MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1097/mph.0000000000001985

Медицинская библиотека · Journal of pediatric hematology/oncology · 2021

Autoimmune Liver Disease in Patients With Sickle Cell Disease.

Waisbourd-Zinman Orith, Frenklak Rachel, Hakakian Odelia, Hilmara Didja, Lin Henry

СтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

Hepatic and biliary tract diseases are common in sickle cell disease (SCD) patients, likely due to sickling, hemosiderosis, viral hepatitis, or cholelithiasis. Literature is lacking on associations between SCD, autoimmune hepatitis (AIH), and/or sclerosing cholangitis (SC)-together, autoimmune liver disease (AILD). We aimed to better understand the relationship of these diseases in pediatric patients.

MATERIALS AND

METHODS

A retrospective analysis of patients with SCD and AILD at the Children's Hospital of Philadelphia (January 2008 to August 2015).

RESULTS

Seven patients, ages 8 to 23 years (3 males), were identified. Three had AIH, 2 SC, and 2 AIH/SC overlap, known as autoimmune SC. All patients with AIH treated with azathioprine significantly improved their liver enzymes. One patient with SC and inflammatory bowel disease underwent successful bone marrow transplant. Two SC patients died from SCD complications.

CONCLUSIONS

In this cohort, there seems to be an association between SCD and AILD; SC in this population was severe. Physicians should be aware of this and evaluate patients with SCD and elevated liver enzymes for AILD.

Для цитирования: Waisbourd-Zinman Orith, Frenklak Rachel, Hakakian Odelia, Hilmara Didja, Lin Henry. Autoimmune Liver Disease in Patients With Sickle Cell Disease.. Journal of pediatric hematology/oncology. 2021. DOI: 10.1097/mph.0000000000001985.

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.