What is the diagnostic approach for eosinophilia gastropathy?

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Last updated: December 20, 2025View editorial policy

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Diagnostic Approach for Eosinophilic Gastropathy

Eosinophilic gastropathy requires upper endoscopy with multiple gastric and duodenal biopsies showing ≥20 eosinophils per high-power field (0.3 mm²), combined with compatible clinical symptoms and exclusion of secondary causes of eosinophilia. 1, 2

Clinical Presentation to Recognize

Adults typically present with:

  • Abdominal pain, nausea, and vomiting 3, 2
  • Symptoms may occur without any history of allergic reactions 3

Children present with age-dependent symptoms:

  • Younger children: feeding difficulties, failure to thrive, vomiting, diarrhea 4
  • Older children: abdominal pain and dysphagia 4

Laboratory Testing Strategy

Order these specific tests:

  • Complete blood count with differential to assess peripheral eosinophilia (≥500 eos/µL increases diagnostic probability significantly) 2, 5
  • Serum albumin level (hypoalbuminemia <3.5 g/dL increases diagnostic yield) 5
  • The combination of peripheral eosinophilia AND hypoalbuminemia increases biopsy diagnostic yield to 25% 5

Critical caveat: Normal peripheral eosinophil counts do NOT exclude the diagnosis—tissue eosinophilia can occur with normal blood counts 3, 2

Endoscopic Approach

Proceed with upper endoscopy even if mucosa appears grossly normal:

  • Endoscopic appearance is frequently normal and unreliable for diagnosis 3, 5
  • Ultrasound or CT may show thickened intestinal walls and ascites before endoscopic changes appear 3

Biopsy protocol (this is essential):

  • Obtain biopsies from BOTH stomach and duodenum regardless of endoscopic appearance 1, 5
  • Take multiple biopsies from different anatomical sites to account for patchy distribution 1, 6
  • Include both targeted biopsies (from any visible abnormalities) and random biopsies 3
  • In pediatric patients, biopsy all patients undergoing endoscopy for GI symptoms, as appearance is particularly unreliable 4, 5

Histopathologic Diagnostic Criteria

The definitive diagnosis requires:

  • ≥20 eosinophils per high-power field (0.3 mm²) in gastric and/or duodenal mucosa 1, 2
  • Additional supportive histologic features: eosinophil microabscesses, degranulation, surface layering 1
  • Count eosinophils in the most densely infiltrated area (peak count) 1

Important pitfall: If initial biopsies are negative but clinical suspicion remains high, obtain ascitic fluid for cytology if present, and repeat endoscopy with more extensive multisite sampling 3

Exclusion of Secondary Causes

Must rule out these conditions before confirming diagnosis:

  • Parasitic infections (obtain stool studies for ova and parasites) 2, 6
  • Drug hypersensitivity reactions 6
  • Inflammatory bowel disease 6
  • Connective tissue disorders 6
  • Malignancy 6

Diagnostic Algorithm Summary

  1. High clinical suspicion if patient presents with chronic abdominal pain, nausea, vomiting, or diarrhea 3, 2
  2. Check CBC with differential and serum albumin - if peripheral eosinophilia (≥500 eos/µL) and/or hypoalbuminemia (<3.5 g/dL) present, diagnostic yield increases substantially 5
  3. Perform upper endoscopy with multiple biopsies from stomach and duodenum regardless of mucosal appearance 1, 5
  4. Confirm histologically with ≥20 eosinophils/HPF 1, 2
  5. Exclude secondary causes through appropriate testing 6
  6. If negative but suspicion high: obtain ascitic fluid if present, repeat endoscopy with more extensive sampling 3

The diagnostic yield increases from 1.2% overall to 7.7% with peripheral eosinophilia alone, 9.1% with hypoalbuminemia alone, and 25% when both are present. 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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