Mansur A Tülin, Yasar Sirin, Aydingöz Ikbal Esen, Göktay Fatih, Ozdemir Nilgün, Sungurlu Faik
Dermatology Clinic, Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey.
J Cutan Pathol. 2007 Apr;34(4):342-5. doi: 10.1111/j.1600-0560.2006.00610.x.
Lipedematous scalp (LS) is a rare condition of unknown etiology characterized by a thick, boggy scalp that occurs mostly in adult black females. The main pathologic finding consists of increased thickness of scalp resulting from thickening of the subcutaneous fat layer. Nevus lipomatosus superficialis (NLS) is an uncommon hamartomatous skin tumor characterized by soft, yellowish papules, or cerebriform plaques, usually localized on the buttock or thigh. Here, we report a 46-year-old woman who has NLS localized on the occipital area, accompanied by LS just beneath and peripheral area of this plaque. The diagnoses of NLS and LS were established by histopathological examination. In addition, the increase in subcutaneous fat layer was demonstrated using magnetic resonance imaging. The presented patient is the first case showing colocalization of NLS and LS.
脂肿性头皮(LS)是一种病因不明的罕见病症,其特征为头皮增厚、质地松软,多见于成年黑人女性。主要病理表现为皮下脂肪层增厚导致头皮厚度增加。浅表脂肪瘤样痣(NLS)是一种不常见的错构瘤性皮肤肿瘤,其特征为柔软的淡黄色丘疹或脑回状斑块,通常位于臀部或大腿。在此,我们报告一名46岁女性,其NLS位于枕部区域,该斑块下方及周边区域伴有LS。通过组织病理学检查确诊为NLS和LS。此外,利用磁共振成像显示了皮下脂肪层增厚。该病例是首例显示NLS和LS共定位的病例。