Suppr超能文献

用于黑色素瘤诊断的比较基因组杂交技术。

Comparative genomic hybridization for the diagnosis of melanoma.

作者信息

Vanison Christopher, Tanna Neil, Murthy Ananth S

出版信息

Eur J Plast Surg. 2010 Feb;33(1):45-48. doi: 10.1007/s00238-009-0369-9. Epub 2009 Dec 9.

Abstract

Despite advancements in protocols, a subset of melanocytic lesions continues to pose diagnostic challenges. This is particularly true in the pediatric population where certain congenital nevi mimic melanoma. Recently, comparative genomic hybridization (CGH) has been utilized to support diagnoses of melanocytic lesions based on DNA copy number changes. Because distinct differences in copy number changes have been shown to occur in malignant melanoma and benign nevi, CGH can be a useful adjunct when diagnosis based on histology alone is indeterminate. The authors discuss the benefits of using CGH to aid in the diagnosis of melanocytic lesions that are difficult to characterize as malignant or benign based on clinical and histologic features alone. This paper presents a brief clinical report and review of the literature. A 13-year-old Caucasian male presented to an academic tertiary care medical center after a shave biopsy unexpectedly revealed malignant melanoma with positive deep margins. Following complete excisional biopsy, the diagnosis of malignant melanoma with depth of 0.92 mm was confirmed, both by the home institution's pathologist and by consultant dermatopathologists at two separate academic tertiary medical centers. Sentinel lymph node biopsy revealed a small focus of metastatic melanoma, this lead to a left-sided modified radical neck dissection. All nodes removed were negative for disease, and surgical and postsurgical care was uncomplicated. Before proceeding with interferon therapy, CGH was performed on the tissue from the primary lesion. Other than a slight amplification of chromosome 16p, no other aberrations were detected favoring a benign lesion. Ultimately, the diagnosis was amended to compound melanocytic nevus of the nose with benign nevus cell rest in the sentinel node. While histopathologic evaluation is the current gold standard for the diagnosis of melanoma, there are many cases where it is inaccurate. The use of CGH in the evaluation of histologically equivocal lesions may allow certain patients to avoid invasive procedures and associated morbidities. The authors propose that, in these select diagnostically challenging cases, tissue analyses by CGH may be beneficial before proceeding to more invasive procedures such as sentinel node biopsy and complete lymphadenectomy.

摘要

尽管诊断方案有所进步,但仍有一部分黑素细胞性病变在诊断上存在挑战。这在儿科人群中尤为明显,某些先天性痣会与黑色素瘤相似。最近,比较基因组杂交(CGH)已被用于根据DNA拷贝数变化辅助黑素细胞性病变的诊断。由于已表明恶性黑色素瘤和良性痣在拷贝数变化上存在明显差异,当仅基于组织学的诊断不明确时,CGH可作为一种有用的辅助手段。作者讨论了使用CGH辅助诊断黑素细胞性病变的益处,这些病变仅根据临床和组织学特征难以判定为恶性或良性。本文呈现了一份简短的临床报告并对文献进行了综述。一名13岁的白人男性在刮除活检意外发现深部切缘阳性的恶性黑色素瘤后,就诊于一家学术性三级医疗中心。在进行完整切除活检后,该机构的病理学家以及另外两家学术性三级医疗中心的皮肤科病理会诊专家均确诊为深度为0.92毫米的恶性黑色素瘤。前哨淋巴结活检发现了一小处转移性黑色素瘤病灶,这导致患者接受了左侧改良根治性颈清扫术。所有切除的淋巴结均未发现病变,手术及术后护理过程顺利。在进行干扰素治疗之前,对原发性病变组织进行了CGH检测。除了16号染色体短臂有轻微扩增外,未检测到其他有利于良性病变的畸变。最终,诊断修正为鼻部复合性黑素细胞痣,前哨淋巴结中有良性痣细胞残留。虽然组织病理学评估是目前诊断黑色素瘤的金标准,但在许多情况下并不准确。在评估组织学上模棱两可的病变时使用CGH,可能会使某些患者避免侵入性手术及相关并发症。作者提出,在这些具有挑战性的特定诊断病例中,在进行如前哨淋巴结活检和完整淋巴结切除术等更具侵入性的手术之前,通过CGH进行组织分析可能有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0067/2837230/bb3e51549da5/238_2009_369_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验