Stosiek N, Hornstein O P, Hiller D, Peters K P
Department of Dermatology, University of Erlangen-Nuremberg, Germany.
Dermatology. 1994;189(3):278-82. doi: 10.1159/000246861.
The association of connate, left-sided, extensive epidermal verrucous nevus, multiple isolated bone tumors and vitamin-D-resistant rickets since childhood seen in a 20-year-old male patient corresponded to an epidermal nevus syndrome (ENS). However, other organ involvement occasionally associated with ENS could not be found in this patient, and his intraosseous tumors represented histologically benign hemangiomas. Serum analysis revealed hypophosphatemia (together with phosphaturia), decreased levels of 1,25-dihydroxycholecalciferol and elevated levels of alkaline phosphatase indicating hypophosphatemic osteomalacia. Therefore we suppose that vitamin-D-resistant rickets combined with skeletal tumors represents a peculiar type of osteomalacia caused by unilateral mesenchymomas.
一名20岁男性患者自童年起就患有先天性左侧广泛性表皮疣状痣、多发性孤立性骨肿瘤和维生素D抵抗性佝偻病,这符合表皮痣综合征(ENS)。然而,该患者未发现ENS偶尔相关的其他器官受累情况,其骨内肿瘤组织学表现为良性血管瘤。血清分析显示低磷血症(伴有磷尿症)、1,25 - 二羟胆钙化醇水平降低和碱性磷酸酶水平升高,提示低磷性骨软化症。因此,我们推测维生素D抵抗性佝偻病合并骨骼肿瘤代表了一种由单侧间叶瘤引起的特殊类型的骨软化症。