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先天性纯红细胞再生障碍性贫血:一家三级医疗中心的诊治经验。

Diamond blackfan anemia: a tertiary care center experience.

机构信息

Department of Hematology, All India Institute of Medical Science, New Delhi, India.

出版信息

Mediterr J Hematol Infect Dis. 2013 Jun 3;5(1):e2013039. doi: 10.4084/MJHID.2013.039. Print 2013.

Abstract

Diamond Blackfan Anemia (DBA) is a rare hypoplastic anemia that presents in infancy with macrocytic anemia and reticulocytopenia. It is a ribosomopathy with autosomal dominant inheritance. In our series of 10 patients with DBA, congenital malformations were observed in 50% of the cases. Age at symptom onset ranged from 0-12 months. Age at diagnosis ranged from 4 months to 96 months. Male: female ratio was 9:1. Response to prednisolone was observed in 4 out of the 10 patients (either during initial treatment or during re-challenge). Response to cyclosporine was found to be poor. Bone marrow transplantation was successful in attaining remission in one patient. Malignancies were not reported in any patient possibly due to a short follow up period.

摘要

先天性红细胞生成性卟啉病(DBA)是一种罕见的再生障碍性贫血,在婴儿期表现为巨幼细胞性贫血和网织红细胞减少症。它是一种常染色体显性遗传的核糖体病。在我们的 10 例 DBA 患者系列中,50%的病例观察到先天性畸形。症状发作的年龄从 0-12 个月不等。诊断时的年龄从 4 个月到 96 个月不等。男女比例为 9:1。10 例患者中有 4 例(无论是在初始治疗期间还是在重新治疗期间)对泼尼松有反应。环孢素反应不佳。骨髓移植在 1 例患者中成功缓解。由于随访时间短,任何患者均未报告恶性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ece/3684352/e38851c04f82/mjhid-5-1-e2013039f1.jpg

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