{"title":"外阴非硬化性苔癣:临床病理分析。","authors":"Anne K Bartels, Oluwole Fadare","doi":"10.1097/PGP.0000000000001065","DOIUrl":null,"url":null,"abstract":"<p><p>The International Society of the Study of Vulvovaginal Diseases (ISSVD) recently defined nonsclerotic lichen sclerosus (NSLS) as a scenario wherein the clinical findings are consistent with lichen sclerosus (LS), but no microscopic evidence of dermal sclerosis is found and recognized 4 histologic subcategories. Herein, we present an institutional experience with NSLS, with an emphasis on frequency, application of the ISSVD categories in routine practice, and clinicopathologic correlation. The authors reviewed clinical and pathologic findings for consecutive vulvar biopsies in which LS was a clinical and/or pathologic consideration. Cases were classified as classical/sclerotic LS (CLS), NSLS (per ISSVD criteria), and \"unclassified,\" the latter of which were cases not classifiable as NSLS or CLS, despite a clinical impression or LS or LS being a significant clinical consideration (ie, \"clinical LS\"). In clinical LS cases, CLS and NSLS were diagnosed histologically in 61% (182/298) and 15% (44/298), respectively, whereas the remainder were histologically unclassified. The latter group was microscopically heterogeneous, devoid of a consistent pathologic profile, and generally showed absence, focality, minimality, ambiguity, or infrequency of features that would have allowed their categorization into one of the NSLS categories. Among the 4 categories for the categorizable NSLS cases, the \"lichenoid dermatitis\" pattern (61.4%) was the commonest, followed by dermal fibrosis with acanthosis (22.7%), dermal fibrosis without acanthosis (9.1%), and hypertrophic lichenoid dermatitis (6.8%). The clinical response rates to topical therapies for the NSLS and unclassified groups were 71% and 62%, respectively (P=0.4). Our findings highlight the significance of clinicopathologic correlation in the diagnosis of NSLS. In the setting of clinical LS, some histologic evidence to support that impression is found in most cases when the ISSVD system for diagnosis and classification of biopsies is applied. However, a subset of clinical LS cases are not pathologically classifiable as either CLS or any of the NSLS categories; these display nonspecific histologic features and require future study.</p>","PeriodicalId":14001,"journal":{"name":"International Journal of Gynecological Pathology","volume":" ","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nonsclerotic Lichen Sclerosus of Vulva: A Clinicopathologic Analysis.\",\"authors\":\"Anne K Bartels, Oluwole Fadare\",\"doi\":\"10.1097/PGP.0000000000001065\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The International Society of the Study of Vulvovaginal Diseases (ISSVD) recently defined nonsclerotic lichen sclerosus (NSLS) as a scenario wherein the clinical findings are consistent with lichen sclerosus (LS), but no microscopic evidence of dermal sclerosis is found and recognized 4 histologic subcategories. Herein, we present an institutional experience with NSLS, with an emphasis on frequency, application of the ISSVD categories in routine practice, and clinicopathologic correlation. The authors reviewed clinical and pathologic findings for consecutive vulvar biopsies in which LS was a clinical and/or pathologic consideration. Cases were classified as classical/sclerotic LS (CLS), NSLS (per ISSVD criteria), and \\\"unclassified,\\\" the latter of which were cases not classifiable as NSLS or CLS, despite a clinical impression or LS or LS being a significant clinical consideration (ie, \\\"clinical LS\\\"). In clinical LS cases, CLS and NSLS were diagnosed histologically in 61% (182/298) and 15% (44/298), respectively, whereas the remainder were histologically unclassified. The latter group was microscopically heterogeneous, devoid of a consistent pathologic profile, and generally showed absence, focality, minimality, ambiguity, or infrequency of features that would have allowed their categorization into one of the NSLS categories. Among the 4 categories for the categorizable NSLS cases, the \\\"lichenoid dermatitis\\\" pattern (61.4%) was the commonest, followed by dermal fibrosis with acanthosis (22.7%), dermal fibrosis without acanthosis (9.1%), and hypertrophic lichenoid dermatitis (6.8%). The clinical response rates to topical therapies for the NSLS and unclassified groups were 71% and 62%, respectively (P=0.4). Our findings highlight the significance of clinicopathologic correlation in the diagnosis of NSLS. In the setting of clinical LS, some histologic evidence to support that impression is found in most cases when the ISSVD system for diagnosis and classification of biopsies is applied. 