3.8 Article

A rare case of combined immunodeficiency with cytopenia whose symptoms were controlled by cyclosporine

期刊

OXFORD MEDICAL CASE REPORTS
卷 2022, 期 5, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/omcr/omac055

关键词

-

向作者/读者索取更多资源

Combined Immunodeficiency (CID) is a group of inborn error of Immunity (IEI) that can result in infectious and non-infectious complications. This case report highlights the potential beneficial role of cyclosporine in controlling cytopenia in CID patients.
Combined Immunodeficiency (CID) is a group of inborn error of Immunity (IEI) that may present with both infectious and non-infectious complications. Autoimmunity is an unusual presentation of CID and can be presented as cytopenia. The initial management of cytopenia is corticosteroids and IVIG. The role of other cytotoxic and immunosuppressive drugs in management of cytopenia is not fully understood. The objective of this clinical case report is to highlight the possibly beneficial role of cyclosporine in controlling cytopenia in CID patients. A 26-month-old child with generalized ecchymosis was referred to Mofid Children's Hospital in Tehran, Iran. Physical examination revealed no substantial findings other than ecchymosis, and complete blood count (CBC) revealed thrombocytopenia. Diagnosis of CID and cytopenia followed. The patient was treated by 5 times prednisolone and 4 times Rituximab. Finally, his ecchymosis was controlled by Cellcept, which was then tempered and substituted by cyclosporine.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据