Medicine · Rheumatology (SLE, RA, Vasculitis, Crystal Arthropathies, Scleroderma)

A 36-year-old woman with adult-onset asthma and chronic nasal congestion presents with a right foot drop and patchy sensory loss in the left arm. Total leucocyte count is 19,000/uL with 32% mature eosinophils. Chest CT shows fleeting migratory infiltrates. ANCA testing by ELISA shows antimyeloperoxidase specificity. Cardiac function is normal. What is the most likely diagnosis?

  • A Eosinophilic granulomatosis with polyangiitis (Churg-Strauss)
  • B Granulomatosis with polyangiitis
  • C Microscopic polyangiitis
  • D Hypereosinophilic syndrome with neuropathy
Correct answer: A. Eosinophilic granulomatosis with polyangiitis (Churg-Strauss)

Explanation

The triad of asthma and allergic rhinitis, marked peripheral blood eosinophilia, and vasculitic neuropathy defines eosinophilic granulomatosis with polyangiitis. Roughly 40% of patients are MPO-ANCA positive; those who are ANCA positive tend toward small-vessel vasculitic manifestations such as neuropathy and glomerulonephritis. GPA typically causes granulomatous sinus disease and cavitating lung lesions without eosinophilia, while hypereosinophilic syndrome causes endomyocardial fibrosis rather than vasculitis.

Reference: Harrison's Principles of Internal Medicine, 21st ed.

High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP

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