首页> 外文期刊>Journal of plastic, reconstructive & aesthetic surgery: JPRAS >Dermatofibrosarcoma protuberans in children and adolescents: Clinical presentation, histology, treatment, and review of the literature
【24h】

Dermatofibrosarcoma protuberans in children and adolescents: Clinical presentation, histology, treatment, and review of the literature

机译:儿童和青少年隆突性皮肤皮肤肉瘤:临床表现,组织学,治疗方法和文献复习

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose Dermatofibrosarcoma protuberans (DFSP) is a rare, low-grade malignant tumor. It is characterized by aggressive local infiltration, leading to a propensity for recurrence. In children, DFSP is even less common and likely misdiagnosed or underdiagnosed. This study is a review of DFSP in the pediatric population and aims to identify factors for successful treatment. Materials and methods From July of 1986 to 2011, a total of 159 patients were diagnosed with dermatofibrosarcoma protuberans at Kaohsiung Chang Gung Memorial Hospital, Taiwan. Subject to the age classification of our institution, patients under the age of 18 are defined in the pediatric category, of which159 cases were identified as our research subjects. Detailed data, including demographic data, imaging studies, pathology, treatment methods, and outcomes, of these identified patients were collected, reviewed, and analyzed. Results A total of 13 patients, consisting of six male and seven female patients, were identified based on our criteria. Two had the lesions noticed at birth. Most patients experienced a variable period of quiescence, followed by a rapid growth phase. All 13 patients underwent wide excisions. Post-excision reconstruction included direct closure in three cases, skin grafting in three cases, and local or free flap reconstruction in seven cases. Of 13 patients, four received postoperative radiotherapy. All patients survived without recurrence up to July 2011, with follow-up periods ranging from 20 months to 19 years. Conclusion Clinicians should be aware that DFSP is known to occur among children. Owing to its relatively low incidence, its presence may be confused with commoner lesions such as hemangioma, fibroma, or atrophic plaques without nodule. The confusing situation, as a result, frequently leads to delayed diagnosis. Vigilance in its diagnosis allows for treatment at manageable sizes as well as ensures complete excision. Reconstructive options, such as skin grafting, and modalities, such as adjuvant postoperative radiotherapy, are suggested to best complement each other. The former minimizes disfigurement while the latter minimizes recurrences.
机译:目的隆突性皮肤皮肤肉瘤(DFSP)是一种罕见的低度恶性肿瘤。其特征是侵袭性局部浸润,导致复发的倾向。在儿童中,DFSP甚至更不常见,并且可能被误诊或诊断不足。这项研究是对儿科人群中DFSP的综述,旨在确定成功治疗的因素。材料和方法1986年7月至2011年,台湾高雄市长庚纪念医院共诊断出159例隆突性皮肤皮肤肉瘤患者。根据我们机构的年龄分类,在儿科类别中定义了18岁以下的患者,其中159例被确定为我们的研究对象。收集,审查和分析了这些已鉴定患者的详细数据,包括人口统计学数据,影像学研究,病理学,治疗方法和结果。结果根据我们的标准,共鉴定出13例患者,其中6例男性和7例女性。有两个在出生时就注意到了病变。大多数患者处于不同的静止期,然后进入快速生长阶段。全部13例患者均行广泛切除。切除后重建包括三例直接闭合,三例皮肤移植和七例局部或游离皮瓣重建。 13例患者中,有4例接受了术后放疗。所有患者存活至2011年7月,无复发,随访期为20个月至19年。结论临床医生应注意,DFSP已知发生在儿童中。由于其发病率相对较低,其存在可能与常见的病变(如血管瘤,纤维瘤或无结节的萎缩性斑块)相混淆。结果,令人困惑的情况经常导致诊断延迟。诊断时保持警惕,可以以可控制的大小进行治疗,并确保完全切除。建议重建性选择(例如植皮)和模式(例如辅助术后放疗)可以最好地相互补充。前者最大程度地减少了毁容,而后者最大程度地减少了复发。

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