Schmoeckel C, Hohlfed M
Arch Dermatol Res. 1979 Oct;266(2):187-96. doi: 10.1007/BF00694628.
An ultrastructural investigation of two cutaneous lesions in a two-year-old Turkish boy with disseminated lipogranulomatosis (Farber) revealed curvilinear bodies in fibroblasts, histiocytes, and endothelial cells; "elongated membranes" in fibroblasts and endothelial cells; "zebra bodies" in endothelial cells; and spindle-shaped bodies in Schwann cells. In peripheral lymphocytes only alterations of mitochondria (swelling and ruptured cristae) but no inclusion bodies were found. Curvilinear bodies were numerous and easily identifiable; they appear to be characteristic of Farber's disease, and naming them "Farber bodies" is proposed. The diagnosis of this ceramide storage disease, in which the histological examination is relatively unspecific, can therefore be confirmed ultrastructurally.
对一名患有播散性脂肪肉芽肿病(法伯病)的两岁土耳其男孩的两处皮肤病变进行的超微结构研究显示,在成纤维细胞、组织细胞和内皮细胞中存在曲线体;在成纤维细胞和内皮细胞中存在“拉长的膜”;在内皮细胞中存在“斑马体”;在施万细胞中存在纺锤体。在外周淋巴细胞中仅发现线粒体改变(肿胀和嵴破裂),但未发现包涵体。曲线体数量众多且易于识别;它们似乎是法伯病的特征,建议将其命名为“法伯体”。因此,这种神经酰胺贮积病的诊断在组织学检查相对不具特异性的情况下,可以通过超微结构得到证实。