C-A Lame1, B Loum2, A-K Fall3, J Cucherousset4, A-R Ndiaye3. 1. Service ORL, Hôpital Principal de Dakar, 11, rue Jean Mermoz, Dakar, Senegal. Electronic address: cheikhlame@gmail.com. 2. Service ORL, Hôpital Principal de Dakar, 11, rue Jean Mermoz, Dakar, Senegal. 3. Service de Médecine interne, Hôpital Principal de Dakar, 11, rue Jean Mermoz, Dakar, Senegal. 4. Service de Pathologie, GHI Le RAINCY-MONTFERMEIL, 10, rue du Général Leclerc, 93370 Montfermeil, France.
Abstract
INTRODUCTION: Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a benign disease most commonly affecting adult females. It generally presents in the form of febrile cervical lymphadenopathy. This diagnosis must be considered in the setting of tropical medicine, dominated by a high prevalence of tuberculous lymphadenitis and haematological malignancies. CASE REPORT: The authors report the case of a 33-year-old Senegalese woman who presented with subacute cervical lymphadenopathy associated with fever and laboratory signs of inflammation. Serological and tuberculosis screening tests were negative. Histopathological examination of a lymph node biopsy, following failure of nonspecific antibiotic therapy, concluded on a diagnosis of Kikuchi-Fujimoto disease. A favourable course was observed in response to corticosteroid therapy. CONCLUSION: In Sub-Saharan Africa, the association of polyadenitis and febrile syndrome, after excluding tuberculosis and lymphomas, must raise the suspicion of rare diseases such as Kikuchi-Fujimoto disease.
INTRODUCTION:Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a benign disease most commonly affecting adult females. It generally presents in the form of febrile cervical lymphadenopathy. This diagnosis must be considered in the setting of tropical medicine, dominated by a high prevalence of tuberculous lymphadenitis and haematological malignancies. CASE REPORT: The authors report the case of a 33-year-old Senegalese woman who presented with subacute cervical lymphadenopathy associated with fever and laboratory signs of inflammation. Serological and tuberculosis screening tests were negative. Histopathological examination of a lymph node biopsy, following failure of nonspecific antibiotic therapy, concluded on a diagnosis of Kikuchi-Fujimoto disease. A favourable course was observed in response to corticosteroid therapy. CONCLUSION: In Sub-Saharan Africa, the association of polyadenitis and febrile syndrome, after excluding tuberculosis and lymphomas, must raise the suspicion of rare diseases such as Kikuchi-Fujimoto disease.
Authors: Claudia Wallrauch; Tom Heller; Bal Mukunda Dhungel; Henry Kayera; Sam Phiri; Tamiwe Monica Tomoka Journal: Malawi Med J Date: 2018-12 Impact factor: 0.875