Mutafoğlu-Uysal Kamer, Günes Dilek, Tüfekçi Ozlem, Kalelihan-Cankal Aydan, Sarialioğlu Faik, Olgun Nur
Department of Pediatric Oncology, Institute of Oncology, Izmir, Turkey.
Turk J Pediatr. 2009 Sep-Oct;51(5):444-52.
We evaluated the incidence of congenital malformations in 566 children (median age: 8, M:F 1.3) with lymphomas and solid tumors using patient records. In this study, 12.7% of children either had a congenital malformation (7.8%) or a birthmark (4.9%). The incidence of patients with a childhood cancer syndrome was 3% and these cases developed typical tumors. The rate of consanguineous marriages was 12.6%, and family history of cancer was positive in 31.2%. Median age at cancer diagnosis, gender, maternal age, history of stillbirth and missed abortion, consanguinity of parents, and family history of cancer were not significantly different in cases with and without a congenital malformation. The most frequent cancers were central nervous system tumors and lymphomas. No remarkable association between a particular anomaly and a specific cancer type could be shown. The high incidence of congenital anomalies in this study may stimulate future large cohort studies in our country.
我们利用患者记录评估了566名淋巴瘤和实体瘤患儿(中位年龄:8岁,男女性别比为1.3)先天性畸形的发生率。在本研究中,12.7%的儿童患有先天性畸形(7.8%)或胎记(4.9%)。儿童癌症综合征患者的发生率为3%,这些病例发展为典型肿瘤。近亲结婚率为12.6%,癌症家族史阳性率为31.2%。有或无先天性畸形的病例在癌症诊断时的中位年龄、性别、母亲年龄、死产和稽留流产史、父母近亲关系以及癌症家族史方面无显著差异。最常见的癌症是中枢神经系统肿瘤和淋巴瘤。未发现特定异常与特定癌症类型之间存在显著关联。本研究中先天性异常的高发生率可能会促使我国未来开展大型队列研究。