Journal of Neurology Research, ISSN 1923-2845 print, 1923-2853 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Neurol Res and Elmer Press Inc
Journal website https://jnr.elmerpub.com

Case Report

Volume 000, Number 000, October 2026, pages 000-000


Eosinophilic Granulomatosis With Polyangiitis Misdiagnosed as Hyper-Eosinophilic Syndrome: A Case Report

Tables

↓  Table 1. Hematological Biochemical Profile of Patient
 
InvestigationPatient resultNormal range
ESR: erythrocyte sedimentation rate; SGPT: serum glutamic pyruvic transaminase; RBS: random blood glucose; CRP: C-reactive protein.
Hemoglobin13 g/dL13–17 g/dL
Platelets650,000/mm3150,000–450,000/mm3
Total leucocytes27,310/mm34,000–10,000/mm3
Neutrophils19.9%40–80%
Lymphocytes10.9%20–40%
Eosinophils65.1%1–6%
Absolute eosinophil count17.8 × 109/L< 0.5 × 109/L
Monocytes3.5%2–10%
Basophils0.6%< 1%
Reticulocyte count1%0.5–2%
ESR60 mm/1st h0–15 mm/1st h
Serum creatinine0.7 mg/dL0.6–1.2 mg/dL
Sodium140 mmol/L135–150 mmol/L
Potassium3.77 mmol/L3.5–5.1 mmol/L
Chloride106 mmol/L96–112 mmol/L
Serum bilirubin0.3 mg/dL0.1–1.0 mg/dL
SGPT11 U/L10–50 U/L
Alkaline phosphatase102 U/L40–129 U/L
RBS82 mg/dL70–140 mg/dL
CRP< 0.4 mg/dL< 1.0 mg/dL

 

↓  Table 2. Investigations for Secondary Causes of Eosinophilia and Organ Involvement
 
Investigation categoryInvestigationPatient finding
COVID-19: coronavirus disease 2019; HBsAg: hepatitis B virus antigen; HCV: hepatitis C virus; HIV: human immunodeficiency virus; p-ANCA/MPO-ANCA: perinuclear-staining antineutrophil cytoplasmic antibody/myeloperoxidase-antineutrophil cytoplasmic antibody; ECG: electrocardiogram; NT-proBNP: N-terminal pro-brain natriuretic peptide; LVEF: left ventricular ejection fraction.
Infectious and parasitic evaluationStool routine examinationNormal
Stool ova and parasites examination (three serial samples)Negative for helminthic ova, protozoal cysts, and rhabditiform larvae
Thick and thin blood filmNegative for Plasmodium species and microfilariae
Blood cultureNo growth
Urine cultureNo growth
COVID-19 antigenNegative
HBsAgNon-reactive
Anti-HCVNon-reactive
HIVNegative
Autoimmune and systemic evaluationAntinuclear antibodyNegative
p-ANCA/MPO-ANCAPositive (100 AU)
UrinalysisNormal; no proteinuria, pus cells, or casts
Ultrasound abdomen and pelvisNormal
Cardiac evaluation12-lead ECGNormal sinus rhythm; no significant ST-T or conduction abnormalities
Transthoracic echocardiographyLVEF 62%; no regional wall-motion abnormality, intracardiac thrombus, apical obliteration, or pericardial effusion
High-sensitivity troponin I4.8 ng/L (normal < 14 ng/L)
NT-proBNP68 pg/mL (normal < 125 pg/mL)

 

↓  Table 3. The 2022 ACR/EULAR Classification Criteria for Eosinophilic Granulomatosis With Polyangiitis
 
Criterion categoryCriterion itemWeight (points)Patient presentationPoints assigned
Classification rule: After exclusion of mimics of vasculitis and in a patient with an established diagnosis of small- or medium-vessel vasculitis, a cumulative score ≥ 6 supports classification as EGPA. Sensitivity: 85%, specificity: 99%. ACR/EULAR: American College of Rheumatology and European Alliance of Associations for Rheumatology; ANCA: antineutrophil cytoplasmic antibody; EGPA: eosinophilic granulomatosis with polyangiitis.
Clinical criteriaObstructive airway disease (e.g., asthma)+3Documented adult-onset asthma+3
Nasal polyps+3Not documented0
Mono-neuritis multiplex or motor neuropathy (not due to radiculopathy)+1Severe motor-predominant axonal polyneuropathy; bilateral foot drop+1
Laboratory and biopsy criteriaBlood eosinophil count ≥ 1 × 109/L+5Peak eosinophils: 17.8 × 109/L (65.1% of 27,310/µL)+5
Extravascular eosinophilic-predominant inflammation on biopsy+2Not performed (skin/nerve biopsy not performed)0
Cytoplasmic ANCA or anti-proteinase 3 (PR3)-ANCA positivity−3PR3-ANCA negative0
Hematuria−1Absent; urinalysis normal0
Total score+9