Resumen
Introduction: ANCA-associated vasculitides (AAV) are
characterized by inflammation of small caliber blood vessels and a high percentage of
positivity for antineutrophil cytoplasmic antibodies (ANCA).Clinical case: It is a case of a
74-year-old mestizo man, with dysphonia, weight loss, superficial erythematous lesions
distributed in lower limbs. One week prior to admission, he presented rectal bleeding,
diffuse abdominal pain with clinical data of hypovolemic shock, ulcerative colitis was
identified (colonoscopy) and positive serology for PR3-ANCA. Immunosuppressive treatment was
started with favorable evolution.Conclusion: AAV have variable clinical phenotypes with
forms from mild to fulminant, they should be suspected early, treated promptly to favorably
influence their prognosis.
| Idioma original | Español |
|---|---|
| Publicación | Revista de la Facultad de Ciencias Médicas de la Universidad de Cuenca |
| Estado | Publicada - 2022 |
| Publicado de forma externa | Sí |
Palabras clave
- Granulomatosis con poliangitis; Vasculitis; Hemorragia; Patología