Kurihara Mutsuka, Yanagita Yasutaka, Yokokawa Daiki, Li Yu, Ikusaka Masatomi
Department of General Medicine, Chiba University Hospital, Chiba, Japan.
Eur J Case Rep Intern Med. 2024 Jan 25;11(2):004258. doi: 10.12890/2024_004258. eCollection 2024.
Kikuchi-Fujimoto disease (KFD), also called histiocytic necrotizing lymphadenitis, is more common in young women and typically presents with small, painful, localized cervical lymphadenopathy that resolves spontaneously within a few weeks. Laboratory findings are variable. As many as 40% of KFD cases are reported to be painless, and up to 22% to be generalized lymphadenopathy. Therefore, malignant lymphoma could be a differential diagnosis of KFD. A histopathologic diagnosis is needed when it is difficult to distinguish KFD from lymphoma. KFD typically shows small, highly accumulated cervical lymph nodes on fluorodeoxyglucose positron emission tomography (FDG-PET). This contrasts with malignant lymphoma, which tends to be associated with massive lymphadenopathy. In our case, a 40-year-old Japanese male presented with painless lumps in the right neck, accompanied by fever, night sweats, and loss of appetite. His symptoms and laboratory results worsened over a month. FDG-PET revealed highly accumulated uptake in cervical, mediastinal, and axillary lymph nodes. The PET imaging showed a small, high FDG uptake and contributed to the correct diagnosis of KFD. This case report highlights the importance of FDG-PET, which is a valuable diagnostic tool for KFD as it typically differentiates large clusters of small lymph nodes typical of KFD from normal lymph nodes.
Kikuchi-Fujimoto disease (KFD) typically presents with small, painful, localised cervical lymphadenopathy.KFD has atypical patterns showing painless and generalised lymphadenopathy.Fluorodeoxyglucose positron emission tomography (FDG-PET) could be useful for diagnosing not only malignant lymphoma but also KFD.
菊池-藤本病(KFD),也称为组织细胞坏死性淋巴结炎,在年轻女性中更为常见,通常表现为颈部局限性小而疼痛的淋巴结病,数周内可自行缓解。实验室检查结果各不相同。据报道,多达40%的KFD病例无痛,高达22%为全身性淋巴结病。因此,恶性淋巴瘤可能是KFD的鉴别诊断。当难以区分KFD和淋巴瘤时,需要进行组织病理学诊断。KFD在氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)上通常显示颈部淋巴结小且高度聚集。这与恶性淋巴瘤形成对比,后者往往与大量淋巴结病相关。在我们的病例中,一名40岁的日本男性右侧颈部出现无痛性肿块,伴有发热、盗汗和食欲不振。他的症状和实验室检查结果在一个月内恶化。FDG-PET显示颈部、纵隔和腋窝淋巴结有高度聚集的摄取。PET成像显示FDG摄取量小且高,有助于正确诊断KFD。本病例报告强调了FDG-PET的重要性,它是诊断KFD的一种有价值的工具,因为它通常能将KFD典型的小淋巴结大簇与正常淋巴结区分开来。
菊池-藤本病(KFD)通常表现为颈部局限性小而疼痛的淋巴结病。KFD有非典型表现,包括无痛性和全身性淋巴结病。氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)不仅对诊断恶性淋巴瘤有用,对诊断KFD也有用。