Granulomatous polyangiitis misdiagnosed as hematogenous lung abscess: A case report
Abstract Granuloma polyangiitis (GPA) is a necrotizing granulomatous inflammation, which is a systemic autoimmune disease that mainly affects the upper respiratory tract, lungs, and kidneys. Clinically, the clinical manifestations of GPA vary greatly, and it is extremely easy to be misdiagnosed. We...
Main Authors: | Yong Yang, Xiao‐Yue Chang |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2022-12-01
|
Series: | Clinical Case Reports |
Subjects: | |
Online Access: | https://doi.org/10.1002/ccr3.6445 |
Similar Items
-
M2 macrophage is the predominant phenotype in airways inflammatory lesions in patients with granulomatosis with polyangiitis
by: Alexandre Wagner Silva de Souza, et al.
Published: (2017-05-01) -
Microscopic polyangiitis associated with antineutrophil cytoplasmic antibodies: Clinical features
by: T V Beketova
Published: (2015-05-01) -
Antineutrophil cytoplasmic antibody-negative granulomatosis with polyangiitis localized to the lungs
by: Yuichi Ohteru, et al.
Published: (2022-01-01) -
Oral granulomatosis with polyangiitis a systematic review
by: Alberto J. Peraza Labrador, et al.
Published: (2023-02-01) -
GRANULOMATOSIS WITH POLYANGIITIS, WHICH IS PATHOGENETICALLY ASSOCIATED WITH ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES: CLINICAL FEATURES
by: Tatiana Valentinovna Beketova
Published: (2012-12-01)