Smith N M, Thornton C M
Department of Paediatric Pathology and Cytogenetics, Royal Hospital for Sick Children, Edinburgh, Scotland.
Pediatr Pathol Lab Med. 1996 Jul-Aug;16(4):673-80.
A congenital fetal rhabdomyoma was removed from the neck of a male infant on the second day of life. The lesion recurred 10 years later with histological features suggestive of increased differentiation and no evidence of malignant transformation. An unrelated patient of 3 years suffered from a recurrent fetal rhabdomyoma 4 months after the initial resection. The possibility of early or late recurrence must be considered when a diagnosis of fetal-type rhabdomyoma is made.
一名男婴出生第二天,颈部的先天性胎儿横纹肌瘤被切除。10年后该病变复发,组织学特征提示分化增加,无恶性转化证据。一名3岁的非相关患者在初次切除后4个月,胎儿横纹肌瘤复发。诊断胎儿型横纹肌瘤时,必须考虑早期或晚期复发的可能性。