Chronic skin lichenification as an unusual presentation of eosinophilic granulomatosis with polyangiitis: case report and literature review

被引：0

作者：

Sbrana, F. ^{[1
]}

Loggini, B. ^{[2
]}

Galimberti, S. ^{[3
]}

Coceani, M. ^{[1
]}

Latorre, M. ^{[4
]}

Seccia, V ^{[5
]}

L'Abbate, S. ^{[6
]}

Mosca, M. ^{[6
]}

Pasanisi, E. M. ^{[1
]}

Baldini, C. ^{[6
]}

机构：

[1] Fdn Toscana Cabriele Monasterio, Pisa, Italy

[2] Univ Pisa, Inst Pathol Anat, I-56100 Pisa, Italy

[3] Univ Pisa, Dept Oncol Transplants & New Med Tech, Hematol Unit, I-56100 Pisa, Italy

[4] Univ Pisa, Cardio Thorac & Vasc Dept, I-56100 Pisa, Italy

[5] Azienda Osped Univ Pisana, Ear Nose Throat Unit 1, Rome, Italy

[6] Univ Pisa, UO Rheumatol, Dept Internal Med, I-56100 Pisa, Italy

来源：

ACTA REUMATOLOGICA PORTUGUESA | 2016年 / 41卷 / 02期

关键词：

Chronic skin lichenification; Eosinophilic; Granulomatosis with Polyangiitis; Hypereosinophilic syndrome; CHURG-STRAUSS-SYNDROME; RAPIDLY PROGRESSIVE GLOMERULONEPHRITIS; ALLERGIC GRANULOMATOSIS; BLOOD EOSINOPHILIA; LIMITED FORM; ANGIITIS; CLASSIFICATION; ASTHMA; MASS;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Eosinophilic granulomatosis with polyangiitis (EGPA) is an uncommon ANCA-associated systemic small-vessel necrotizing vasculitis. At times, EGPA presenting manifestations can be very different from the usually recognized disease patterns. We report a 52-year-old female patient with 3 years history of itching. In this period, the patient developed chronic skin lichenification on her legs followed by full-blown ANCA-MPO positive EGPA in combination with blood hypereosinophilia, eosinophilic vasculitis at skin biopsy, subclinical asthma and chronic rhinosinusitis.

引用

页码：158 / 161

页数：4

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