Joean Oana, Thiele Thea, Raap Mieke, Schmidt Reinhold E, Stoll Matthias
Department of Immunology and Rheumatology.
Department of Pathology, Hannover Medical University, Hannover, Germany.
Clin Pract. 2018 Dec 12;8(4):1095. doi: 10.4081/cp.2018.1095. eCollection 2018 Oct 26.
Generalized lymphadenopathy is a common cause of concern for both patients and clinicians. Possible etiologies include infections, malignancies and autoimmune diseases. Kikuchi Fujimoto disease (KFD) is a hyperergic condition that presents with fever, lymphadenopathy and can include systemic involvement, thus being easily mistaken for the above-mentioned entities. We report the case of a previously healthy 18- year old male who presented with a selflimiting generalized lymphadenopathy, high fevers, skin vasculitis and polyserositis. The lymph-node biopsy revealed a histiocytotic necrotizing lymphadenitis, suggestive of Kikuchi's disease. This case emphasizes the importance of KFD in the differential diagnosis of lymphadenopathy, especially in young adults.
全身淋巴结肿大是患者和临床医生共同关注的常见原因。可能的病因包括感染、恶性肿瘤和自身免疫性疾病。菊池富士本病(KFD)是一种超敏性疾病,表现为发热、淋巴结肿大,可累及全身,因此容易与上述疾病混淆。我们报告一例既往健康的18岁男性病例,该患者出现自限性全身淋巴结肿大、高热、皮肤血管炎和多浆膜炎。淋巴结活检显示组织细胞性坏死性淋巴结炎,提示为菊池病。该病例强调了菊池富士本病在淋巴结肿大鉴别诊断中的重要性,尤其是在年轻成年人中。