Drouin C A, Mongrain E, Sasseville D, Bouchard H L, Drouin M
Service de Dermatologie, L'Hôtel-Dieu de Quèbec, Canada.
J Am Acad Dermatol. 1993 Feb;28(2 Pt 2):301-5. doi: 10.1016/0190-9622(93)70040-z.
Rothmund-Thomson syndrome is a rare genodermatosis that features a progressive, early-onset poikiloderma, a high incidence of juvenile cataracts, stunted growth, and a wide range of skeletal abnormalities. We report the seventh case of osteosarcoma in a patient with Rothmund-Thomson syndrome and review the previous reports describing this association.
罗思蒙德-汤姆森综合征是一种罕见的遗传性皮肤病，其特征为进行性早发性皮肤异色症、青少年白内障高发、生长发育迟缓以及多种骨骼异常。我们报告了第7例罗思蒙德-汤姆森综合征患者发生骨肉瘤的病例，并回顾了之前描述这种关联的报告。
