...
首页> 外文期刊>Melanoma research >Melanocytic schwannoma of the cutaneous and subcutaneous tissues: three cases and a review of the literature.
【24h】

Melanocytic schwannoma of the cutaneous and subcutaneous tissues: three cases and a review of the literature.

机译:皮肤和皮下组织黑素细胞性神经鞘瘤:三例并文献复习。

获取原文
获取原文并翻译 | 示例

摘要

Melanocytic schwannoma is a rare soft-tissue tumor, which arises most commonly in the paraspinal sympathetic chain. In general, 25% of the patients develop metastasis. To date, only 17 cases of a cutaneous and subcutaneous melanocytic schwannoma have been reported. None of these patients developed metastasis. Three cases of cutaneous melanocytic schwannoma, diagnosed in our institution are reported. For further literature overview we performed a search on Medline using the terms 'melanocytic schwannoma' or 'melanotic schwannoma' or 'Carney complex' combined with 'skin' or 'cutaneous', for the period 1970-2007. Seventeen patients were described to have melanocytic schwannoma of the skin or subcutaneous tissues. These papers were reviewed for clinical data. Two of the three patients showed metastatic disease, one of them died of disseminated metastases. In contrast, none of the reported cases of cutaneous or subcutaneous melanocytic schwannomas was characterized by a malignant course. The differential diagnosis, especially with regard to malignant melanoma, is made by histology and by its clinical course, which differs from melanoma in its tendency to recur at the site of excision and slow rate of growth. Commonly misdiagnosed as melanoma, this tumor reveals insights into the origin of both melanocytes and Schwann cells. It is likely that the biological bases for melanoma and melanocytic schwannoma differ. It is necessary to differentiate this tumor from melanoma because of the differing prognosis and the association of melanocytic schwannoma with the Carney complex. Owing to the lack of clinical trials, we recommend that patients be treated according to the existing guidelines for melanoma.
机译:黑素细胞性神经鞘瘤是一种罕见的软组织肿瘤,最常见于椎旁交感神经链。通常,有25%的患者发生转移。迄今为止,仅报道了17例皮肤和皮下黑素细胞性神经鞘瘤。这些患者均未发生转移。报告了在我院诊断出的三例皮肤黑素细胞性神经鞘瘤。为进一步了解文献,我们在1970-2007年期间对Medline进行了搜索,使用术语“黑素细胞性神经鞘瘤”或“黑色素细胞性神经鞘瘤”或“卡尼复合体”与“皮肤”或“皮肤”组合。据描述有十七名患者的皮肤或皮下组织有黑素细胞性神经鞘瘤。这些论文进行了临床数据审查。三名患者中有两名表现出转移性疾病,其中一名死于弥漫性转移。相反,没有报告的皮肤或皮下黑素细胞神经鞘瘤病例以恶性病程为特征。鉴别诊断,特别是关于恶性黑色素瘤,是通过组织学和临床过程进行的,与黑色素瘤的区别在于其在切除部位复发的趋势和缓慢的生长速度。通常被误诊为黑色素瘤,这种肿瘤揭示了对黑色素细胞和雪旺细胞起源的见解。黑色素瘤和黑素细胞性神经鞘瘤的生物学基础可能不同。由于黑色素细胞性神经鞘瘤与卡尼复合体的预后不同,因此有必要将该肿瘤与黑色素瘤区分开。由于缺乏临床试验,我们建议根据现有的黑色素瘤指南对患者进行治疗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号