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Sweet 综合征患者伴或不伴恶性肿瘤:来自一个三级学术转诊中心的 83 例患者的回顾性分析。

Sweet syndrome in patients with and without malignancy: A retrospective analysis of 83 patients from a tertiary academic referral center.

机构信息

Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

Department of Medicine, Division of Hematology and Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

J Am Acad Dermatol. 2018 Feb;78(2):303-309.e4. doi: 10.1016/j.jaad.2017.09.013. Epub 2017 Oct 26.

Abstract

BACKGROUND

Sweet syndrome is a neutrophilic dermatosis that may be categorized into classic, malignancy-associated, and drug-induced subtypes. Few studies have systematically analyzed this rare disorder.

OBJECTIVE

To describe the clinicopathologic characteristics and treatment of Sweet syndrome and identify characteristics associated with concurrent malignancy.

METHODS

We retrospectively reviewed patients with Sweet syndrome at the University of Pennsylvania from 2005 to 2015.

RESULTS

We identified 83 patients (mean age, 57 years; 51% male) with Sweet syndrome: 30% with the classic form, 44% with the malignancy-associated form, 24% with the drug-induced form in the setting of malignancy, and 2% with the drug-induced form. Acute myeloid leukemia was the most common malignancy (in 24 of 83 patients [29%]). Filgrastim was the most common medication (used in 8 of 83 patients [10%]). Leukopenia (P < .001), anemia (P = .002), thrombocytopenia (P < .001), absence of arthralgia (P < .001), and histiocytoid or subcutaneous histopathology (P = .024) were associated with malignancy (χ test).

LIMITATIONS

This was a retrospective study that represents patients from a single tertiary academic referral center, which may limit its generalizability to other settings.

CONCLUSION

When caring for patients with Sweet syndrome, dermatologists should be aware of the potential association of leukopenia, anemia, thrombocytopenia, absence of arthralgia, and histiocytoid or subcutaneous histopathology with malignancy.

摘要

背景

Sweet 综合征是一种中性粒细胞皮肤病,可分为经典型、恶性肿瘤相关型和药物诱导型。很少有研究系统地分析这种罕见疾病。

目的

描述 Sweet 综合征的临床病理特征和治疗方法,并确定与并发恶性肿瘤相关的特征。

方法

我们回顾性分析了 2005 年至 2015 年期间在宾夕法尼亚大学就诊的 Sweet 综合征患者。

结果

我们共确定了 83 例 Sweet 综合征患者(平均年龄 57 岁,51%为男性):30%为经典型,44%为恶性肿瘤相关型,24%为恶性肿瘤相关药物诱导型,2%为药物诱导型。急性髓系白血病是最常见的恶性肿瘤(83 例患者中有 24 例[29%])。非格司亭是最常见的药物(83 例患者中有 8 例[10%])。白细胞减少(P <.001)、贫血(P =.002)、血小板减少(P <.001)、无关节痛(P <.001)和组织细胞样或皮下组织病理学(P =.024)与恶性肿瘤相关(卡方检验)。

局限性

这是一项回顾性研究,代表了来自单一三级学术转诊中心的患者,这可能限制了其在其他环境中的普遍性。

结论

皮肤科医生在治疗 Sweet 综合征患者时,应注意白细胞减少、贫血、血小板减少、无关节痛和组织细胞样或皮下组织病理学与恶性肿瘤之间的潜在关联。

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