Suppr超能文献

“非典型斯皮茨瘤”患者的前哨淋巴结活检。12例报告。

Sentinel lymph node biopsy in patients with "atypical Spitz tumors." A report on 12 cases.

作者信息

Urso Carmelo, Borgognoni Lorenzo, Saieva Calogero, Ferrara Gerardo, Tinacci Galliano, Begliomini Brunero, Reali Umberto M

机构信息

Department of Anatomic Pathology, Dermatopathology Section, S. M. Annunziata Hospital, Florence, Italy.

出版信息

Hum Pathol. 2006 Jul;37(7):816-23. doi: 10.1016/j.humpath.2006.02.001. Epub 2006 May 19.

Abstract

The distinction between Spitz nevus and melanoma is currently possible, applying a set of definite histological criteria. However, in certain lesions deviating from the stereotypical morphology of classic Spitz nevi ("atypical Spitz tumors"), the differentiation between benign and malignant cases appears problematic because objective criteria for a reliable diagnosis are lacking. We report the clinicopathologic findings of 12 patients with atypical Spitz tumors, who underwent sentinel node biopsy. All the tumors, composed of spindle and/or epithelioid cells, histologically showed features referable to Spitz nevi mixed to features generally found in malignant melanomas. Nine patients were females and three males, ranging in age from 2 to 48 years (mean, 23.2 years). The size of lesions ranged from 5 to 9 mm, the thickness from 1.12 to 5.70 mm. Nodal micrometastases were found in 4 (33.3%) patients. Among the patients with positive sentinel node, two showed minimal nodal involvements; one patient showed additional tumor deposits in one nonsentinel regional node. All patients are alive and free of disease with a follow-up of 2 to 90 months (mean, 26.3 months). Metastasizing and nonmetastasizing cases appeared clinically and histologically indistinguishable. The statistical analysis showed no significant difference between the two groups. Results suggested that all the reported cases may constitute a relatively homogeneous morphological group of lesions with a relevant metastatic potential that may be underdiagnosed.

摘要

目前,应用一套明确的组织学标准可以区分Spitz痣和黑色素瘤。然而,在某些偏离经典Spitz痣典型形态的病变(“非典型Spitz肿瘤”)中,良性和恶性病例的鉴别似乎存在问题,因为缺乏可靠诊断的客观标准。我们报告了12例接受前哨淋巴结活检的非典型Spitz肿瘤患者的临床病理结果。所有肿瘤均由梭形和/或上皮样细胞组成,组织学上显示出符合Spitz痣的特征,并混合有通常在恶性黑色素瘤中发现的特征。9例为女性,3例为男性,年龄从2岁至48岁不等(平均23.2岁)。病变大小从5毫米至9毫米不等,厚度从1.12毫米至5.70毫米不等。4例(33.3%)患者发现有淋巴结微转移。在前哨淋巴结阳性的患者中,2例显示淋巴结受累轻微;1例患者在一个非前哨区域淋巴结中有额外的肿瘤沉积物。所有患者均存活且无疾病,随访时间为2至90个月(平均26.3个月)。发生转移和未发生转移的病例在临床和组织学上无法区分。统计分析显示两组之间无显著差异。结果表明,所有报告的病例可能构成一组形态相对一致的病变,具有相关的转移潜能,可能存在诊断不足的情况。

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