Beckwith-Wiedemann综合征2例并文献复习
Two Cases of Beckwith-Wiedemann Syndrome and Literature Review
DOI: 10.12677/acm.2025.153648, PDF,   
作者: 赵 伟, 赵艳霞, 王玲珍, 孙 妍, 杨 静*：青岛大学附属医院儿童血液肿瘤科，山东 青岛；林洪萍：莱州市妇幼保健院儿科，山东 烟台
关键词: Beckwith-Wiedemann综合征；肝母细胞瘤；肾母细胞瘤；Beckwith-Wiedemann Syndrome； Hepatoblastoma； Nephroblastoma
摘要: Beckwith-Wiedemann综合征是一种罕见的先天性过度生长疾病，患者通常表现为巨舌症、腹壁缺损、偏侧肢体肥大、腹部器官肿大，以及儿童早期患胚胎性肿瘤的风险增加。现报告本院收治的2例合并胚胎性肿瘤的BWS患儿的临床资料并复习相关文献，以期提高临床工作者对该病的认识。
Abstract: Beckwith-Wiedemann syndrome is a rare congenital overgrowth disorder, characterized by mega tongue, abdominal wall defects, unilateral limb hypertrophy, abdominal organ enlargement, and an increased risk of embryonic tumors in early childhood. This article reports the clinical data of two cases of BWS patients with concomitant embryonal tumors admitted to our hospital and reviews relevant literature in order to improve the understanding of this disease among clinical workers.
文章引用：赵伟, 林洪萍, 赵艳霞, 王玲珍, 孙妍, 杨静. Beckwith-Wiedemann综合征2例并文献复习[J]. 临床医学进展, 2025, 15(3): 556-561. https://doi.org/10.12677/acm.2025.153648

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