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首页> 外文期刊>European journal of pediatrics >Acute febrile neutrophilic dermatosis (Sweet's syndrome) in childhood and adolescence: two new patients and review of the literature on associated diseases.
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Acute febrile neutrophilic dermatosis (Sweet's syndrome) in childhood and adolescence: two new patients and review of the literature on associated diseases.

机译:儿童和青春期急性发热性中性粒细胞性皮肤病(Sweet's综合征):两名新患者,有关疾病的文献综述。

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OBJECTIVES: The objectives of this study were to analyse the literature on Sweet's syndrome in childhood focussing on associated diseases and to suggest possible screening procedures for this group of patients. Furthermore, two new patients with Sweet's syndrome are reported. METHODS: A literature search was performed on Pub med using search terms "sweet* syndrome*" and neutrophil* dermatos*. Patients were subdivided into the following groups: classic/idiopathic, paraneoplastic, and parainflammatory Sweet's syndrome. RESULTS: The literature search revealed 64 patients (including our two patients) who were diagnosed with Sweet's syndrome in childhood and adolescence; 27 (42%) patients were categorized as "classic/idiopathic Sweet's syndrome". In 37 patients (58%) chronic associated diseases were reported. Out of these, 21 (33%) patients were categorized as "parainflammatory Sweet's syndrome" including chronic recurrent multifocal osteomyelitis, vasculitis with aortitis, recurrent infections due to immunodeficiencies, arthritis, and systemic lupus erythematosus. Sixteen (25%) patients were categorized as "paraneoplastic Sweet's syndrome" comprising both malignant and premalignant diseases like leukemia, aplastic anaemia, and Fanconi anaemia. As all five (8%) patients treated with drugs (granulocyte-colony stimulating factor, retinoid acid) suffered from malignant, premalignant, or parainflammatory diseases, these patients were categorized according to the underlying disease. Two new children with Sweet's syndrome and associated diseases are presented here, one of them suffering from recurrent infections and trisomy 21, while the other was diagnosed with CNS vasculitis 5(1/2) years after the primary diagnosis. CONCLUSIONS: Sweet's syndrome should be considered in differential diagnosis of prolonged fever with cutaneous involvement. As most cases of pediatric Sweet's syndrome are associated with other diseases we suggest careful screening and monitoring of these patients especially concerning malignant/premalignant diseases, immunodeficiencies, cardiovascular involvement, autoimmune diseases, and drug associations.
机译:目的:本研究的目的是分析有关儿童期Sweet's综合征的文献,重点是相关疾病,并提出针对该组患者的可能的筛查程序。此外,据报道有两名新的Sweet氏综合症患者。方法:使用检索词“ sweet * syndrome *”和嗜中性粒细胞* dermatos *在Pub med上进行文献检索。将患者分为以下几类:经典/特发性,副肿瘤性和副炎症性Sweet综合征。结果:文献检索发现64例儿童(包括我们的两名患者)在儿童和青少年时期被诊断出患有Sweet综合征。 27名(42%)患者被归类为“经典/特发性Sweet综合征”。在37例患者(58%)中报告了慢性相关疾病。在这些患者中,有21名(33%)被归类为“副炎症性Sweet's综合征”,包括慢性复发性多灶性骨髓炎,血管炎伴主动脉炎,由于免疫缺陷,关节炎和系统性红斑狼疮引起的反复感染。十六名(25%)患者被分类为“副肿瘤性Sweet综合征”,包括恶性和恶变前疾病,如白血病,再生障碍性贫血和Fanconi贫血。由于接受药物(粒细胞集落刺激因子,类维生素A酸)治疗的所有五名患者(8%)都患有恶性,恶变前或副炎症性疾病,因此将这些患者根据潜在疾病进行分类。此处介绍了两个患有Sweet's综合征和相关疾病的新儿童,其中一个患有反复感染和21三体性,而另一个在初次诊断后5(1/2)年被诊断出患有CNS血管炎。结论:在皮肤受累长期发热的鉴别诊断中应考虑Sweet氏综合症。由于大多数儿童Sweet's综合征病例都与其他疾病有关,因此我们建议对这些患者进行仔细的筛查和监测,尤其是有关恶性/恶变前疾病,免疫缺陷,心血管受累,自身免疫性疾病和药物关联的患者。

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