Matsuo M, Nakamura S, Matsuo M, Hamasaki Y, Miyazaki S, Watanabe T
Acta Paediatr Jpn. 1989 Oct;31(5):605-8. doi: 10.1111/j.1442-200x.1989.tb01362.x.
We report an unusual case of fibromatous disease in infancy, diagnosed as a multiple infantile fibromatosis of unclassified type. Histologically, the tumors are composed of a mixture of fibrous component and mature adipose tissue. The clinical manifestations resemble those of infantile myofibromatosis. The symptoms, including size and number of tumors, have not been progressive for one year.
我们报告了一例婴儿期纤维瘤病的罕见病例，诊断为未分类型多发性婴儿纤维瘤病。组织学上，肿瘤由纤维成分和成熟脂肪组织混合组成。临床表现类似于婴儿肌纤维瘤病。包括肿瘤大小和数量在内的症状一年来未进展。
