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隆突性皮肤纤维肉瘤的临床病理特征

Clinicopathological features of dermatofibrosarcoma protuberans.

作者信息

Larbcharoensub Noppadol, Kayankarnnavee Jitchai, Sanpaphant Suda, Kiranantawat Kidakorn, Wirojtananugoon Chewarat, Sirikulchayanonta Vorachai

机构信息

Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.

Department of Surgery, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.

出版信息

Oncol Lett. 2016 Jan;11(1):661-667. doi: 10.3892/ol.2015.3966. Epub 2015 Nov 24.

DOI:10.3892/ol.2015.3966
PMID:26870263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4726970/
Abstract

Dermatofibrosarcoma protuberans (DFSP) is a superficial cutaneous tumor of low malignant potential characterized by a high rate of local recurrence. The histopathological appearance shows uniform spindle neoplastic cells arranged in a predominantly storiform pattern, typically with positive staining for cluster of differentiation (CD)34 and vimentin on immunohistochemistry. A minority of cases of DFSP have areas of sarcomatous transformation. Wide surgical excision is the cornerstone of treatment for DFSP. The objective of the present study was to determine the clinicopathological features of DFSP. Pathological records were searched for cases of DFSP in the database of the Department of Pathology, Faculty of Medicine Ramathibodi Hospital (Mahidol University, Bangkok, Thailand) between 1994 and 2013. The results showed 68 cases with DFSP. The mean age at diagnosis was 40 years (range, 3-86 years). Among this group of patients, 26 cases (38.2%) experienced local recurrence and 6 (8.8%) exhibited sarcomatous transformation of DFSP. The factors that predict the recurrence of DFSP are an incorrect first pathological diagnosis and an inadequate surgical margin. The factors that predict the sarcomatous transformation of DFSP are a larger tumor size and an incorrect first pathological diagnosis. In patients who have tumors with spindle cells arranged in a storiform pattern, CD34 immunohistochemical staining provides the definitive diagnosis. Exact histopathological categorization is important to select the appropriate treatment and predict the clinical outcome.

摘要

隆突性皮肤纤维肉瘤(DFSP)是一种潜在恶性程度较低的浅表皮肤肿瘤,其特点是局部复发率高。组织病理学表现为一致的梭形肿瘤细胞,主要呈车辐状排列,免疫组织化学检查通常显示分化簇(CD)34和波形蛋白染色阳性。少数DFSP病例有肉瘤样转化区域。广泛手术切除是DFSP治疗的基石。本研究的目的是确定DFSP的临床病理特征。在拉玛提波迪医院医学院病理科(泰国曼谷玛希隆大学)数据库中检索1994年至2013年期间的DFSP病例的病理记录。结果显示有68例DFSP病例。诊断时的平均年龄为40岁(范围3 - 86岁)。在这组患者中,26例(38.2%)出现局部复发,6例(8.8%)表现为DFSP的肉瘤样转化。预测DFSP复发的因素是首次病理诊断错误和手术切缘不足。预测DFSP肉瘤样转化的因素是肿瘤体积较大和首次病理诊断错误。对于具有呈车辐状排列的梭形细胞肿瘤的患者,CD34免疫组织化学染色可提供明确诊断。准确的组织病理学分类对于选择合适的治疗方法和预测临床结果很重要。

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Low recurrence rate after surgery for dermatofibrosarcoma protuberans: a multidisciplinary approach from a single institution.隆突性皮肤纤维肉瘤手术后的低复发率:来自单一机构的多学科方法。
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