Kikuchi-Fujimoto disease: A rare case of pyrexia of unknown origin

Vishal Sadatia, Mayank Thakker, Devang Ambaliya
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Abstract

A young male was referred to a clinician for a complaint of fever of short duration with non-specific joint pain and treated for 1 week but after some time again presented with the same complaints with severe epigastric tenderness and vomiting. There was no past medical history before this episode. When cervical lymph node biopsy was performed gave us the diagnosis of histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease). A rare form of necrotizing lymphadenitis is an uncommon, benign, self-limiting disorder of obscure etiology. It affects mostly young adults of both genders. Clinically, it presents with fever and lymphadenopathy of a firm to rubbery consistency frequently involving cervical lymph nodes while weight loss, splenomegaly, and leukopenia in severely ill patients.
菊池-藤本氏病:不明原因热病的罕见病例
一名年轻男性因短时间发热并伴有非特异性关节疼痛而被转诊至临床医生处,接受了一周的治疗,但一段时间后再次出现同样的症状,并伴有严重的上腹部压痛和呕吐。在此之前没有任何病史。在进行颈淋巴结活检时,我们诊断他患了组织细胞坏死性淋巴结炎(菊池-藤本氏病)。组织细胞坏死性淋巴结炎是一种罕见的良性自限性疾病,病因不明。它主要影响男女青壮年。临床表现为发热、淋巴结肿大,质地坚硬或呈橡皮样,常累及颈淋巴结,重症患者会出现体重减轻、脾脏肿大和白细胞减少。
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