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用咪喹莫特、他扎罗汀和5-氟尿嘧啶局部联合治疗非典型纤维黄色瘤。

Atypical Fibroxanthoma Treated with a Topical Combination of Imiquimod, Tazarotene, and 5-Fluorouracil.

作者信息

Nahm William J, Badiavas Evangelos V, Kirsner Robert S, Boyd Carter J, Arthur Anita A, Bae Sean, Shen John

机构信息

New York University Grossman School of Medicine, New York, NY, USA.

Dr. Phillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Dermatol Ther (Heidelb). 2024 Apr;14(4):1049-1056. doi: 10.1007/s13555-024-01127-x. Epub 2024 Mar 12.

Abstract

This case report describes an 80-year-old man who presented with a growing erythematous nodule with erosion, measuring 0.6 cm × 0.6 cm, on his right temple. This lesion was later diagnosed as atypical fibroxanthoma (AFX). Instead of undergoing Mohs surgery, the gold standard treatment, the patient opted to pursue a topical treatment regimen because of financial costs associated with surgical removal and repair. This topical regimen consisted of tazarotene cream, imiquimod cream, and 5-fluorouracil solution, applied for 30 days. The patient was directed to use this combination 5 days per week for 6 weeks. The specified dosage for each medication was a fifth of a packet of imiquimod 5% cream, an equivalent amount of tazarotene 0.1% cream, and a single drop of 5-fluorouracil 2% solution. These were combined on a bandage and placed on the lesion overnight. Following the treatment, a 3-week post-application examination revealed an erosion, 1.0 cm × 0.9 cm, amidst erythema. A subsequent incisional biopsy with histopathology and stains for CD10 and CD99, 3 weeks after treatment, and three punch biopsies with histopathology and stains for CD10 and CD99, 1-year post-treatment, confirmed the absence of AFX. AFX is a superficial variant of pleomorphic dermal sarcoma (PDS), which shares histologic similarities, yet the exact relationship between AFX/PDS and undifferentiated pleomorphic sarcoma is still not well understood. Previous studies have indicated a genomic similarity between AFX/PDS and cutaneous squamous cell carcinoma (cSCC), which suggests the potential efficacy of cSCC-targeted treatments for AFX/PDS. This case marks the first recorded instance of successful topical medical treatment of AFX, offering an alternative for patients who may opt out of surgical intervention. Continued research to assess the broader efficacy of this approach is encouraged.

摘要

本病例报告描述了一名80岁男性,其右颞部出现一个不断增大的伴有糜烂的红斑结节,大小为0.6厘米×0.6厘米。该病变后来被诊断为非典型纤维黄色瘤(AFX)。由于手术切除和修复的相关费用,患者未选择金标准治疗方法——莫氏手术,而是选择了局部治疗方案。该局部治疗方案包括他扎罗汀乳膏、咪喹莫特乳膏和5-氟尿嘧啶溶液,应用30天。患者被指示每周使用该组合5天,持续6周。每种药物的指定剂量为一包5%咪喹莫特乳膏的五分之一、等量的0.1%他扎罗汀乳膏以及一滴2% 5-氟尿嘧啶溶液。将这些药物混合在绷带上,敷于病变部位过夜。治疗后,用药3周后的检查显示在红斑中有一个1.0厘米×0.9厘米的糜烂。治疗3周后进行的一次切开活检及CD10和CD99染色,以及治疗1年后进行的三次打孔活检及CD10和CD99染色,均证实不存在AFX。AFX是多形性皮肤肉瘤(PDS)的一种浅表变体,两者在组织学上有相似之处,但AFX/PDS与未分化多形性肉瘤的确切关系仍未完全明确。先前的研究表明AFX/PDS与皮肤鳞状细胞癌(cSCC)之间存在基因组相似性,这表明针对cSCC的治疗方法可能对AFX/PDS有效。本病例是AFX成功局部药物治疗的首例记录,为可能选择不进行手术干预的患者提供了一种替代方案。鼓励继续开展研究以评估该方法的更广泛疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b408/11052744/35838a19c3af/13555_2024_1127_Fig1_HTML.jpg

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