Dalugama Chamara, Gawarammana Indika Bandara
Department of Medicine, University of Peradeniya, Peradeniya, Sri Lanka.
J Med Case Rep. 2017 Dec 16;11(1):349. doi: 10.1186/s13256-017-1521-y.
Kikuchi Fujimoto disease is an uncommon benign condition of necrotizing histiocytic lymphadenitis commonly seen in East Asian and Japanese populations. It commonly presents with fever, cervical lymphadenopathy, and elevated inflammatory markers. Diagnosis of Kikuchi Fujimoto disease is based on histopathological studies of the involved lymph nodes. The presentation of Kikuchi Fujimoto disease can mimic many sinister conditions including lymphoma. Treatment is mainly supportive provided that accurate diagnosis is made and sinister conditions like lymphoma ruled out.
We report the case of an 18-year-old Sri Lankan Moor woman who presented with fever and cervical lymphadenopathy for 1 month. She had elevated inflammatory markers with high lactate dehydrogenase and ferritin levels. She had an extensive work-up including an excision biopsy of an involved lymph node and bone marrow biopsy. Finally, a diagnosis of Kikuchi Fujimoto disease was based on histopathology of the lymph node and negative bone marrow biopsy.
Although Kikuchi Fujimoto disease is a self-limiting condition, it is a great masquerader which mimics the clinical features of many sinister conditions including tuberculosis, lymphoma, and adult-onset Still's disease. Early recognition of the disease is of crucial importance in minimizing potentially harmful and unnecessary evaluations and treatments.
菊池富士本病是一种罕见的坏死性组织细胞性淋巴结炎良性疾病,常见于东亚和日本人群。其通常表现为发热、颈部淋巴结病及炎症标志物升高。菊池富士本病的诊断基于受累淋巴结的组织病理学研究。菊池富士本病的表现可模仿包括淋巴瘤在内的许多严重疾病。只要做出准确诊断并排除淋巴瘤等严重疾病,治疗主要是支持性的。
我们报告一例18岁斯里兰卡穆尔族女性病例,她发热和颈部淋巴结病1个月。她的炎症标志物升高,乳酸脱氢酶和铁蛋白水平较高。她接受了广泛的检查,包括对受累淋巴结进行切除活检和骨髓活检。最终,根据淋巴结的组织病理学检查及骨髓活检阴性诊断为菊池富士本病。
尽管菊池富士本病是一种自限性疾病,但它很会伪装,可模仿包括结核病、淋巴瘤和成人斯蒂尔病在内的许多严重疾病的临床特征。早期识别该疾病对于尽量减少潜在有害和不必要的评估及治疗至关重要。