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组织学和遗传学证据表明,一种主要由大巢组成的浅表扩散性黑色素瘤变体。

Histological and genetic evidence for a variant of superficial spreading melanoma composed predominantly of large nests.

机构信息

Dermatopathologie Friedrichshafen, Friedrichshafen, Germany.

出版信息

Mod Pathol. 2012 Jun;25(6):838-45. doi: 10.1038/modpathol.2012.35. Epub 2012 Mar 2.

Abstract

Cutaneous melanomas are characterized by a range of histological appearances, and several morphological variants have been described. In this study, we report a variant of superficial spreading melanoma that is characterized by large, irregular junctional melanocytic nests. The junctional nests varied in shape and size, showed focal tendency to confluence, and were often surrounded by a cuff of epidermal keratinocytes. The melanocytes comprising the nests showed variable cytological atypia. In most of the cases, scant intraepidermal or junctional single melanocytes were seen, and other well-documented diagnostic criteria for melanoma were lacking, and as a result, histological recognition of these tumors as melanoma was difficult. Some cases were associated with an invasive dermal component or showed evidence of sun damage. To provide supporting evidence for malignancy, we analyzed these tumors for genomic aberrations. Using array comparative genomic hybridization (aCGH), we identified multiple genomic aberrations in all analyzed cases. A similar pattern of genomic aberrations was seen in a control group of bona fide superficial spreading melanomas, suggesting that these 'melanomas composed exclusively or predominantly of large nests' are indeed variants of superficial spreading melanoma. Fluorescence in-situ hybridization (FISH) was positive in 40% of the cases. However, using aCGH, the FISH-negative cases showed multiple genomic aberrations in regions that are not covered by FISH. The low sensitivity of the FISH test can be explained by the fact that FISH only evaluates four genomic loci for aberrations, whereas aCGH surveys the entire genome. In summary, we present histological and molecular genetic evidence for a morphological variant of superficial spreading melanoma. Awareness of the histological features will aid in their correct diagnosis as melanoma, and in difficult cases, judicious application of ancillary tests such as aCGH (rather than FISH) will assist accurate diagnosis.

摘要

皮肤黑色素瘤的组织学表现多样,已有多种形态学变异型被描述。本研究报告了一种特殊的浅表扩散性黑色素瘤,其特征为大而不规则的交界性巢状黑色素细胞。交界性巢状结构形态和大小不一,有局灶融合倾向,常被一层表皮角质形成细胞围绕。巢状结构中的黑色素细胞具有不同程度的细胞学异型性。大多数病例中,仅见稀疏的表皮内或交界性单个黑色素细胞,缺乏其他有明确诊断意义的黑色素瘤标准,因此,这些肿瘤的组织学诊断为黑色素瘤存在困难。部分病例伴有侵袭性真皮成分或有日光损伤的证据。为了提供恶性肿瘤的支持证据,我们对这些肿瘤进行了基因组异常分析。采用 array comparative genomic hybridization (aCGH),我们在所有分析的病例中均发现了多个基因组异常。一组真正的浅表扩散性黑色素瘤的对照病例中也出现了类似的基因组异常模式,表明这些“主要或完全由大巢状结构组成的黑色素瘤”确实是浅表扩散性黑色素瘤的变异型。荧光原位杂交 (FISH) 在 40%的病例中呈阳性。然而,使用 aCGH,FISH 阴性病例在 FISH 未覆盖的区域显示出多个基因组异常。FISH 检测的低敏感性可以用以下事实解释:FISH 仅评估四个基因组位点的异常,而 aCGH 则检测整个基因组。总之,我们提供了浅表扩散性黑色素瘤的形态学变异型的组织学和分子遗传学证据。了解这些组织学特征有助于正确诊断为黑色素瘤,在困难的病例中,明智地应用辅助检测方法,如 aCGH(而非 FISH),将有助于准确诊断。

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