Lubec B, Steinert I, Breier F, Jurecka W, Pillwein K, Fang-Kircher S
Department of Paediatrics (Neonatology), University of Vienna, Austria.
Arch Dis Child. 1995 Sep;73(3):246-8. doi: 10.1136/adc.73.3.246.
Juvenile hyaline fibromatosis is a rare disorder characterised by multiple subcutaneous tumours, gum hypertrophy, muscle weakness, and flexion contractures of the large joints. Histology shows an abundance of a homogenous, amorphous, acidophilic extracellular matrix in which spindle shaped cells are embedded forming minute streaks. It has been previously suggested that collagen abnormalities may be involved. A 14 month old girl with this syndrome is described in whom postmortem western blot studies were performed. These studies revealed an absent pro-alpha 2(I) chain and an absent collagen type III chain in skin but not in the other organs examined.
青少年透明纤维瘤病是一种罕见的疾病,其特征为多发性皮下肿瘤、牙龈肥大、肌肉无力以及大关节的屈曲挛缩。组织学显示有大量均匀、无定形、嗜酸性的细胞外基质,其中嵌入梭形细胞形成微小条纹。此前有人提出可能涉及胶原蛋白异常。本文描述了一名患有该综合征的14个月大女孩,对其进行了死后蛋白质印迹研究。这些研究显示,皮肤中缺乏前α2(I)链和III型胶原链,但在所检查的其他器官中未发现。