Ali Nebras, Fast Sanne, Poulsen Mette Ramsdal, Bygum Anette
Hudafdeling I og Allergicentret, Odense Universitetshospital, Sdr. Boulevard 29, 5000 Odense C.
Ugeskr Laeger. 2015 Jan 26;177(2A):68-9.
Buschke-Ollendorff syndrome is a rare condition characterized by skin manifestations and osteopoikilosis. We describe a mother and her son who presented with indurated skin lesions suggestive of connective tissue naevi. X-rays showed multiple symmetrical foci of osteosclerosis. They had both been diagnosed earlier with Calvé-Legg-Perthes disease, which on revision most likely represented Buschke-Ollendorff syndrome. Buschke-Ollendorff syndrome may imitate Calvé-Legg-Perthes disease. Skin signs may be the clue to diagnosis. Main differentials are sclerotic bone metastases and osteoma.
布施克-奥伦多夫综合征是一种罕见疾病,其特征为皮肤表现和骨斑点症。我们描述了一位母亲及其儿子,他们出现了提示结缔组织痣的硬结性皮肤病变。X线显示多个对称性骨硬化灶。他们两人此前均被诊断为卡勒韦-莱格-佩尔茨病,经复查很可能为布施克-奥伦多夫综合征。布施克-奥伦多夫综合征可能会模仿卡勒韦-莱格-佩尔茨病。皮肤体征可能是诊断的线索。主要鉴别诊断包括硬化性骨转移瘤和骨瘤。