadenitis. It occurs predominantly in young females and is more common in Asia.
This study aims to characterize the cytomorphological spectrum of KFD through fine-needle aspiration (FNA) findings across multiple centers, highlight under-recognized diagnostic features, and refine cytologic differentials to improve diagnostic accuracy.
The study group comprised a multicenter study experience of 30 cases diagnosed as KFD on cytology or subsequent histology.
Cytomorphological features of 30 cases diagnosed as KFD on FNA smears were studied. Out of these 30 cases, spontaneous resolution occurred on 4 to 16 weeks of follow-up in 22 cases; in the remaining eight cases, cytologic diagnosis was confirmed on histology, supplemented by immunohistochemistry.
The cytological features of KFD pose diagnostic challenges, on account of its broad cytologic spectrum, though crescentic histiocytes are a constant feature. These cytological features must be interpreted in the appropriate clinical context.
菊池-藤本病(KFD)是一种常伴有发热、自限性的亚急性坏死性淋巴结炎。该病主要发生于年轻女性,在亚洲更为常见。
本研究旨在通过多中心细针穿刺(FNA)结果来描述KFD的细胞形态学谱,突出未被充分认识的诊断特征,并完善细胞学鉴别诊断以提高诊断准确性。
研究组包括30例经细胞学或后续组织学诊断为KFD的多中心研究经验。
对30例经FNA涂片诊断为KFD的病例的细胞形态学特征进行了研究。在这30例病例中,22例在随访4至16周后自发缓解;其余8例经组织学确诊,免疫组化辅助诊断。
KFD的细胞学特征因其广泛的细胞谱而带来诊断挑战,尽管新月形组织细胞是其恒定特征。这些细胞学特征必须在适当的临床背景下进行解读。