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Buschke-Lowenstein肿瘤:综述与拟议的分类系统

Buschke-Lowenstein Tumors: A Review and Proposed Classification System.

作者信息

Davis Kurt G, Barton Jeffrey S, Orangio Guy, Bivin William, Krane Spencer

机构信息

From the Departments of Surgery.

Pathology, LSU School of Medicine.

出版信息

Sex Transm Dis. 2021 Dec 1;48(12):e263-e268. doi: 10.1097/OLQ.0000000000001437.

DOI:10.1097/OLQ.0000000000001437
PMID:33833150
Abstract

Buschke-Lowenstein (B-L) tumors or giant condylomata are large fungating lesions that are caused by human papillomavirus (HPV) and develop in the anogenital region. Although uncommon, physicians and surgeons who treat sexually transmitted diseases or other diseases involving the anogenital area will encounter these patients. The purpose of this study is to review the current literature regarding these lesions. We evaluated every published study in PubMed and Embase from 1925 to 2020, concentrating on the clinical data included in each report, such as presentation and treatment. We also evaluated each work for any definition used and found that there is no accepted definition for these lesions. As such, we provide an inclusive, workable definition. In addition, there are many misconceptions about B-L that continue to be propogated as more case reports are published every year. After evaluating every published case, we refute the fact that these lesions have a high mortality or a high malignancy rate. Furthermore, we refute that these lesions are synonymous with verrucous carcinoma. In addition to a definition, we also propose a simple grading system that we hope can be used to assist in the study and management of these patients moving forward. Although the literature is very heterogenous regarding B-L, they are caused by HPV and are distinct from verrucous carcinoma. Because of the majority of information is based on case reports, the literature concentrates on treatment, but more work is clearly needed to delineate the association with specific HPV types and optimal management of this disease.

摘要

Buschke-Lowenstein(B-L)肿瘤或巨大尖锐湿疣是由人乳头瘤病毒(HPV)引起的、发生于肛门生殖器区域的巨大蕈样病变。虽然不常见,但治疗性传播疾病或其他累及肛门生殖器区域疾病的内科医生和外科医生会遇到这类患者。本研究的目的是回顾关于这些病变的现有文献。我们评估了1925年至2020年PubMed和Embase上发表的每一项研究,重点关注每份报告中包含的临床数据,如临床表现和治疗方法。我们还评估了各项研究中使用的任何定义,发现对于这些病变没有公认的定义。因此,我们提供了一个全面、可行的定义。此外,随着每年发表的病例报告越来越多,关于B-L仍存在许多误解并持续传播。在评估了每一篇已发表的病例后,我们反驳了这些病变具有高死亡率或高恶性率这一事实。此外,我们反驳了这些病变与疣状癌同义的说法。除了一个定义外,我们还提出了一个简单的分级系统,希望可用于协助今后对这些患者的研究和管理。尽管关于B-L的文献非常参差不齐,但它们由HPV引起,且与疣状癌不同。由于大多数信息基于病例报告,文献主要集中在治疗方面,但显然需要更多工作来阐明与特定HPV类型的关联以及该疾病的最佳管理方法。

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1
Buschke-Lowenstein Tumors: A Review and Proposed Classification System.Buschke-Lowenstein肿瘤:综述与拟议的分类系统
Sex Transm Dis. 2021 Dec 1;48(12):e263-e268. doi: 10.1097/OLQ.0000000000001437.
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Rearrangements of the upstream regulatory region of human papillomavirus type 6 can be found in both Buschke-Löwenstein tumours and in condylomata acuminata.人乳头瘤病毒6型上游调控区的重排可见于Buschke-Löwenstein肿瘤和尖锐湿 疣中。
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[A case of giant condyloma acuminatum. On differential diagnosis of giant condylomas from Buschke-Löwenstein tumors and verrucous carcinoma].[一例巨大尖锐湿疣。关于巨大尖锐湿疣与Buschke-Löwenstein肿瘤及疣状癌的鉴别诊断]
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Anal verrucous carcinoma is not related to infection with human papillomaviruses and should be distinguished from giant condyloma (Buschke-Löwenstein tumour).肛管疣状癌与人类乳头瘤病毒感染无关,应与巨大尖锐湿疣(Buschke-Löwenstein瘤)相鉴别。
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Comprehensive analysis of human papillomavirus prevalence and the potential role of low-risk types in verrucous carcinoma.人乳头瘤病毒流行情况的综合分析及低危型别在疣状癌中潜在作用。
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[Buschke-Lowenstein tumors].[Buschke-Löwenstein肿瘤]
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Buschke-Löwenstein Tumor: An Unusual Therapeutic Approach.Buschke-Löwenstein瘤:一种不寻常的治疗方法。
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Medicine (Baltimore). 2025 Jun 6;104(23):e42798. doi: 10.1097/MD.0000000000042798.
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J Surg Case Rep. 2024 Jul 12;2024(7):rjae459. doi: 10.1093/jscr/rjae459. eCollection 2024 Jul.
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Remission of HPV-Related Diseases by Antivirals for Herpesvirus: Clinical Cases and a Literature Review.抗病毒药物治疗疱疹病毒相关疾病的缓解:临床病例及文献复习。
Viruses. 2024 May 10;16(5):756. doi: 10.3390/v16050756.
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[Anogenital warts-An update].[肛门生殖器疣——最新进展]
Dermatologie (Heidelb). 2024 Jan;75(1):30-39. doi: 10.1007/s00105-023-05282-8. Epub 2023 Dec 18.
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BMJ Case Rep. 2023 Oct 3;16(10):e255996. doi: 10.1136/bcr-2023-255996.
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