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与系统性红斑狼疮相关的菊池-藤本病:病例报告及文献复习

Kikuchi-Fujimoto's disease associated with systemic lupus erythematosus: case report and review of the literature.

作者信息

Santana Alex, Lessa Bruno, Galrão Liliana, Lima Isabella, Santiago Mittermayer

机构信息

Hospital Santa Izabel, Núcleo de Reumatologia da Bahia/Escola Bahiana de Medicina e Saúde Pública (EBMSP), Praça Almeida Couto, 500, CEP 40.000-000 Nazaré, Salvador, Bahia, Brazil.

出版信息

Clin Rheumatol. 2005 Feb;24(1):60-3. doi: 10.1007/s10067-004-0923-6. Epub 2004 Oct 27.

Abstract

Kikuchi-Fujimoto's disease (KFD) or histiocytic necrotising lymphadenitis is a benign and self-limited disease, of unknown aetiology, which affects mainly young women. It presents with localised lymphadenopathy, predominantly in the cervical region, accompanied by fever and leukopenia in up to 50% of the cases. KFD has been rarely described in association with systemic lupus erythematosus (SLE), and its diagnosis can precede, postdate or coincide with the diagnosis of SLE. We present a patient with the diagnosis of SLE characterised by arthritis, leukopenia, malar rash, photosensitivity and positive ANA, besides cervical lymphadenopathy whose biopsy was compatible with KFD, which improved after using prednisone. Although the presence of lymphadenopathy is not uncommon in SLE patients, particularly in the phases of disease activity, the concomitance with KFD has rarely been reported in the literature. Its recognition is necessary because one can avoid laborious investigation for infectious and lymphoproliferative diseases.

摘要

菊池-藤本病(KFD)或组织细胞坏死性淋巴结炎是一种病因不明的良性自限性疾病,主要影响年轻女性。其表现为局限性淋巴结病,主要位于颈部区域,高达50%的病例伴有发热和白细胞减少。KFD很少与系统性红斑狼疮(SLE)相关联描述,其诊断可先于、后于或与SLE的诊断同时出现。我们报告一名诊断为SLE的患者,其特征为关节炎、白细胞减少、颧部皮疹、光过敏和抗核抗体阳性,此外还有颈部淋巴结病,其活检结果与KFD相符,使用泼尼松后病情改善。虽然淋巴结病在SLE患者中并不少见,尤其是在疾病活动期,但KFD与之并存的情况在文献中很少报道。认识到这一点很有必要,因为这样可以避免对感染性和淋巴增殖性疾病进行费力的检查。

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