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努南综合征及相关疾病中的恶性疾病。

Malignant diseases in Noonan syndrome and related disorders.

作者信息

Hasle Henrik

机构信息

Department of Pediatrics, Aarhus University Hospital Skejby, Denmark.

出版信息

Horm Res. 2009 Dec;72 Suppl 2:8-14. doi: 10.1159/000243773. Epub 2009 Dec 22.

Abstract

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.

摘要

努南综合征(NS)、心面皮肤综合征、科斯特洛综合征或豹皮综合征患儿患癌的总体风险很高,尽管尚无确切估计数据。关于成年NS患者患癌的数据很少,但报告的成年恶性肿瘤病例数似乎并不过多。青少年粒单核细胞白血病(JMML)是幼儿中一种罕见的侵袭性白血病。在约30例患有NS和PTPN11突变的新生儿中,曾描述过一种类似JMML的骨髓增殖性疾病。这种疾病通常会自发缓解,但可能会发生致命并发症。文献综述表明,NS患者患急性淋巴细胞白血病和急性髓系白血病的风险增加。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。有必要对通过分子遗传学诊断的NS及相关疾病患者进行基于登记的研究,并进行高质量的长期随访,以进一步估计恶性肿瘤的发病率。

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