Churg-Strauss's Syndrome; Review of literature

B. Adefuye, P. Adefuye, O. Odusan, S. Ogun, O. Ogunsemi, T. Olunuga
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Abstract

Churg – Strauss Syndrome (CSS) is a rare idiopathic, multisystemic, autoimmune disease, characterized by diffuse eosinophilic infiltration and necrotizing vasculitis of small to medium sized vessels. Late onset asthma and/or allergic rhinitis are frequent clinical manifestations with fever and loss of weight as systemic symptoms at presentation. Mononeuritis multiplex, myalgia, skin involvement (purpura, skin nodules, urticarial rash, livedo reticularis), arthralgia, gastro intestinal tract (GIT) involvement, pericardial, myocardial, central nervous system (CNS) and renal involvements are other manifestations of CSS. Diagnostic hallmarks include Blood and tissue eosinophilia, histology revealing eosinophilic granulomas and/or necrotizing vasculitides in tissue biopsy. Although not a criterion of CSS diagnosis, presence of Antineutrophil Cytoplasmic Antibodies (ANCA), especially antimyeloperoxidase (ANCA MPO), is associated with CSS. This is present in more than 40% (40 - 66 - 73%) of CSS patients. Pathogenesis varies from ANCA activation of neutrophils and resultant systemic endothetial damage (in ANCA positive CSS), on one hand, and tissue infiltration by eosinophils with resultant tissue damage by toxic products of eosinophils (in ANCA negative CSS), on the other hand. There are also the varying B and T cell dysfunctions. Diffuse organ involvement, especially cardiovascular (CVS), GIT, rare involvement of CNS and renal system suggest poorer prognosis and possible fatal outcome. Patients with these poor prognostic outlooks, especially cardiac, receive aggressive treatment using corticosteroids combined with immunosuppresants (chiefly cyclophosphamide). Patients with refractory CSS have been successfully treated, adding TNF – alpha blockers to a combination of glucocorticoids and cyclophosphamide. Antithymocyte globulin or pooled intravenous globulin have been found effective alternative therapy in resistant cases and most especially in pregnant patients. Keywords: Churg-Strauss syndrome, Eosinophilia, Antineutrophil Cytoplasmic Antibodies, Immunosuppressants
Churg-Strauss综合征;文献综述
Churg - Strauss综合征(CSS)是一种罕见的特发性多系统自身免疫性疾病,以弥漫嗜酸性粒细胞浸润和中小血管坏死性血管炎为特征。迟发性哮喘和/或过敏性鼻炎是常见的临床表现,首发时伴有发热和体重减轻等全身性症状。多发性单神经炎、肌痛、皮肤受累(紫癜、皮肤结节、荨麻疹、网状红斑)、关节痛、胃肠道(GIT)受累、心包、心肌、中枢神经系统(CNS)和肾脏受累是CSS的其他表现。诊断标志包括血液和组织嗜酸性粒细胞增多,组织活检显示嗜酸性肉芽肿和/或坏死性血管增生。虽然不是CSS的诊断标准,但抗中性粒细胞胞浆抗体(ANCA),特别是抗髓过氧化物酶(ANCA MPO)的存在与CSS相关。超过40%(40 - 66 - 73%)的CSS患者存在这种情况。发病机制不同,一方面是ANCA激活中性粒细胞并导致全身内源性损伤(在ANCA阳性CSS中),另一方面是嗜酸性粒细胞浸润组织,由嗜酸性粒细胞的毒性产物导致组织损伤(在ANCA阴性CSS中)。还有不同的B细胞和T细胞功能障碍。弥漫性脏器受累,尤其是心血管(CVS)、GIT,少见的中枢神经系统和肾脏受累提示预后较差,可能导致死亡。这些预后不良的患者,尤其是心脏患者,接受皮质类固醇联合免疫抑制剂(主要是环磷酰胺)的积极治疗。难治性CSS患者已成功治疗,在糖皮质激素和环磷酰胺联合使用TNF - α阻滞剂。抗胸腺细胞球蛋白或汇集静脉球蛋白已被发现有效的替代治疗耐药病例,尤其是在怀孕患者。关键词:Churg-Strauss综合征,嗜酸性粒细胞增多症,抗中性粒细胞胞浆抗体,免疫抑制剂
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