Sais G, Vidaller A, Jucglà A, Servitje O, Condom E, Peyri J
Department of Dermatology, Hospital Princeps d'Espanya, Ciutat Sanitària i Universitària de Bellvitge, Barcelona, Spain.
Arch Dermatol. 1998 Mar;134(3):309-15. doi: 10.1001/archderm.134.3.309.
To analyze risk factors for systemic involvement and long-term course in leukocytoclastic vasculitis.
A clinicopathological study of 160 patients with leukocytoclastic vasculitis followed up for at least 3 years. Univariate and multivariate analysis were conducted by logistic regression methods.
The Bellvitge Hospital, a referral center in Barcelona, Spain.
One hundred sixty patients with cutaneous leukocytoclastic vasculitis. Patients in the categories cutaneous/systemic vasculitis and acute/chronic cutaneous vasculitis were selected for comparative analysis.
Clinical, laboratory, and histopathological findings.
Of 89 females and 71 males, aged 14 to 89 years, systemic involvement was documented in 20% of cases. Perinuclear-staining antineutrophil cytoplasmic autoantibodies were found in 21% of patients and cryoglobulins in 25.4%. Of the patients, 1.9% died of systemic vasculitis. The average duration of cutaneous lesions was 27.9 months. In 67.2%, a cause or associated condition was identified. Of the skin specimens, 59.6% showed vasculitis limited to superficial dermal vessels. Direct immunofluorescence was positive in 84.3% of cases. In the multivariate analysis, paresthesia, fever, and absence of painful lesions were found to be risk factors for systemic involvement. Cryoglobulins, arthralgia, and normal temperature were risk factors for chronic cutaneous disease.
Our results identify prognostic factors in leukocytoclastic vasculitis and may provide some aid in the management of this heterogeneous group of patients.
分析白细胞破碎性血管炎全身受累及长期病程的危险因素。
对160例白细胞破碎性血管炎患者进行临床病理研究,随访至少3年。采用逻辑回归方法进行单因素和多因素分析。
西班牙巴塞罗那的转诊中心贝尔维奇医院。
160例皮肤白细胞破碎性血管炎患者。选择皮肤/系统性血管炎和急性/慢性皮肤血管炎类别中的患者进行比较分析。
临床、实验室和组织病理学检查结果。
89例女性和71例男性,年龄14至89岁,20%的病例有全身受累记录。21%的患者发现核周染色抗中性粒细胞胞浆自身抗体,25.4%的患者发现冷球蛋白。1.9%的患者死于系统性血管炎。皮肤病变的平均持续时间为27.9个月。67.2%的患者确定了病因或相关疾病。59.6%的皮肤标本显示血管炎局限于浅表真皮血管。直接免疫荧光在84.3%的病例中呈阳性。多因素分析中,感觉异常、发热和无疼痛性病变是全身受累的危险因素。冷球蛋白、关节痛和体温正常是慢性皮肤疾病的危险因素。
我们的结果确定了白细胞破碎性血管炎的预后因素,可能有助于对这一异质性患者群体的管理。