An Adolescent with Recurrent Intracranial Hemorrhage, and Skin Lesion

We presented an adolescent with recurrent intracranial hemorrhage and skin lesion. The diagnosis was unclear and the treatment was difficult. Through a multidisciplinary effort type Ⅰ interferon disease was suspected and later, an interferon-stimulated gene was further detected. Considering the high...

Бүрэн тодорхойлолт

Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид: HONG Yuehui, SHEN Min, WANG Tao, MA Mingsheng, ZHAO Sen, FENG Feng, ZHAO Dachun, ZHANG Wen, ZENG Xuejun, XUAN Lei, YAO Ming, ZHU Yicheng
Формат: Өгүүллэг
Хэл сонгох:zho
Хэвлэсэн: Editorial Office of Journal of Rare Diseases 2022-04-01
Цуврал:罕见病研究
Нөхцлүүд:
Онлайн хандалт:https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2022.02.009
Тодорхойлолт
Тойм:We presented an adolescent with recurrent intracranial hemorrhage and skin lesion. The diagnosis was unclear and the treatment was difficult. Through a multidisciplinary effort type Ⅰ interferon disease was suspected and later, an interferon-stimulated gene was further detected. Considering the high morbidity and fatality rate of recurrent intracranial hemorrhage, tofacitinib and hydroxychloroquine were administered. After treatment, the livedo reticularis was significantly regressed. Unfortunately, the intracranial hemorrhage recurred due to a pre-existing cerebral aneurysm, leading to death of the patient. The diagnosis and treatment of this case highlight the importance of multidisciplinary collaboration in the diagnosis and treatment of difficult and rare diseases.
ISSN:2097-0501