Clinical laboratory · 2025
A Rare Case of Kikuchi-Fujimoto Disease Complicated with Hemophagocytic Lymphohistiocytosis.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Sun Yingying, Wu Chengcheng, Liu Chunyan, Shao Zonghong
Аннотация
BACKGROUND: Kikuchi-Fujimoto disease (KFD) is a benign, self-limited, rare disease that rarely coexists with hemophagocytic lymphohistiocytosis (HLH).
METHODS: We reported a case of a young female who presented with recurrent fever accompanied by painful lymphadenopathy, joint pain, and skin rash.
RESULTS: Excisional biopsy of lymph node indicated KFD. The clinical symptoms, along with the laboratory findings met the diagnostic criteria for HLH. The patient recovered after receiving glucocorticoid and supportive care.
CONCLUSIONS: The combination of KFD and HLH exhibits distinct clinical characteristics and prognosis. Clinicians should be aware of this condition and avoid inappropriate diagnostic and therapeutic interventions.
METHODS: We reported a case of a young female who presented with recurrent fever accompanied by painful lymphadenopathy, joint pain, and skin rash.
RESULTS: Excisional biopsy of lymph node indicated KFD. The clinical symptoms, along with the laboratory findings met the diagnostic criteria for HLH. The patient recovered after receiving glucocorticoid and supportive care.
CONCLUSIONS: The combination of KFD and HLH exhibits distinct clinical characteristics and prognosis. Clinicians should be aware of this condition and avoid inappropriate diagnostic and therapeutic interventions.