Kan A E, Rogers M
Institute of Pathology, Royal Alexandra Hospital for Children, Sydney, N.S.W., Australia.
Pediatr Dermatol. 1989 Jun;6(2):68-75. doi: 10.1111/j.1525-1470.1989.tb01001.x.
A female infant had the typical cutaneous and soft tissue lesions of juvenile hyaline fibromatosis with the characteristic histologic and ultrastructural features of the disease. Her clinical course and autopsy findings strongly resembled those of infantile systemic hyalinosis, suggesting that the two conditions may be parts of a spectrum.
一名女婴患有青少年透明纤维瘤病典型的皮肤和软组织病变，具有该疾病特征性的组织学和超微结构特征。她的临床病程和尸检结果与婴儿系统性透明变性极为相似，提示这两种病症可能属于同一谱系的不同部分。
