嗜酸性肉芽肿伴多血管炎

V.P. Drobysheva, A.Ar. Demin
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引用次数: 0

摘要

介绍。嗜酸性肉芽肿病合并多血管炎(EGPA),以前称为过敏性肉芽肿病(Churg-Stross综合征),在现代意义上是一种坏死性多系统血管炎,主要是小血管,伴有抗中性粒细胞胞浆抗体(ANCA)的过量产生,外周血嗜酸性粒细胞增多。虽然最常涉及的是呼吸器官(鼻窦炎,支气管哮喘,肺浸润),EGPA影响任何器官和系统(心脏,肾脏,胃肠道,神经系统,皮肤,关节等),这使得其诊断困难。的目标。目的:报告一难以诊断的嗜酸性肉芽肿病合并多血管炎的临床病例。材料和方法。对患者进行了临床、实验室及专项检测分析。结果。该患者的EGPA诊断困难。发热高达40°C,上肢和下肢丘疹性坏死性皮肤疹,躯干;减肥;心、肺、肾、肝多脏器受累;葡萄球菌血培养阳性。溶血,以及葡萄球菌皮肤损伤。表皮病-所有这些都是怀疑葡萄球菌败血症可能伴有感染性心内膜炎的原因,并开出了抗菌治疗,但无效。随着病情进展,临床表现恶化,发现血嗜酸性粒细胞增多(18%),免疫检查ANCA阳性,肌皮瓣组织学检查微血管周围嗜酸性粒细胞和淋巴组织细胞浸润,证实了EGPA的诊断。环磷酰胺和中剂量甲基强的松龙的脉冲化疗导致患者疾病表现的消退。结论。EGPA的过程可包括危及生命的情况(急性心肌梗死和肺出血)。及时的诊断和标准的积极化疗扩大了治疗这类严重患者的可能性。
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EOSINOPHILIC GRANULOMATOSIS WITH POLYANGIITIS
Introduction. Eosinophilic granulomatosis with polyangiitis (EGPA), formerly known as allergic granulomatosis (Churg-Stross syndrome), in the modern sense is a necrotizing multisystem vasculitis of predominantly small vessels associated with hyperproduction of antineutrophil cytoplasmic antibodies (ANCA), peripheral blood hypereosinophilia. Although the most frequently involved are the respiratory organs (rhinosinusitis, bronchial asthma, pulmonary infiltrates), EGPA affects any organs and systems (heart, kidneys, gastrointestinal tract, nervous system, skin, joints, etc.) which makes its diagnosis difficult. Aim. To present an observation of a difficult-to-diagnose clinical case of eosinophilic granulomatosis with polyangiitis. Materials and methods. The analysis of clinical, laboratory, special testing of the patient was carried out. Results. Diagnosis of EGPA in this patient was difficult. Fever up to 40°C, papulo-necrotic skin eruptions on upper and lower extremities, trunk; weight loss; multiple organ involvement of heart, lungs, kidneys, liver; positive hemoculture with isolation of Staph. haemoliticus, and from skin lesions of Staph. epidermidis – all these served as a reason to suspect staphylococcal sepsis with possible infectious endocarditis and prescribe antimicrobial therapy which was ineffective. Progression of the disease with worsening clinical manifestations, detection of blood eosinophilia (18%), positive ANCA on immunological examination, eosinophilic and lymphohistiocytic infiltration around microvessels on histological examination of the musculocutaneous flap allowed the diagnosis of EGPA to be verified. Pulse chemotherapy with cyclophosphamide and medium doses of methylprednisolone led to regression of the disease manifestations in the patient. Conclusion. The course of EGPA can include life-threatening conditions (acute myocardial infarction and pulmonary hemorrhage). Timely diagnosis and standards of active chemotherapy expand possibilities of managing this severe group of patients.
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