A Case of Eosinophilic Granulomatosis with Polyangiitis Mimicking Cutaneous Tuberculosis and Tuberculous Lymphadenitis
Malaysian Journal of Dermatology
; : 20-24, 2022.
Article
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| WPRIM
| ID: wpr-962094
Biblioteca responsable:
WPRO
ABSTRACT
Summary@#Eosinophilic granulomatosis with polyangiitis (EGPA), or Churg-Strauss Syndrome (CSS) is a rare granulomatous necrotizing vasculitic disease characterized by the presence of asthma, sinusitis, and hypereosinophilia. We describe a patient who was initially diagnosed with tuberculous lymphadenitis and later diagnosed with EGPA.
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Índice:
WPRIM
Asunto principal:
Tuberculosis Cutánea
/
Tuberculosis Ganglionar
/
Granulomatosis con Poliangitis
Idioma:
En
Revista:
Malaysian Journal of Dermatology
Año:
2022
Tipo del documento:
Article