Discipline of Ophthalmology, Department of Surgery II, Discipline of Anatomy and Embryology, Department of Morphofunctional Sciences I, Faculty of Medicine, Grigore T. Popa University of Medicine and Pharmacy, Iaşi, Romania;
Rom J Morphol Embryol. 2021 Oct-Dec;62(4):907-915. doi: 10.47162/RJME.62.4.03.
Conjunctival pigmented neoplasia can be benign, premalignant or malignant tumors. Our study aims to establish the epidemiological, gross morphological and immunohistopathological features of the conjunctival pigmented lesions in pediatric and adolescent patients (<18 years), to establish an accurate diagnosis.
PATIENTS, MATERIAL AND METHODS: This is a retrospective case series study conducted within two Ophthalmology Clinics from Iaşi, Romania, on seven pediatric and adolescent patients. Using the Clinical Observation Chart and the Pathology Registers over a six-years period (January 2015-December 2021), we noted the patients' demographic data, clinical data, and ophthalmological investigations of the lesion, as well as the type of their treatment. All histological sections stained with Hematoxylin-Eosin (HE) and with five antibodies [pan-cytokeratin (pan-CK) AE1∕AE3, S100 protein, Melan A, human melanoma black 45 (HMB45), and Ki67] were re-examined by four pathologists for each case, to identify the type of the conjunctival lesion and its histological and immunohistochemical features.
The mean age of all patients was 10.28 years, and the female∕male ratio was 1.3. Right eye was more often affected (71.42%). 71.42% of cases presented an elevated lesion, 57.14% of cases showed a lightly pigmented lesion, but 14.28% of cases exhibited a pink lesion and this feature described the inflamed juvenile conjunctival nevus. In all cases (100%) the conjunctival pigmented tumor was removed with safety margins. The microscopic examination revealed a compound melanocytic nevus in 57.14% cases, a junctional conjunctival nevus in 14.28% cases, an inflamed juvenile nevus in 14.28% cases, and a conjunctival melanoma arising from a pre-existing nevus in 14.28% cases. In all cases of nevi, the nevoid melanocytes showed strong immunopositivity for Melan A and S100 protein, variable and weak immunopositivity for HMB45, and a mean Ki67 labeling index of 1.71%. Conjunctival melanoma revealed strong immunopositivity of tumor cells for HMB45, Melan A and S100 protein, and a Ki67 labeling index of 20%. In all cases, the conjunctival epithelium showed strong immunopositivity for pan-CK AE1∕AE3. All our cases (100%) had a favorable outcome after the surgical removal of the tumor.
Any excision of a conjunctival pigmented lesion must be subject to a systematic immunohistopathological examination, and there is a set of antibodies (anti-HMB45 and anti-Ki67) that are useful for differential diagnosis between a conjunctival nevus and a conjunctival melanoma.
结膜色素性肿瘤可为良性、癌前或恶性肿瘤。本研究旨在建立儿科和青少年患者(<18 岁)结膜色素病变的流行病学、大体形态学和免疫组织病理学特征,以做出准确诊断。
患者、材料和方法:这是一项在罗马尼亚雅西的两个眼科诊所进行的回顾性病例系列研究,纳入了 7 名儿科和青少年患者。通过临床观察表和病理学登记册,我们记录了患者的人口统计学数据、临床数据以及病变的眼科检查结果,以及他们的治疗类型。所有组织学切片均用苏木精-伊红(HE)染色,并使用五种抗体[泛细胞角蛋白(pan-CK)AE1∕AE3、S100 蛋白、Melan A、人黑色素瘤黑 45(HMB45)和 Ki67]进行重新检查,由四位病理学家对每个病例进行检查,以确定结膜病变的类型及其组织学和免疫组织化学特征。
所有患者的平均年龄为 10.28 岁,女性与男性的比例为 1.3。右眼更常受累(71.42%)。71.42%的病例表现为隆起性病变,57.14%的病例表现为轻度色素性病变,但 14.28%的病例表现为粉红色病变,这一特征描述了炎症性青少年结膜痣。所有(100%)结膜色素性肿瘤均安全切除。显微镜下检查显示,57.14%的病例为复合性黑色素细胞痣,14.28%的病例为交界性结膜痣,14.28%的病例为炎症性青少年痣,14.28%的病例为源于先前存在痣的结膜黑色素瘤。在所有痣中,痣细胞对 Melan A 和 S100 蛋白表现出强烈的免疫阳性,对 HMB45 的免疫阳性程度可变且较弱,Ki67 标记指数平均为 1.71%。结膜黑色素瘤显示肿瘤细胞对 HMB45、Melan A 和 S100 蛋白的强烈免疫阳性,Ki67 标记指数为 20%。所有病例的结膜上皮均对 pan-CK AE1∕AE3 表现出强烈的免疫阳性。我们所有的病例(100%)在肿瘤切除后均获得良好的结果。
任何结膜色素性病变的切除都必须进行系统的免疫组织病理学检查,有一组抗体(抗 HMB45 和抗 Ki67)对结膜痣和结膜黑色素瘤的鉴别诊断很有用。