Indian Journal of Dermatology | |
Juvenile hyaline fibromatosis | |
关键词: Autosomal recessive disease; fibrillary matrix; glycosaminoglycans; Juvenile hyaline fibromatosis; Periodic acid Schiff; | |
DOI : 10.4103/0019-5154.91840 | |
来源: DOAJ |
【 摘 要 】
Juvenile hyaline fibromatosis is a rare, autosomal-recessive disease characterized by papular and nodular skin lesions, gingival hyperplasia, joint contractures and bone involvement in variable degrees. It is a connective tissue disorder with aberrant synthesis of glycosaminoglycans by fibroblasts. We report a 5-year-old female born of first-degree consanguineous marriage who presented with multiple, recurrent, painless, variable-sized nodules. Fine needle aspiration cytology smears and the subsequent histopathological examination from the nodules showed benign spindle cells in a Periodic acid Schiff-positive myxoid background. The disease has a relentlessly progressive course, with most patients surviving only up to the 4 th decade. As of now, there is no specific treatment for this disorder. Genetic counseling is essential to explain to parents about a 25% chance of having a diseased baby in any pregnancy. With the gene being mapped recently, techniques for antenatal diagnosis are likely to be established.
【 授权许可】
Unknown