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Primary immunodeficiencies and haemato-oncology
被引:0
|作者:
Muller Judit
[1
]
Kovacs Gabor
[1
]
机构:
[1] Semmelweis Egyet, Altalanos Orvostudomanyi Kar, Gyermekgyogyaszati Klin 2, Budapest, Hungary
关键词:
primary immunodeficiency;
malignancy;
lymphoma;
chromosomal breakage;
WISKOTT-ALDRICH-SYNDROME;
LINKED LYMPHOPROLIFERATIVE DISEASE;
ATAXIA-TELANGIECTASIA;
PEDIATRIC-PATIENTS;
INCREASED RISK;
BREAST-CANCER;
DISORDERS;
MALIGNANCIES;
DEFICIENCY;
LYMPHOMA;
D O I:
10.1556/650.2018.31240
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Primary immunodeficiencies (PID) are rare, congenital disorders, often associated with genetic defects in the immune system. According to our current knowlegde, about 350 genes are involved in distinct immunodeficiency disorders. In PIDs at least one, and often more, immune component is impaired, missing, or has an inappropriate function. The prevalence of PID has been increasing. Due to advances in the treatment of PID, especially immunoglobulin replacement therapy and stem cell transplantation, the life expectancy of patients is longer. As patients with PID live longer, malignancies are diagnosed more commonly. Patients with PID are at an increased risk of malignancy compared with the normal population. Malignancy is the second most common cause of death in these patients after infections. The aim of this article is to review the malignancies and their clinical relevance in patients with PID.
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页码:2073 / 2078
页数:6
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