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DOI 10.1159/000516255

Медицинская библиотека · Case reports in neurology · 2021

Eosinophilic Granulomatosis with Polyangiitis Presenting with Myocarditis as an Initial Symptom: A Case Report and Review of the Literature.

Kurihara Kanako, Tsugawa Jun, Ouma Shinji, Ogata Toshiyasu, Aoki Mikiko, Omoto Masatoshi, Kanda Takashi, Tsuboi Yoshio

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Аннотация

A 66-year-old woman with a history of bronchial asthma had shortness of breath and fatigue upon mild exercise. She was diagnosed as congestive heart failure. A blood test showed eosinophilia without the presence of anti-neutrophil cytoplasmic antibody (ANCA), and a myocardial biopsy specimen revealed eosinophilic infiltration in the myocardium. Eosinophilia was improved when she was administered short-term methylprednisolone. After that, she had numbness and pain in her lower limbs with re-elevation of eosinophils. She had dysesthesia and hypalgesia in the distal part of the limbs. Sural nerve biopsy revealed axonal degeneration and thickness of the arterial wall, indicating a diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA). Two courses of steroid pulse therapy were performed, resulting in marked improvement of her sensory symptoms. ANCA-negative EGPA might be associated with myocarditis and peripheral neuropathy. A sufficient immunotherapy should have been considered to prevent rapid progression.

Для цитирования: Kurihara Kanako, Tsugawa Jun, Ouma Shinji, Ogata Toshiyasu, Aoki Mikiko, Omoto Masatoshi, Kanda Takashi, Tsuboi Yoshio. Eosinophilic Granulomatosis with Polyangiitis Presenting with Myocarditis as an Initial Symptom: A Case Report and Review of the Literature.. Case reports in neurology. 2021. DOI: 10.1159/000516255.
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