医学
突变
恶性肿瘤
髓系白血病
白血病
癌症研究
造血干细胞移植
PTPN11型
移植
癌症
免疫学
基因
遗传学
病理
内科学
生物
结直肠癌
克拉斯
作者
Nihan Bayram,Yöntem Yaman,Murat Elli,Kürşat Özdilli,Serdar Nepesov,Mehmet Sait Doğan,Akif Ayaz,Sema Anak
摘要
BACKGROUND: PNPK gene mutations result in DNA repair disorders and have a spectrum of neurodevelopmental manifestations. To date, cancer predisposition has not been described in patients with PNKP mutations. OBSERVATION: Here, we report a patient with PNKP mutation, who developed AML at age of five and underwent reduced-intensity HSCT. CONCLUSION: Although many DNA repair disorders are known to have increased risk of malignancy, association between PNKP mutations and malignancy is not well-described. This report is the first description of a PNPK mutation patient developing a malignancy and undergoing curative HSCT.
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