Beckett J H, Jacobs A H
Pediatrics. 1977 Mar;59(3):401-6.
Two new cases that conform to the clinical and histopathological features of recurring digital fibrous tumor of childhood, described by Reye in 1965, are reported. This tumor, which is considered a distinct entity among the juvenile fibromatoses, characteristically presents in infancy and early childhood, involves only the digits, recurs frequently following surgical excision without metastatic spread, and demonstrates the distinct histopathological finding of intracytoplasmic inclusion bodies within proliferated fibroblasts. This tumor is reviewed with reference to clinical features, histopathology, etiological considerations, and management.
报告了两例符合1965年Reye所描述的儿童复发性指纤维瘤临床和组织病理学特征的新病例。这种肿瘤在青少年纤维瘤病中被认为是一种独特的实体，典型地出现在婴儿期和儿童早期，仅累及手指，手术切除后经常复发但无转移扩散，并在增生的成纤维细胞内显示出胞质内包涵体这一独特的组织病理学表现。本文参考临床特征、组织病理学、病因学考量及治疗方法对该肿瘤进行了综述。
