MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1097/iop.0000000000001849

Медицинская библиотека · Ophthalmic plastic and reconstructive surgery · 2021

Bilateral Nodular Episcleritis: A Rare Presentation of Relapsing Polychondritis.

Meel Rachna, Das Deepsekhar, Bhadu Danveer, Sen Seema, Kishor Kriti, Pushker Neelam

Клинический случайСтатьяПеревод в очереди

Аннотация

Herein, the authors report a case of relapsing polychondritis (RP) presenting as isolated bilateral nodular episcleritis. A 23-year-old male presented to us with bilateral large ocular surface masses for which he had received antitubercular medications. A workup was performed to rule out infective, neoplastic, and immune etiologies, after which the patient was then treated empirically with systemic steroids. No response to steroids was noted, so the lesions were removed surgically. On follow up, he developed redness of both ears sparing the lobules. A biopsy from ear lesions supported the diagnosis of RP. At a follow up of 2 years, the patient is free of any ocular or systemic manifestation. To the best of the authors' knowledge, this is the first reported case of RP presenting with bilateral giant nodular episcleritis and treated successfully with surgery. A multidisciplinary approach is essential for the management of such cases. A long-term close follow up is vital for early detection of associated malignancies like multiple myeloma.

Для цитирования: Meel Rachna, Das Deepsekhar, Bhadu Danveer, Sen Seema, Kishor Kriti, Pushker Neelam. Bilateral Nodular Episcleritis: A Rare Presentation of Relapsing Polychondritis.. Ophthalmic plastic and reconstructive surgery. 2021. DOI: 10.1097/iop.0000000000001849.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.