Management of Generalized Body Ache with Elevated CRP and Eosinophilia
This patient requires immediate evaluation for parasitic infection with empirical treatment of albendazole 400 mg plus ivermectin 200 μg/kg if travel history to endemic regions exists, while simultaneously ruling out serious systemic conditions including eosinophilic granulomatosis with polyangiitis (EGPA) and hypereosinophilic syndrome (HES). 1
Initial Diagnostic Approach
Essential Travel and Exposure History
- Document detailed travel history to tropical/subtropical regions, particularly Southeast Asia, Africa, Central/South America, or Eastern Europe, as parasitic infections are the most common cause of eosinophilia in returning travelers 2
- Inquire about consumption of raw or undercooked meat (particularly pork), fish, snails, prawns, crabs, or frogs 2
- Ask about freshwater exposure (swimming, wading) for schistosomiasis risk 2
Critical Laboratory Investigations
- Complete blood count with differential to quantify absolute eosinophil count (this patient has 1.0 × 10⁹/L, which meets the threshold for hypereosinophilia) 2, 1
- Stool studies: concentrated stool microscopy (minimum 3 samples) and PCR for parasites 2, 1
- Serology for parasites: Strongyloides, Schistosoma, Toxocara, Trichinella (available through specialized tropical disease centers) 2
- ANCA testing (both MPO-ANCA and PR3-ANCA) to evaluate for EGPA, as 30-40% of EGPA patients are ANCA-positive 2
- Urinalysis for hematuria and proteinuria to assess for glomerulonephritis 2, 3
- Creatine kinase level (elevated in trichinellosis and some vasculitides) 2
Assess for End-Organ Involvement
The presence of eosinophilia with systemic symptoms mandates evaluation for organ damage:
Cardiac assessment (highest priority for morbidity/mortality):
- ECG and echocardiogram to evaluate for eosinophilic cardiomyopathy, which can occur in HES, EGPA, and trichinellosis 2
Pulmonary evaluation:
- Chest imaging (CT preferred) for infiltrates, nodules, or pleural effusion 2, 3
- Consider pulmonary function tests if respiratory symptoms present 3
Neurological examination:
- Assess for peripheral neuropathy (mononeuritis multiplex is characteristic of EGPA) 2
- If CNS symptoms present, obtain MRI brain/spine and consider lumbar puncture with specific request for eosinophil count in CSF 2
Other systems:
- Skin examination for purpura, nodules, or urticarial rash 2
- Assess for rhinosinusitis symptoms or nasal polyps (suggestive of EGPA) 2
Treatment Algorithm
If Travel History to Endemic Regions Present:
Empirical antiparasitic therapy is recommended as first-line treatment while awaiting diagnostic results, as parasitic infections are the most common reversible cause and delayed treatment can lead to complications 1:
- Albendazole 400 mg single dose PLUS ivermectin 200 μg/kg single dose 1
- This combination covers the most common helminthic infections including strongyloidiasis, hookworm, and other soil-transmitted helminths 2, 1
Important caveat: If strongyloidiasis is suspected or confirmed, do NOT initiate corticosteroids before treating with ivermectin, as steroids can cause fatal hyperinfection syndrome 2
If Specific Parasites Identified:
- Schistosomiasis: Praziquantel 40 mg/kg in divided doses for 1-3 days 2, 1
- Trichinellosis (if severe myalgia, periorbital edema, very high eosinophils >3 × 10⁹/L): Albendazole 400 mg daily for extended course 2
- Liver flukes: Praziquantel 25 mg/kg three times daily for 2-3 days 2
If No Travel History or Parasitic Workup Negative:
Evaluate for EGPA if the following features are present:
- Asthma or chronic rhinosinusitis 2
- Peripheral neuropathy 2
- Lung infiltrates 2
- Palpable purpura or other skin lesions 2
ACR-EULAR 2022 criteria (score ≥6 suggests EGPA in context of small/medium vessel vasculitis):
- Eosinophil count ≥1 × 10⁹/L: +5 points 2
- Obstructive airway disease: +3 points 2
- Nasal polyps: +3 points 2
- Mononeuritis multiplex/motor neuropathy: +1 point 2
Treatment for EGPA with organ-threatening manifestations:
- Glucocorticoids (prednisone 1 mg/kg/day, typically 40-60 mg daily) as initial therapy 2, 4
- Add cyclophosphamide or rituximab for severe disease with renal insufficiency, cardiomyopathy, GI involvement, or CNS involvement 2
If Idiopathic Hypereosinophilic Syndrome (HES) Suspected:
HES is a diagnosis of exclusion requiring:
- Sustained eosinophilia ≥1.5 × 10⁹/L for at least 6 months 5, 6
- Evidence of end-organ damage 5, 6, 7
- Exclusion of secondary causes and clonal eosinophilia 5, 6, 7
Molecular testing is critical:
- Test for PDGFRA, PDGFRB, or FGFR1 rearrangements, as these predict response to imatinib 5, 6, 7
- If fusion-positive: Imatinib is the treatment of choice with dramatic responses 6, 7
- If fusion-negative: Prednisone 1 mg/kg/day is first-line therapy 5, 6, 7
Symptomatic Management:
While awaiting definitive diagnosis:
- Topical emollients and antihistamines for pruritus 1
- Avoid corticosteroids until strongyloidiasis is definitively excluded 2
- Monitor closely for development of organ involvement, particularly cardiac complications 2, 6
Critical Pitfalls to Avoid
- Never start corticosteroids before excluding or treating strongyloidiasis in anyone with potential exposure, as this can cause fatal disseminated infection 2
- Do not rely on single stool sample - sensitivity is poor; obtain at least 3 concentrated specimens 2
- Do not dismiss normal ANCA - 60-70% of EGPA patients are ANCA-negative, particularly those with cardiac involvement 2
- Do not delay cardiac evaluation - eosinophilic cardiomyopathy can be rapidly progressive and life-threatening 2, 6
- Do not assume symptoms correlate with disease activity - significant organ damage can occur with minimal symptoms 8, 6
Follow-Up Strategy
- Repeat eosinophil count in 2-4 weeks after empirical antiparasitic therapy 1
- If eosinophilia persists despite treatment, proceed with comprehensive evaluation for primary eosinophilic disorders 5, 6, 7
- Serial cardiac monitoring if eosinophilia remains elevated, as cardiac involvement can develop insidiously 6, 7