Sheikh Junaid Zafar, Kila Louay, Amin Irfan, Khan Umar, Casserly Brian
Respiratory Medicine, University Hospital Limerick, Limerick, IRL.
Cureus. 2024 Nov 3;16(11):e72921. doi: 10.7759/cureus.72921. eCollection 2024 Nov.
Kikuchi-Fujimoto disease (KFD) is a rare self-limiting condition presenting as fever and cervical lymphadenopathy, with only two reported cases with isolated mediastinal lymphadenopathy. Lack of awareness about this condition often results in a high rate of misdiagnosis. We present a case of a 29-year-old Indian male with fever, mucocutaneous ulcers, weight loss, and mediastinal lymphadenopathy on CT. Extensive investigations ruled out malignancy and autoimmune and infectious causes. Endobronchial ultrasound-guided fine needle aspiration revealed necrotizing lymphadenitis, indicating KFD, followed by symptomatic management and reassurance. Awareness is crucial to avoid misdiagnosis and unnecessary treatment due to its potentially serious differentials. Long-term follow-up is imperative due to its association with autoimmune conditions.
菊池-藤本病(KFD)是一种罕见的自限性疾病,表现为发热和颈部淋巴结病,仅有两例孤立性纵隔淋巴结病的报道病例。对这种疾病认识不足常常导致误诊率很高。我们报告一例29岁的印度男性病例,该患者有发热、黏膜皮肤溃疡、体重减轻,CT显示纵隔淋巴结病。广泛检查排除了恶性肿瘤、自身免疫性和感染性病因。支气管内超声引导下细针穿刺显示坏死性淋巴结炎,提示为菊池-藤本病,随后进行了对症治疗并给予患者安慰。鉴于其可能存在的严重鉴别诊断,提高认识对于避免误诊和不必要的治疗至关重要。由于它与自身免疫性疾病有关,长期随访势在必行。