首页> 外文期刊>Diagnostic cytopathology >Fine-needle aspiration cytology features of a recurring plexiform fibrohistiocytic tumor in the upper limb and review of the literature.
【24h】

Fine-needle aspiration cytology features of a recurring plexiform fibrohistiocytic tumor in the upper limb and review of the literature.

机译:上肢复发性丛状纤维组织细胞性肿瘤的细针穿刺细胞学特征及文献复习。

获取原文
获取原文并翻译 | 示例
           

摘要

Plexiform fibrohistiocytic tumor is a rare soft tissue tumor that has a propensity to occur in the extremities in adolescents and young adults. Its cytologic features are not well documented, with only two case reports available in the literature. We present the case of a recurrent plexiform fibrohistiocytic tumor in a 19-year-old male, the cytologic features of which mimic that of a high-grade sarcoma. We discuss the likely differential diagnosis based on the cytologic findings and a review of the current literature on this highly unusual tumor is also performed.
机译:丛状纤维组织细胞肿瘤是一种罕见的软组织肿瘤,在青少年和年轻人的四肢都有发生的倾向。其细胞学特征尚未得到充分记录,文献中仅有两个病例报告。我们介绍了一名19岁男性复发性丛状纤维组织细胞瘤的病例,其细胞学特征与高度肉瘤相似。我们讨论了基于细胞学发现的可能的鉴别诊断,并且还对这种高度罕见的肿瘤进行了文献综述。

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