P-ANCA negative eosinophilic granulomatosis with polyangiitis.


Journal

Respiratory medicine case reports
ISSN: 2213-0071
Titre abrégé: Respir Med Case Rep
Pays: England
ID NLM: 101604463

Informations de publication

Date de publication:
2019
Historique:
received: 19 01 2019
revised: 24 03 2019
accepted: 25 03 2019
entrez: 17 4 2019
pubmed: 17 4 2019
medline: 17 4 2019
Statut: epublish

Résumé

Vasculitis refers to inflammation of the systemic vessels. Eosinophilic granulomatosis with polyangiitis (EGPA) is a medium and small vessel vasculitis characterized by hypereosinophilia, pulmonary infiltrates, difficult to treat asthma and polyneuropathies. Diagnosis can often be challenging. In this article, we present a case of a young lady who was diagnosed ANCA negative EGPA.

Identifiants

pubmed: 30989049
doi: 10.1016/j.rmcr.2019.100830
pii: S2213-0071(19)30027-9
pii: 100830
pmc: PMC6446216
doi:

Types de publication

Case Reports

Langues

eng

Pagination

100830

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Auteurs

Saad Ullah (S)

Department of Pulmonary and Critical Care Medicine, Southern Illinois University, Springfield, IL, USA.

Mirza Ali (M)

Department of Internal Medicine, Southern Illinois University, Springfield, IL, USA.

Phyo Kyaw (P)

Department of Pulmonary and Critical Care Medicine, Southern Illinois University, Springfield, IL, USA.

Faraaz Nayeemuddin (F)

Department of Pulmonary and Critical Care Medicine, Southern Illinois University, Springfield, IL, USA.

Rajagopal Sreedhar (R)

Department of Pulmonary and Critical Care Medicine, Southern Illinois University, Springfield, IL, USA.

John Gao (J)

Department of Pathology, Southern Illinois University, Springfield, IL, USA.

Classifications MeSH