皮肤癌:回归基础

IF 0.2 Q4 DERMATOLOGY
J. Baumann, Andrew Groneck, Kari Martin
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引用次数: 0

摘要

隆突性皮肤纤维肉瘤是一种起源于真皮的软组织肿瘤。这种相对罕见的低级别肿瘤有很高的局部复发倾向,除非完全切除。隆突性皮肤纤维肉瘤通常进展缓慢,在年轻人的躯干上形成斑块。它通常像一个疤痕,在几个月到几年的时间里慢慢生长。由于它的罕见和微妙的进展,这种形式的皮肤癌通常会多年未被诊断出来。随着时间的推移,隆突性皮肤纤维肉瘤可侵入皮下脂肪、肌肉、筋膜和胸壁。诊断皮肤纤维肉瘤隆突是由核心针或切口活检。一旦确诊,治愈率接近100%。本文就皮肤纤维肉瘤的流行病学、病理生理学、临床特征、鉴别诊断、诊断、分期和治疗作一综述。提高医疗保健提供者对这种罕见形式的皮肤癌及其识别的认识可能会改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Skin Cancer: Back to Basics
Dermatofibrosarcoma protuberans is a soft tissue tumor that arises from the dermis. This relatively rare, low-grade tumor has a high propensity for local recurrence unless it is completely excised. Dermatofibrosarcoma protuberans classically progresses slowly as a plaque on the trunk of young adults. It often resembles a scar that is slowly growing over months to years. Because of its rarity and subtle progression, this form of skin cancer will often go undiagnosed for years. Over time, dermatofibrosarcoma protuberans can become invasive into the subcutaneous fat, muscle, fascia, and chest wall. Diagnosis of dermatofibrosarcoma protuberans is made by a core needle or incisional biopsy. Once diagnosed, cure rates approach 100%. The purpose of this article is to review the epidemiology, pathophysiology, clinical features, differential diagnosis, diagnosis, staging, and treatment of dermatofibrosarcoma protuberans. Increasing healthcare providers' awareness about this rare form of skin cancer and its recognition may improve patient outcomes.
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来源期刊
CiteScore
0.30
自引率
25.00%
发文量
45
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