Consultant Nephrologist at Healthbay Polyclinic Jumeirah ‒ 1-6 Al Wasl Rd ‒ Umm Al Sheif, Dubai, Emirati Arabi Uniti (UAE).
G Ital Nefrol. 2023 Dec 22;40(6):2023-vol6.
Kikuchi-Fujimoto disease (KFD), or Histiocytic Necrotizing Lymphadenitis, is a rare disease, with worldwide distribution but is best known in Japan and South Asia. The most common feature is cervical lymphadenopathy, accompanied by tenderness or high fever, with night sweats, but it can also be asymptomatic or with a very wide range of symptoms. The diagnosis is histopathological, on excisional biopsy. The Kikuchi-Fujmoto disease can mimic lymphoma but also tuberculosis and some autoimmune diseases, or be associated with them. Nephrologists need to be aware of it, considering the potential renal involvement. The association with systemic lupus erythematosus (SLE) is the most frequent but not the only one. Early diagnosis of this disease can prevent unnecessary investigations and aggressive therapies.
菊池古氏病(KFD),又称组织细胞坏死性淋巴结炎,是一种罕见疾病,全球各地均有分布,但在日本和南亚更为常见。该病最常见的特征是颈部淋巴结病,伴有触痛或高热,盗汗,但也可能无症状或症状非常广泛。诊断依据是组织病理学,通过切除活检。菊池古氏病可模仿淋巴瘤,也可模仿结核病和某些自身免疫性疾病,或与之相关。肾病学家需要意识到这一点,因为该病可能会累及肾脏。该病与系统性红斑狼疮(SLE)的关联最为常见,但并非唯一。早期诊断该病可以避免不必要的检查和激进治疗。