Eosinophilic Granulomatosis with Polyangiitis Manifesting as Recurrent Nasal Polyps and Hemorrhagic Necrotic Bullae: A Rare Disease Successfully Treated with Azathioprine
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare multisystemic vasculitis which was previously called Churg-Strauss syndrome or allergic granulomatosis. It has an unknown pathogenesis, possibly autoimmune in nature. As it has a low incidence, there is only scant published literature. T...
Saved in:
Main Authors: | Abdulaziz Alotaibi (Author), Stefan W. Schneider (Author) |
---|---|
Format: | Book |
Published: |
Karger Publishers,
2019-02-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A Classical Manifestation of Eosinophilic Granulomatosis with Polyangiitis with an Unusual Catastrophic Outcome
by: Balachandra S Bhat, et al.
Published: (2024) -
Relevance of cutaneous manifestations and antineutrophil cytoplasmic antibody status in eosinophilic granulomatosis with polyangiitis
by: Meiko Sone, et al.
Published: (2022) -
Koebner Phenomenon in Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss)
by: Maylis Tourte, et al.
Published: (2017) -
Perspectives on the Efficacy of Benralizumab for Treatment of Eosinophilic Granulomatosis With Polyangiitis
by: Yasuhiko Koga, et al.
Published: (2022) -
Eosinophilic granulomatosis with polyangiitis: a challenge for differential diagnosis
by: Elias Forero Illera, et al.
Published: (2018)