Benichou M, Balmes P, Marty-Double C H, Allieu Y
Service de Chirurgie Orthopédique et Chirurgie de la Main, Hôpital Lapeyronie CHU, Montpellier.
Ann Pediatr (Paris). 1990 Mar;37(3):181-4.
Juvenile aponeurotic fibroma, isolated in 1953 by Louisa Keasbey is a rare tumour which is characterized by its recurrence and infiltration, but which has no tendency to metastasis. The case we report differs in its long-term outcome. The tumour diagnosed in a seven-year-old child has recurred locally for seven years, necessitated hand amputation, and finally developed a fibroblastic process extending to lung and pleura which caused the child's death. This new finding in Keasbey's disease led us to reconsider the nosological situation in juvenile fibromatoses and its reputation for benignity.
青少年腱膜纤维瘤由路易莎·基斯贝于1953年首次发现，是一种罕见的肿瘤，其特点是易复发和浸润，但无转移倾向。我们报告的这个病例在长期预后方面有所不同。该肿瘤在一名7岁儿童中被诊断出，已经局部复发了7年，最终不得不进行手部截肢，并且最终发展为成纤维细胞病变，扩散至肺部和胸膜，导致患儿死亡。基斯贝病的这一新发现促使我们重新审视青少年纤维瘤病的疾病分类情况及其良性的声誉。
