Anemia Combined Significantly Increased High-Sensitivity C Reactive Protein and Lung Lesions Lead to the Diagnosis of Granulomatosis with Polyangiitis Proven by Lung Biopsy and Anti-neutrophil Cytoplasmic Antibody Test

被引:3
作者
Ge, Yan L. [1 ]
Liu, Cong H. [2 ]
Wang, Meng H. [3 ]
Zhang, Jia B. [1 ]
Chen, Hao [4 ]
Zhu, Xiao Y. [1 ]
Li, Zhen Z. [1 ]
Li, Hong L. [1 ]
Cui, Zi Y. [1 ]
Li, Li Q. [1 ]
Fu, Ai S. [1 ]
Wang, Hong Y. [1 ]
机构
[1] North China Univ Sci & Technol, Affiliated Hosp, Dept Resp Med, Jianshe Rd 73, Tangshan 063000, Hebei, Peoples R China
[2] North China Univ Sci & Technol, Affiliated Hosp, Dept Endocrinol Med, Tangshan, Hebei, Peoples R China
[3] North China Univ Sci & Technol, Affiliated Hosp, Dept Hosp Informat Management, Tangshan, Hebei, Peoples R China
[4] North China Univ Sci & Technol, Affiliated Hosp, Dept Cardiovasc Med, Tangshan, Hebei, Peoples R China
关键词
granulomatosis with polyangiitis; anti-neutrophil cytoplasmic antibody; anemia; hs-CRP;
D O I
10.7754/Clin.Lab.2018.180733
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: To report an atypical case misdiagnosed as lung abscess over the past 2 months, but persistent anemia combined with significantly increased hs-CRP and lung lesions indicated systemic lesion, which led to the diagnosis of granulomatosis with polyangiitis proven by lung biopsy and anti-neutrophil cytoplasmic antibody test (ANCA). Methods: The complete blood count, hs-CRP, and anti-neutrophil cytoplasmic antibody (ANCA) test were performed. The pathology consultation for the lung biopsy was arranged. Results: Hemoglobin was 8.5 g/L, hs-CRP was > 200 mg/L, c-ANCA directed against anti-proteinase 3 (PR3) was positive, pathology consultation reported granulomatous inflammation. Conclusions: When patients have multiple organ dysfunction combined with anemia and significantly increased hs-CRP, physicians should pay attention to systemic vasculitis.
引用
收藏
页码:187 / 189
页数:3
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