From:  Eosinophilic granulomatosis with polyangiitis: overcoming diagnostic obstacles and exploring pharmacotherapeutic approaches

 Rewinding the crucial facts for better understanding.

AspectsFacts
DefinitionVasculitis, a rare autoimmune disease, is characterized by eosinophilia and inflammation of blood vessels.
EtiologyUnknown; may be caused by a mix of environmental stimuli and genetic predisposition.
EpidemiologyPrevalence: 10–13 per million; more common in middle-aged adults, with slight male predominance.
PathophysiologyInvolves Th2-mediated immune response, eosinophilic infiltration, and ANCA (anti-neutrophil cytoplasmic antibodies) positivity in some cases.
Clinical featuresAsthma, eosinophilia, vasculitis symptoms (e.g., purpura, neuropathy), and organ involvement (e.g., heart, lungs, kidneys).
Diagnostic criteria1. Asthma 2. Eosinophilia > 10% 3. Sinusitis 4. Pulmonary infiltrates 5. Vasculitis 6. Extravascular eosinophils.
Laboratory findingsElevated eosinophils, positive ANCA (in 40–60% of cases), elevated IgE, increased inflammatory markers (ESR, CRP).
Imaging studiesChest X-ray and CT scan showing pulmonary infiltrates, sinusitis, and sometimes cardiomegaly.
Biopsy findingsVasculitis with eosinophil infiltration in tissue (such as the skin or lungs) occurs in.
Differential diagnosisChurg-strauss syndrome, Wegener’s granulomatosis, hypereosinophilic syndrome, and allergic bronchopulmonary aspergillosis.
Treatment optionsCorticosteroids, immunosuppressants such as cyclophosphamide or azathioprine, and biologics.
Therapeutic approachesThe treatment of eosinophilic vasculitis should be done with a stepwise approach beginning with corticosteroids and/or other medications such as bronchodilators and oxygen to help with symptoms. If the patient has severe or refractory symptoms, immunosuppressants or immunotherapy should be added.
PrognosisGenerally good outcomes with treatment, the 5-year survival rate is > 80%. Long-term complications are possible. Patients are also at risk of relapse.
ComplicationsPatients may experience cardiac involvement (e.g., myocarditis, cardiomyopathy), renal impairment, peripheral neuropathy, and pulmonary fibrosis.
Research & developmentsStudies are ongoing regarding new biologics, targeted therapies, and personalized approaches to treatment.
BiomarkersANCA, eosinophil counts, IgE levels, and biomarkers are being evaluated to contribute to diagnosis and monitoring.
Prognostic factorsInvolvement of the heart, renal impairment, and higher eosinophil counts are related to worse outcomes.

ESR: erythrocyte sedimentation rate; CRP: C-reactive protein.