Hepatic Lesions With Eosinophilic Granulomatosis With Polyangiitis

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Authors: Miyu Wakatsuki, Hiroyuki Yamashita, Hiroshi Kaneko
Cited by: 0
References: 8

Abstract

The data that support the findings of this study are available from the corresponding author upon reasonable request. Figure S1: Clinical course of each patient (A; case 1, B; case 2, respectively). Figure S2: Skin biopsy of Case 2. The vascular walls exhibit fibrinoid necrotic degeneration, indicative of fibrinoid vasculitis (A). Extensive eosinophilic infiltration is present throughout the subcutaneous tissue (B). Table S1: Laboratory data from the time of admission. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Fields of Study & Subjects

Vasculitis and related conditions Eosinophilic Disorders and Syndromes Autoimmune and Inflammatory Disorders

Publication details

Journal / source
International Journal of Rheumatic Diseases
Volume
29
Issue
3
Pages
e70583–e70583
Publication date
1 March 2026
Language
EN