Kikuchi-Fujimoto disease associated with a flare-up of a leukocytoclastic vasculitis: A rare case report and review of literature

被引:1
作者
Sandakly, Nicolas [1 ,2 ]
El Koubayati, Georgio [1 ,2 ]
Sarkis, Jeannette [1 ,2 ]
Naderi, Samah [3 ]
Sebaaly, Delivrance [1 ,3 ]
Haddad, Fady [2 ]
机构
[1] Lebanese Univ, Fac Med Sci, Hadath Campus, Hadath, Lebanon
[2] Geitaoui Univ, Lebanese Hosp, Med Ctr, Dept Internal Med, Beirut, Lebanon
[3] Geitaoui Univ, Lebanese Hosp, Med Ctr, Dept Pathol, Beirut, Lebanon
关键词
Kikuchi-Fujimoto; leukocytoclastic vasculitis; lymphadenopathy; HISTIOCYTIC NECROTIZING LYMPHADENITIS;
D O I
10.1097/MD.0000000000037626
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale:Kikuchi-Fujimoto disease (KFD) also known as histiocytic necrotizing lymphadenopathy is an exceedingly rare cause of cervical lymphadenopathy, commonly accompanied by systemic symptoms such as fever, fatigue, night sweats, myalgia, skin rash.Patient concerns:In this paper, we report the case of a 22-year-old female patient who experienced a flare-up of leukocytoclastic vasculitis that was complicated by the appearance of a cervical lymph node with dysphagia, fever and nausea.Diagnosis:Infectious and autoimmune workup came back negative.Interventions:Excisional lymph node biopsy was done and the pathology results were consistent with histiocytic necrotizing lymphadenitis in keeping with Kikuchi-Fujimoto disease.Outcomes:Patient improved on intravenous corticosteroids and was discharged on per os prednisone. Six month follow-up shows complete resolution of her symptoms.Lessons:KFD should be ruled out in patients with autoimmune or inflammatory diseases who develop lymphadenopathies.
引用
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页数:5
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