Koylu Mehmet Talay, Uysal Yusuf, Kucukevcilioglu Murat, Ceylan Osman Melih, Deveci Mehmet Salih
Tatvan Military Hospital Ophthalmology Clinic , Bitlis , Turkey .
Orbit. 2014 Aug;33(4):295-7. doi: 10.3109/01676830.2014.902477. Epub 2014 May 15.
A subepidermal calcified nodule is an uncommon variant of calcinosis cutis and only a limited number of cases have been reported about the eyelid nodules in the literature. A 20-year-old male was referred to our department with symmetrical nodules on both upper eyelids enlarging over 3 years. Both nodules were removed by excisional biopsy. After the histopathologic evaluation, the diagnosis was subepidermal calcified nodule. He had a complete recovery with no recurrence and acceptable aesthetic appearance. As a rare entity, subepidermal calcified nodule should be thought in differential diagnosis of eyelid nodular lesions and symmetrical appearance may be seen.
表皮下钙化结节是皮肤钙质沉着症的一种罕见变体,文献中仅报道了少数眼睑结节病例。一名20岁男性因双侧上眼睑对称性结节3年多来不断增大而转诊至我科。两个结节均通过切除活检切除。经过组织病理学评估,诊断为表皮下钙化结节。他完全康复,无复发,外观良好。作为一种罕见疾病,在眼睑结节性病变的鉴别诊断中应考虑表皮下钙化结节,且可能出现对称性外观。