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A Case of Effective Mepolizumab Induction Therapy for Severe Eosinophilic Granulomatosis with Polyangiitis Diagnosed by Eosinophilic Cholecystitis and Interstitial Nephritis
Author(s) -
Keita Hattori,
Yuri Teramachi,
Yoshinori Kobayashi,
Takeshi Ito,
Takatoshi Morinaga,
Hirohumi Tamai,
Yoshihiro Yamamoto
Publication year - 2021
Publication title -
case reports in rheumatology
Language(s) - English
Resource type - Journals
eISSN - 2090-6889
pISSN - 2090-6897
DOI - 10.1155/2021/6678893
Subject(s) - mepolizumab , granulomatosis with polyangiitis , medicine , eosinophilic , pathology , eosinophilic pneumonia , eosinophil , eosinophilia , sinusitis , asthma , vasculitis , gastroenterology , immunology , respiratory disease , disease , lung
A 66-year-old man with a history of bronchial asthma and sinusitis was admitted with cholecystitis and peripheral neuropathy. The histopathological findings of the gallbladder revealed necrotic vasculitis and granulomatous inflammation with marked eosinophilic infiltration. Kidney biopsy also showed marked eosinophilic infiltration in the tubulointerstitial area and eosinophilic tubulitis. He was diagnosed with eosinophilic granulomatosis with polyangiitis (EGPA) and treated with corticosteroids. However, he showed no response. Therefore, he was administered mepolizumab 300 mg, which resulted in clinical improvement, including normalization of the eosinophil and CRP levels. We herein describe the first case of successful induction therapy of EGPA using mepolizumab.

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