Atypical manifestations of granulomatosis with polyangiitis: the diagnostic challenge for pulmonologists

被引:7
|
作者
Szymanowska-Narloch, Amelia [1 ]
Gawryluk, Dariusz [2 ]
Blasinska-Przerwa, Katarzyna [3 ]
Sieminska, Alicja [1 ]
机构
[1] Med Univ Gdansk, Dept Allergol, Gdansk, Poland
[2] Natl TB & Lung Dis Res Inst, Dept Lung Dis 1, Warsaw, Poland
[3] Natl TB & Lung Dis Res Inst, Dept Radiol, Warsaw, Poland
关键词
granulomatosis with polyangiitis; atypical manifestations; diagnosis; therapy; vasculitis; NERVOUS-SYSTEM INVOLVEMENT; WEGENERS-GRANULOMATOSIS; CARDIAC INVOLVEMENT; HYPERTROPHIC PACHYMENINGITIS; INTESTINAL INVOLVEMENT; BREAST INVOLVEMENT; DIABETES-INSIPIDUS; BACK-PAIN; ANCA; PERIAORTITIS;
D O I
10.5603/ARM.2019.0062
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
This is a review considering atypical manifestations of granulomatosis with polyangiitis (GPA). Virtually any organ can be affected, and in some patients, GPA can manifest unusually. Since thoracic involvement of GPA often predominates, the first who might be expected to establish a diagnosis are pulmonary specialists. We would like to familiarize pulmonary specialists with several extra-ELK (E: ear-nose-throat; L: lung; K: kidney) involvements of the disease. We describe sites rarely affected by GPA like the breast, skeletal system, orbit and eye, heart and vessels, central nervous system, urogenital system as well as endocrine and gastrointestinal tract involvement.
引用
收藏
页码:244 / 253
页数:10
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