[
    {
        "id": "osp-2146",
        "type": "article-journal",
        "title": "Cutaneous Vasculitis as Early Presentation of Eosinophilic Granulomatosis with Polyangiitis without Systemic Symptoms",
        "author": [
            {
                "family": "Sulaiman",
                "given": "Wahinuddin"
            },
            {
                "family": "Abdullah",
                "given": "Aris Chandran"
            },
            {
                "family": "Chung",
                "given": "Sin Fah"
            },
            {
                "family": "Karim",
                "given": "Norain"
            },
            {
                "family": "Tang",
                "given": "Jyi Jong"
            }
        ],
        "URL": "https://omanscience.com/en/articles/cutaneous-vasculitis-as-early-presentation-of-eosinophilic-granulomatosis-with-polyangiitis-without-systemic-symptoms",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2019
                ]
            ]
        },
        "container-title": "Oman Medical Journal",
        "DOI": "10.5001/omj.2019.67",
        "publisher": "Oman Medical Specialty Board",
        "ISSN": "1999-768X",
        "abstract": "Eosinophilic granulomatosis with polyangiitis (formerly known as Churg-Strauss syndrome) is a rare vasculitis in children. It commonly presents with respiratory symptoms, especially asthma, allergic rhinitis, and peripheral eosinophilia. Involvement of other systems, such as renal and cardiac, may carry a poor prognosis. Anti-neutrophil cytoplasmic antibodies have been found less frequently in children with this condition. We report a case of a 15-year-old male who presented with indurated and pruritic papules on both legs and peripheral eosinophilia without other system involvement. Histopathological findings from a skin biopsy were suggestive of eosinophilic granulomatosis with polyangiitis. Anti-neutrophil cytoplasmic antibodies were negative."
    }
]