菊池-藤本--一种神秘而罕见的疾病:3 个病例的报告和文献简评。

IF 1.4 4区 医学 Q3 RHEUMATOLOGY ARP Rheumatology Pub Date : 2024-09-01
Joana Victor Lage, Ana Teresa Guerra, Francisca Costa, Andreia Martins, Paula Correia, Catarina Luis
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引用次数: 0

摘要

菊池-藤本氏病(KFD)是一种罕见的良性疾病,主要特征是发热和淋巴结病。尽管随着时间的推移进行了许多研究,但其病因仍不清楚,感染和自身免疫过程被假定为主要病因。我们报告了三例菊地-藤本氏病。所有患者均为女性,表现为发热和颈淋巴结病。为了排除感染性疾病、自身免疫性疾病和淋巴增生性疾病,我们进行了广泛的检查。诊断是通过淋巴结切除活检和组织病理学检查确定的。所有患者都接受了医学随访,其中一人患上了系统性红斑狼疮(SLE)。
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Kikuchi-Fujimoto - an enigmatic and rare disease: a report of 3 cases and brief review of the literature.

Kikuchi-Fujimoto disease (KFD) is a rare and benign condition mainly characterized by fever and lymphadenopathies. Although many studies have been carried out over time, its aetiology remains unclear, with infectious and autoimmune processes being hypothesized as the main causes. We report three cases of Kikuchi-Fujimoto disease. All patients were female and presented with fever and cervical lymphadenopathies. Extensive work up was performed, in order to rule out infectious, autoimmune and lymphoproliferative diseases. The diagnosis was established through lymph node excisional biopsy and histopathological examination. All patients were followed-up in a medical appointment, with one developing systemic lupus erythematosus (SLE).

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Kikuchi-Fujimoto - an enigmatic and rare disease: a report of 3 cases and brief review of the literature. Systematic literature review to inform the Portuguese recommendations for the management of Raynaud's phenomenon and digital ulcers in systemic sclerosis and other connective tissue diseases. Lessons learnt from the recent recommendations for the non-pharmacological management of systemic sclerosis. Predictors of efficacy of ultrasound-guided intra-articular glucocorticoid injection in knee osteoarthritis: A prospective study. Beyond rheumatoid nodules in rheumatoid arthritis.
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