努南综合征及相关疾病的恶性疾病。

Hormone research Pub Date : 2009-12-01 Epub Date: 2009-12-22 DOI:10.1159/000243773
Henrik Hasle
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引用次数: 63

摘要

患有Noonan综合征、心-面-皮综合征、Costello综合征或LEOPARD综合征的儿童患癌症的总体风险很高,尽管没有准确的估计。关于成人NS患者的癌症数据很少,但报道的成人恶性肿瘤的数量似乎并不多。少年型髓细胞白血病(JMML)是一种罕见的侵袭性白血病。在大约30名患有NS和PTPN11突变的新生儿中描述了一种jmml样骨髓增生性疾病。这种疾病通常会自行消退,但也可能出现致命的并发症。文献综述表明,NS患者急性淋巴细胞白血病和急性髓性白血病的风险增加。患有科斯特洛综合征的幼儿患横纹肌肉瘤的风险极高,患神经母细胞瘤和膀胱癌的风险也增加。有必要对分子遗传学诊断的NS及相关疾病患者进行登记研究,并进行高质量的长期随访,以进一步估计恶性肿瘤的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malignant diseases in Noonan syndrome and related disorders.

The overall risk of cancer in children with Noonan (NS), cardio-facial-cutaneous, Costello or LEOPARD syndrome is high, although no precise estimates are available. There are few data on cancer in adults with NS, but the reported numbers of malignancies in adults do not seem excessive. Juvenile myelomonocytic leukemia (JMML) is a rare aggressive leukemia in young children. A JMML-like myeloproliferative disorder has been described in about 30 neonates with NS and the PTPN11 mutation. The disorder often regresses spontaneously, but fatal complications may occur. A review of the literature indicates an increased risk of acute lymphoblastic leukemia and acute myeloid leukemia in NS. Young children with Costello syndrome have an extremely high risk of rhabdomyosarcoma, and also an increased risk of neuroblastoma and bladder carcinoma. Registry-based studies of patients with NS and related disorders diagnosed with molecular genetics and a high-quality long-term follow-up are necessary to further estimate the incidence of malignancy.

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Hormone research
Hormone research 医学-内分泌学与代谢
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