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引用次数: 0
摘要
国际外阴疾病研究学会(ISSVD)最近将非硬化性苔藓硬化症(NSLS)定义为临床表现与苔藓硬化症(LS)一致,但显微镜下未发现真皮硬化的证据,并确认了 4 个组织学亚类。在此,我们介绍了一家机构在 NSLS 方面的经验,重点是频率、ISSVD 分类在常规实践中的应用以及临床病理相关性。作者回顾了以 LS 为临床和/或病理考虑因素的连续外阴活检的临床和病理结果。病例被分为经典/硬化性LS(CLS)、NSLS(根据ISSVD标准)和 "未分类",后者是指尽管临床印象或LS或LS是一个重要的临床考虑因素(即 "临床LS"),但无法归类为NSLS或CLS的病例。在临床LS病例中,经组织学诊断为CLS和NSLS的分别占61%(182/298)和15%(44/298),而其余病例则未经组织学分类。后者在显微镜下表现为异质性,没有一致的病理特征,通常表现为缺乏、病灶性、微小性、模糊性或不常见特征,而这些特征本可将其归入 NSLS 的某个类别。在可归类的 NSLS 病例的 4 个类别中,"苔癣样皮炎 "模式(61.4%)最常见,其次是伴有棘皮症的真皮纤维化(22.7%)、不伴有棘皮症的真皮纤维化(9.1%)和肥厚性苔癣样皮炎(6.8%)。NSLS组和未分级组对局部疗法的临床反应率分别为71%和62%(P=0.4)。我们的研究结果凸显了临床病理相关性在诊断 NSLS 中的重要性。在临床 LS 的情况下,应用 ISSVD 系统对活检组织进行诊断和分类时,大多数病例都能找到一些组织学证据来支持这种印象。然而,有一部分临床 LS 病例在病理上无法归类为 CLS 或任何 NSLS 类别;这些病例显示出非特异性组织学特征,需要在未来进行研究。
Nonsclerotic Lichen Sclerosus of Vulva: A Clinicopathologic Analysis.
The International Society of the Study of Vulvovaginal Diseases (ISSVD) recently defined nonsclerotic lichen sclerosus (NSLS) as a scenario wherein the clinical findings are consistent with lichen sclerosus (LS), but no microscopic evidence of dermal sclerosis is found and recognized 4 histologic subcategories. Herein, we present an institutional experience with NSLS, with an emphasis on frequency, application of the ISSVD categories in routine practice, and clinicopathologic correlation. The authors reviewed clinical and pathologic findings for consecutive vulvar biopsies in which LS was a clinical and/or pathologic consideration. Cases were classified as classical/sclerotic LS (CLS), NSLS (per ISSVD criteria), and "unclassified," the latter of which were cases not classifiable as NSLS or CLS, despite a clinical impression or LS or LS being a significant clinical consideration (ie, "clinical LS"). In clinical LS cases, CLS and NSLS were diagnosed histologically in 61% (182/298) and 15% (44/298), respectively, whereas the remainder were histologically unclassified. The latter group was microscopically heterogeneous, devoid of a consistent pathologic profile, and generally showed absence, focality, minimality, ambiguity, or infrequency of features that would have allowed their categorization into one of the NSLS categories. Among the 4 categories for the categorizable NSLS cases, the "lichenoid dermatitis" pattern (61.4%) was the commonest, followed by dermal fibrosis with acanthosis (22.7%), dermal fibrosis without acanthosis (9.1%), and hypertrophic lichenoid dermatitis (6.8%). The clinical response rates to topical therapies for the NSLS and unclassified groups were 71% and 62%, respectively (P=0.4). Our findings highlight the significance of clinicopathologic correlation in the diagnosis of NSLS. In the setting of clinical LS, some histologic evidence to support that impression is found in most cases when the ISSVD system for diagnosis and classification of biopsies is applied. However, a subset of clinical LS cases are not pathologically classifiable as either CLS or any of the NSLS categories; these display nonspecific histologic features and require future study.
期刊介绍:
International Journal of Gynecological Pathology is the official journal of the International Society of Gynecological Pathologists (ISGyP), and provides complete and timely coverage of advances in the understanding and management of gynecological disease. Emphasis is placed on investigations in the field of anatomic pathology. Articles devoted to experimental or animal pathology clearly relevant to an understanding of human disease are published, as are pathological and clinicopathological studies and individual case reports that offer new insights.