皮肤血管肉瘤诊断和治疗的最新进展。

IF 2.1 4区 医学 Q3 DERMATOLOGY Cutis Pub Date : 2024-05-01 DOI:10.12788/cutis.1008
Elizabeth Richards, Joshua Schimmel, Michael Renzi, Naomi Lawrence
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引用次数: 0

摘要

皮肤血管肉瘤(CAS)是一种罕见的侵袭性恶性肿瘤,最常见于60岁以上的白种男性,通常表现为头部、颈部或头皮上的肿大瘀斑。边缘阴性的手术是一线治疗方法。莫氏显微摄影手术(MMS)的作用尚不确定,但可用于头颈部较小、周界清晰的病变。皮肤科医生在 CAS 的治疗中能发挥的最大作用是通过全面的全身皮肤检查和提高认识来缩短诊断时间。在高质量的证据允许制定共识指南之前,在专门治疗罕见难治肿瘤的癌症中心进行多学科治疗对于优化患者预后至关重要。
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An Update on Cutaneous Angiosarcoma Diagnosis and Treatment.

Cutaneous angiosarcoma (CAS) is a rare aggressive malignancy that most commonly manifests in White men older than 60 years and often appears as an enlarging ecchymosis on the head, neck, or scalp. Surgery with negative margins is the first-line treatment. The role of Mohs micrographic surgery (MMS) is uncertain but can be used in smaller, well-circumscribed lesions on the head and neck. The greatest impact that dermatologists can have in the management of CAS is through a thorough total-body skin examination and heightened awareness resulting in a shortened time to diagnosis. Until quality evidence allows for the creation of consensus guidelines, multidisciplinary care at a cancer center that specializes in rare difficult-to-treat tumors is essential in optimizing patient outcomes.

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来源期刊
Cutis
Cutis 医学-皮肤病学
CiteScore
1.10
自引率
0.00%
发文量
191
审稿时长
6-12 weeks
期刊介绍: Published since 1965, Cutis is a peer-reviewed clinical journal for the dermatologist, allergist, and general practitioner. The journal is published monthly and focuses on concise clinical articles that present the practical side of dermatology. Referenced in Index Medicus/MEDLINE, it is respected and enjoyed by both specialists and derm-active generalists, enabling its readers to get what they need quickly and efficiently. Furthermore, Cutis is read by more physicians actively involved in the day-to-day treatment of dermatologic conditions than any other dermatology publication. Covering a broad range of pertinent and timely topics, Cutis is written and edited by industry leaders. For information on article submissions, please see our Information for Authors.
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