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阴茎鳞状细胞癌患者中硬化性苔藓的高发病率。

High incidence of lichen sclerosus in patients with squamous cell carcinoma of the penis.

作者信息

Powell J, Robson A, Cranston D, Wojnarowska F, Turner R

机构信息

Department of Dermatology, The Churchill, Old Road, Headington, Oxford OX3 7LJ, UK.

出版信息

Br J Dermatol. 2001 Jul;145(1):85-9. doi: 10.1046/j.1365-2133.2001.04287.x.

Abstract

BACKGROUND

There is a well-documented association between lichen sclerosus (LS) and vulval carcinoma in women; however, until recently, there have only been anecdotal reports of penile squamous cell carcinoma (SCC) occurring in men with LS.

OBJECTIVE

The incidence of penile carcinoma occurring on a background of LS remains uncertain, and we wished to examine this possible association further.

METHOD

To address this, all the cases (n = 20) of penile SCC held on our pathology database (4 years) were examined. Histology was reviewed, blind to the clinical picture, for evidence of LS, applying strict histological criteria. Subsequently, clinical notes were reviewed for history of LS before the SCC presented, and history of previous circumcision, treatments, node involvement, metastases and death.

RESULTS

In eight cases, evidence of LS was found in the excision specimen. Seven of these had well-differentiated SCC. In the 12 cases with no evidence of LS, only three were well differentiated. With case note review, seven had a history of LS (four with histological LS), sometimes preceding the SCC by 10 years. These all had well-differentiated SCC. Ten of the 20 patients are dead, seven from metastatic disease. Four deaths occurred in the 'well-differentiated LS' group, but only one from penile SCC metastatic disease.

CONCLUSIONS

There appears to be a definite association between SCC of the penis and the presence of LS, similar to that reported between LS and vulval SCC in women. Of the 20 patients with penile SCC studied, 11 had a clinical history and/or histological evidence of LS. However, clinical presentation of the LS or need for circumcision may precede the SCC by many years. As follow-up is impractical, counselling at the time of diagnosis is very important, and it is essential that medical practitioners are aware of this association so that the subsequent risk from SCC is reduced.

摘要

背景

女性外阴硬化性苔藓(LS)与外阴癌之间的关联已有充分记录;然而,直到最近,仅有关于患有LS的男性发生阴茎鳞状细胞癌(SCC)的零星报道。

目的

在LS背景下发生阴茎癌的发病率仍不确定,我们希望进一步研究这种可能的关联。

方法

为解决此问题,我们检查了病理数据库中保存的所有阴茎SCC病例(共20例,时间跨度为4年)。在对临床情况不知情的情况下,依据严格的组织学标准复查组织学切片,以寻找LS的证据。随后,查阅临床记录,了解SCC出现之前的LS病史、既往包皮环切术史、治疗史、淋巴结受累情况、转移情况及死亡情况。

结果

在8例病例的切除标本中发现了LS的证据。其中7例为高分化SCC。在12例无LS证据的病例中,只有3例为高分化。通过病例记录复查,7例有LS病史(4例有组织学证实的LS),有时在SCC出现前10年就已存在。这些病例均为高分化SCC。20例患者中有10例死亡,7例死于转移性疾病。4例死亡发生在“高分化LS”组,但仅1例死于阴茎SCC转移性疾病。

结论

阴茎SCC与LS之间似乎存在明确关联,类似于女性LS与外阴SCC之间的关联。在所研究的20例阴茎SCC患者中,11例有LS的临床病史和/或组织学证据。然而,LS的临床表现或包皮环切术需求可能在SCC出现前许多年就已存在。由于随访不切实际,诊断时的咨询非常重要,医生必须了解这种关联,以便降低后续SCC的风险。

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