Kosch M, Schmid K W, Hausberg M, Rahn K H, Kisters K
Medizinische Poliklinik, Westfälische Wilhelms-Universität Münster.
Dtsch Med Wochenschr. 1999 Feb 26;124(8):213-6. doi: 10.1055/s-2007-1024276.
A 49-year-old, otherwise healthy woman had recurrent fever and lymphadenopathy with leukopenia for nineteen years. Her symptoms prompted successless antibiotic therapy and extensive evaluations of fever of unknown origin. At admission there were several enlarged cervical lymph nodes and subfebrile temperatures.
Neither laboratory findings nor imaging did show an infectious, rheumatologic or hematologic cause of her symptoms. Histopathological examination of an lymph node biopsy revealed histiocytic, necrotizing lymphadenitis (Kikuchi-Fusimoto disease) as the underlying disease.
After spontaneous resolution without specific therapy the patient is now symptomless and well 9 months after diagnosis.
Kikuchi-Fusimoto disease is a cause of benign and usually self-limiting lymphadenopathy. Clinicians and pathologists should be aware of this uncommon differential diagnosis since early histologic recognition will minimize potentially and unnecessary evaluations and treatments.
一名49岁、其他方面健康的女性反复发热、淋巴结肿大伴白细胞减少达19年。她的症状促使进行了抗生素治疗但未成功,并对不明原因发热进行了广泛评估。入院时,有多个颈部淋巴结肿大及低热。
实验室检查结果及影像学检查均未显示其症状有感染、风湿或血液学病因。淋巴结活检的组织病理学检查显示,组织细胞性坏死性淋巴结炎(菊池-富本病)为潜在病因。
未经特殊治疗自行缓解后,患者在诊断9个月后无症状且状况良好。
菊池-富本病是良性且通常为自限性淋巴结病的一个病因。临床医生和病理学家应了解这种不常见的鉴别诊断,因为早期组织学识别将最大限度减少潜在的不必要评估和治疗。