MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1002/ajh.2830450407

Медицинская библиотека · American journal of hematology · 1994

Thrombotic microangiopathy and retroviral infections: a 13-year experience.

Ucar A, Fernandez H F, Byrnes J J, Lian E C, Harrington W J

Клинический случайСтатьяПеревод в очереди

Аннотация

Eleven of fifty serum samples collected from patients with a diagnosis of thrombotic microangiopathy (TMA), from 1979 to 1991, tested positive for antiretroviral antibodies. Seven had human immunodeficiency virus (HIV) infection, and four had human lymphotrophic virus, type I (HTLV-I) infection. All patients were treated with plasma exchange and/or infusion, but only two of the HIV-infected patients obtained a complete response (CR) and one of them died after a few months. Combined results from the literature indicate that most patients with HIV infection survive less than one year from the initial diagnosis of TMA. In the setting of HIV infection, TMA is a treatable condition, but survival for most patients is less than 12 months. Three of the four HTLV-I infected patients with TMA had a CR. These observations strongly suggest that both HIV and HTLV-I infections are associated with TMA, but rigorous epidemiologic studies will be needed to determine the relative risk for each. Retroviral infections should be considered in patients with TMA, especially if the patient has associated risk factors and demographic characteristics.

Для цитирования: Ucar A, Fernandez H F, Byrnes J J, Lian E C, Harrington W J. Thrombotic microangiopathy and retroviral infections: a 13-year experience.. American journal of hematology. 1994. DOI: 10.1002/ajh.2830450407.

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.