[
    {
        "id": "osp-2749",
        "type": "article-journal",
        "title": "Bullous Pyoderma Gangrenosum Associated with Antiphospholipid Syndrome: A Case Report and Literature Review",
        "author": [
            {
                "family": "Alwashahi",
                "given": "Yousuf"
            },
            {
                "family": "Al-Bahrani",
                "given": "Mayar"
            },
            {
                "family": "Almoqbali",
                "given": "Ahmed"
            },
            {
                "family": "Alajmi",
                "given": "Asma"
            }
        ],
        "URL": "https://omanscience.com/en/articles/bullous-pyoderma-gangrenosum-associated-with-antiphospholipid-syndrome-a-case-report-and-literature-review",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2024
                ]
            ]
        },
        "container-title": "Oman Medical Journal",
        "DOI": "10.5001/omj.2024.26",
        "publisher": "Oman Medical Specialty Board",
        "ISSN": "1999-768X",
        "abstract": "We report a rare case of a middle-aged Omani woman who was known to have primary antiphospholipid syndrome, glucose-6-phosphate dehydrogenase deficiency, and iron deficiency anemia. Cannulation attempts caused bulla which progressed to ulceration. A pathergy phenomenon with high suspicion of pyoderma gangrenosum was postulated. Management with corticosteroids, cyclosporin, and finally ustekinumab, a novel biologic agent, yielded a beneficial response."
    }
]