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The Spectrum of Paraneoplastic Cutaneous Vasculitis in a Defined Population: Incidence and Clinical Features

机译:确定人群中副肿瘤性皮肤血管炎的频谱:发病率和临床特征

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Abstract: Cutaneous vasculitis may be associated with malignancies, and may behave as a paraneoplastic syndrome. This association has been reported in a variable proportion of patients depending on population selection. We conducted the current study to assess the frequency, clinical features, treatment, and outcome of paraneoplastic vasculitis in a large unselected series of 766 patients with cutaneous vasculitis diagnosed at a single university hospital. Sixteen patients (10 men and 6 women; mean age ± standard deviation, 67.94 ± 14.20 yr; range, 40–85 yr) presenting with cutaneous vasculitis were ultimately diagnosed as having an underlying malignancy. They constituted 3.80% of the 421 adult patients. There were 9 hematologic and 7 solid underlying malignancies. Skin lesions were the initial clinical presentation in all of them, and the median interval from the onset of cutaneous vasculitis to the diagnosis of the malignancy was 17 days (range, 8–50 d). The most frequent skin lesions were palpable purpura (15 patients). Other clinical manifestations included constitutional syndrome (10 patients) and arthralgia and/or arthritis (4 cases). Hematologic cytopenias (11 cases) as well as immature peripheral blood cells (6 cases) were frequently observed in the full blood cell count, especially in those with vasculitis associated with hematologic malignancies. Specific treatment for vasculitis was prescribed in 10 patients; nonsteroidal antiinflammatory drugs (4 patients), corticosteroids (3 patients), chloroquine (1 patient), antihistamines (1 patient), and cyclophosphamide (1 patient). Ten patients died due to the malignancy and 6 patients recovered following malignancy therapy. Patients with paraneoplastic vasculitis were older, more frequently had constitutional syndrome, and less frequently had organ damage due to the vasculitis than the remaining patients with cutaneous vasculitis. In summary, cutaneous paraneoplastic vasculitis is an entity not uncommonly encountered by clinicians. The most common underlying malignancy is generally hematologic. In these cases the presence of cytopenias and immature cells may be red flags for the diagnosis of cancer. In patients with paraneoplastic cutaneous vasculitis, the prognosis depends on the underlying neoplasia.
机译:摘要:皮肤血管炎可能与恶性肿瘤有关,可能表现为副肿瘤综合征。根据人群选择,已经报道了这种比例的患者比例可变。我们进行了一项当前研究,以评估在一家大学医院中诊断出的一系列766例皮肤血管炎患者的大量未选择的副肿瘤旁血管炎的发生率,临床特征,治疗和结局。最终被诊断出患有皮肤血管炎的患者(10名男性和6名女性;平均年龄±标准偏差,67.94±14.20岁;范围40-85岁)。他们占421名成人患者的3.80%。有9例血液学和7例潜在的基础恶性肿瘤。皮肤病变是所有病变的最初临床表现,从皮肤血管炎发作到诊断出恶性肿瘤的中位间隔为17天(范围8-50 d)。最常见的皮肤病变是可触及的紫癜(15例)。其他临床表现包括体质综合征(10例)和关节痛和/或关节炎(4例)。血液细胞减少症(11例)和未成熟的外周血细胞(6例)在全血细胞计数中经常被观察到,特别是在那些患有血液系统恶性肿瘤的血管炎患者中。规定对10名患者进行血管炎的特殊治疗;非甾体类抗炎药(4例),皮质类固醇(3例),氯喹(1例),抗组胺药(1例)和环磷酰胺(1例)。 10例患者因恶性肿瘤死亡,6例患者因恶性肿瘤而康复。与其余的皮肤血管炎患者相比,副肿瘤性血管炎患者年龄更大,更容易出现体质综合症,并且因血管炎而导致器官损害的频率更低。总之,皮肤副肿瘤性血管炎是临床医生经常遇到的一个问题。最常见的潜在恶性肿瘤通常是血液学的。在这些情况下,血细胞减少症和未成熟细胞的存在可能是诊断癌症的危险信号。在副肿瘤性皮肤血管炎患者中,预后取决于潜在的肿瘤。

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