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Case Report: Angioimmunoblastic T-cell lymphoma initially diagnosed as eosinophilic granulomatosis with polyangiitis
CASE REPORT article Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1716129 This article is part of the Research TopicCase Reports in Pulmonary Medicine 2025View all 30 articles Introduction Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis characterized by asthma, chronic rhinosinusitis, peripheral blood eosinophilia, and necrotizing vasculitis.
Phenotypes contribute to treatments
Chronic obstructive pulmonary disease (COPD) is now considered a markedly complex and heterogeneous disease [1]. In the latest update of the Global Initiative for Chronic Obstructive Lung Disease (GOLD 2017) [2], the definition of COPD has been revised to emphasise the heterogeneity of this disease. The phrase “airway and/or alveolar abnormalities” replaces “an enhanced chronic inflammation” in the definition of GOLD 2016.
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