Caylakli Fatma, Cakmak Ozcan, Seckin Deniz, Kayaselcuk Fazilet, Demirhan Beyhan, Ozluoglu Levent Naci
Faculty of Medicine, Department of Otorhinolaryngology, Baskent University, Ankara, Turkey.
Int J Pediatr Otorhinolaryngol. 2003 May;67(5):557-61. doi: 10.1016/s0165-5876(03)00017-x.
Juvenile hyaline fibromatosis (JHF) is a rare disease with autosomal recessive inheritance. It is characterized by papulonodular skin lesions which are painless but cosmetically unacceptable, and often disturb normal joint function. The nose, chin, ears, scalp, back, and knees are the most common affected sites. In some cases, gingival hypertrophy, flexion contractures of the large joints, osteolytic bone lesions, and stunted growth may be associated with skin lesions. We report a 9-year-old girl presented with a soft, painless, slow growing, tumoral mass on the supratip of her nose. The lesion was totally excised with open rhinoplasty approach and histopathological diagnosis was JHF.
青少年透明纤维瘤病(JHF)是一种常染色体隐性遗传的罕见疾病。其特征为丘疹结节性皮肤病变,无痛但影响美观,且常干扰正常关节功能。鼻子、下巴、耳朵、头皮、背部和膝盖是最常受累的部位。在某些情况下,牙龈增生、大关节屈曲挛缩、溶骨性骨病变和生长发育迟缓可能与皮肤病变相关。我们报告一名9岁女孩,其鼻尖上方出现一个柔软、无痛、生长缓慢的肿瘤性肿块。采用开放式鼻整形术方法将病变完全切除,组织病理学诊断为青少年透明纤维瘤病。