Davis M D, Daoud M S, McEvoy M T, Su W P
Department of Dermatology, Mayo Clinic, Rochester, MN 55905, USA.
J Am Acad Dermatol. 1997 Aug;37(2 Pt 1):199-203. doi: 10.1016/s0190-9622(97)80125-9.
Allergic granulomatosis of Churg-Strauss (Churg-Strauss syndrome) is a distinct clinical disease of multisystem vasculitis.
We characterize the clinical and histologic features of cutaneous findings in Churg-Strauss syndrome.
All patients with Churg-Strauss syndrome seen between 1976 and 1995 were retrospectively reviewed.
Ninety patients with the diagnosis of Churg-Strauss syndrome were identified; 36 (40%) had cutaneous findings. Five patients (6%) had skin lesions as the initial manifestation. The most frequent cutaneous findings were purpura and petechiae on the lower extremities and cutaneous nodules and papules on the elbows. In 37 biopsy specimens from 29 patients, the most common findings were extravascular necrotizing granuloma (15 specimens) and leukocytoclastic vasculitis (16 specimens).
Cutaneous lesions in Churg-Strauss syndrome are common. Their characteristic clinical and histologic pattern may help establish the diagnosis.
变应性肉芽肿性血管炎(Churg-Strauss综合征)是一种独特的多系统血管炎临床疾病。
我们描述Churg-Strauss综合征皮肤表现的临床和组织学特征。
对1976年至1995年间诊治的所有Churg-Strauss综合征患者进行回顾性研究。
确诊为Churg-Strauss综合征的患者有90例;36例(40%)有皮肤表现。5例(6%)以皮肤病变为首发表现。最常见的皮肤表现为下肢紫癜和瘀点以及肘部皮肤结节和丘疹。在来自29例患者的37份活检标本中,最常见的表现为血管外坏死性肉芽肿(15份标本)和白细胞破碎性血管炎(16份标本)。
Churg-Strauss综合征中的皮肤病变很常见。其特征性的临床和组织学表现可能有助于确诊。