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蜡样脂褐质沉积症的皮肤超微结构诊断

Cutaneous ultrastructural diagnosis of ceroid-lipofuscinosis.

作者信息

Ishii M, Takahashi K, Hamada T, Tanaka A, Higami S

出版信息

Br J Dermatol. 1981 May;104(5):581-5. doi: 10.1111/j.1365-2133.1981.tb08176.x.

Abstract

A skin biopsy from a 6-year-old girl was examined by electron microscopy and the diagnosis of ceroid-lipofuscinosis (CL) was confirmed. This has not been reported in the dermatology literature, because of the absence of specific skin manifestations. However, as we have shown, various cells of skin, including fibroblasts, Schwann cells, eccrine serous cells, endothelial cells and smooth muscle cells, accumulated characteristic substances to produce the finger print pattern (FPP) or the curvilinear profile (CLP) which are thought to be diagnostic for CL. Cutaneous ultrastructural research in such cases is important as asymptomatic skin disorders may exist in other congenital storage diseases.

摘要

对一名6岁女孩的皮肤活检标本进行了电子显微镜检查,确诊为蜡样脂褐质沉积症(CL)。由于缺乏特异性皮肤表现,这在皮肤病学文献中尚未见报道。然而,正如我们所表明的,皮肤的各种细胞,包括成纤维细胞、施万细胞、汗腺浆液细胞、内皮细胞和平滑肌细胞,都会积累特征性物质,产生指纹样结构(FPP)或曲线样结构(CLP),这些被认为是CL的诊断依据。在这类病例中进行皮肤超微结构研究很重要,因为其他先天性贮积病可能存在无症状的皮肤疾病。

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