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溶酶体贮积病皮肤活检标本的超微结构:诊断中常见的错误来源

Ultrastructure of skin biopsy specimens in lysosomal storage diseases: common sources of error in diagnosis.

作者信息

Sipe J C, O'Brien J S

出版信息

Clin Genet. 1979 Feb;15(2):118-25. doi: 10.1111/j.1399-0004.1979.tb01750.x.

Abstract

Common sources of error in the diagnosis of lysosomal storage diseases by ultrastructural examination of skin specimens have been identified in a series of biopsies from 72 patients. Four principal factors have emerged as leading pitfalls and sources of error in diagnosis. First, the skin biopsy technique itself may lead to alterations of normal skin ultrastructure. Second, artifacts may be produced during fixation and preparation of tissue for electron microscopy. Third, cellular organelles and structures normally present in human skin may be mistakenly interpreted as pathological. Fourth, the use of cultured skin fibroblasts for ultrastructural identification of storage material is often accompanied by artifacts induced in tissue culture and is not recommended. Recognition of these common problems may aid interpretation of the fine structure of skin abnormalities. Furthermore, when skin biopsy specimens are used as the primary source of diagnostic material, correlation of both skin ultrastructure and assay for specific lysosomal enzymes in cultured dermal fibroblasts will facilitate diagnostic accuracy.

摘要

通过对72例患者的一系列皮肤活检标本进行超微结构检查,已确定了溶酶体贮积病诊断中常见的误差来源。四个主要因素已成为诊断中的主要陷阱和误差来源。首先,皮肤活检技术本身可能导致正常皮肤超微结构的改变。其次,在组织固定和电子显微镜标本制备过程中可能会产生假象。第三,人类皮肤中正常存在的细胞器和结构可能会被错误地解释为病理性的。第四,使用培养的皮肤成纤维细胞进行贮积物质的超微结构鉴定时,常常伴随着组织培养中诱导产生的假象,因此不建议使用。认识到这些常见问题可能有助于解释皮肤异常的精细结构。此外,当皮肤活检标本用作诊断材料的主要来源时,将皮肤超微结构与培养的真皮成纤维细胞中特定溶酶体酶的检测结果相关联,将有助于提高诊断准确性。

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