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菊池-藤本病,非洲淋巴结病的罕见病因。塞内加尔首例病例描述及文献综述。

Kikuchi-Fujimoto disease, a rare cause of lymphadenopathy in Africa. Description of the first case in Senegal and review of the literature.

作者信息

Lame C-A, Loum B, Fall A-K, Cucherousset J, Ndiaye A-R

机构信息

Service ORL, Hôpital Principal de Dakar, 11, rue Jean Mermoz, Dakar, Senegal.

Service ORL, Hôpital Principal de Dakar, 11, rue Jean Mermoz, Dakar, Senegal.

出版信息

Eur Ann Otorhinolaryngol Head Neck Dis. 2017 Oct;134(5):347-349. doi: 10.1016/j.anorl.2017.02.007. Epub 2017 Mar 6.

DOI:10.1016/j.anorl.2017.02.007
PMID:28279633
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.

摘要

引言

菊池-藤本病,即组织细胞坏死性淋巴结炎,是一种最常影响成年女性的良性疾病。它通常表现为发热性颈部淋巴结病。在以结核性淋巴结炎和血液系统恶性肿瘤高发为特征的热带医学背景下,必须考虑到这一诊断。

病例报告

作者报告了一名33岁塞内加尔女性的病例,该患者表现为亚急性颈部淋巴结病,并伴有发热和炎症实验室指标。血清学和结核病筛查试验均为阴性。在非特异性抗生素治疗无效后,对淋巴结活检进行组织病理学检查,确诊为菊池-藤本病。对皮质类固醇治疗反应良好。

结论

在撒哈拉以南非洲,排除结核病和淋巴瘤后,若出现多腺炎和发热综合征,必须怀疑菊池-藤本病等罕见疾病。

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