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结膜黑色素细胞癌前病变和恶性病变的临床病理特征

Clinicopathologic characteristics of premalignant and malignant melanocytic lesions of the conjunctiva.

作者信息

Jakobiec F A, Folberg R, Iwamoto T

机构信息

Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston 02114.

出版信息

Ophthalmology. 1989 Feb;96(2):147-66. doi: 10.1016/s0161-6420(89)32920-4.

Abstract

Primary acquired melanosis (PAM), a disease that affects mostly middle-aged white patients, is predominantly a proliferative condition of the melanocytes that normally populate the conjunctival epithelium. Primary acquired melanosis without atypia (low risk for the development of melanoma) is typically created by increased numbers of melanocytes restricted to the basilar region of the epithelium without nuclear hyperchromasia or prominence of the nucleoli. Primary acquired melanosis with atypia, a formal precursor of melanoma, is characterized by the proliferation of small polyhedral cells, spindle cells, large dendritiform melanocytes, or epithelioid cells that may: remain restricted to the basilar region (basilar nests); form nests at all levels of the epithelium; spread individually to all levels of the epithelium (pagetoid extension); or proliferate in a sheet-like fashion approximating a melanoma in situ. Lesions composed of epithelioid cells or exhibiting intraepithelial pagetoid extension have, respectively, a 75 or 90% chance of eventuating in invasive melanoma. Primary acquired melanosis in an adult should not be confused with "a junctional nevus," which is almost always restricted to childhood. Invasive melanomas measuring less than 0.8 mm in thickness tend not to be associated with metastases; the tumor cells may be small polyhedral (in which case confusion with a compound nevus often arises), epithelioid, spindled, or ballooned. Nodules composed of spindle cells in part or in toto tend to have less metastatic potential at a given thickness measurement than comparable nodules composed of epithelioid or polyhedral cells. The clinical features, electron microscopic findings, and biologic principles underwriting clinical management are also presented.

摘要

原发性获得性黑变病(PAM)主要影响中年白人患者,主要是正常存在于结膜上皮的黑素细胞的增殖性疾病。无异型性的原发性获得性黑变病(黑色素瘤发生风险低)通常是由局限于上皮基底区域的黑素细胞数量增加所致,无核深染或核仁突出。异型性原发性获得性黑变病是黑色素瘤的正式前驱病变,其特征是小多面体细胞、梭形细胞、大的树枝状黑素细胞或上皮样细胞增殖,这些细胞可能:仍局限于基底区域(基底巢);在上皮各层形成巢;单个扩散至上皮各层(派杰样扩展);或以片状方式增殖,近似原位黑色素瘤。由上皮样细胞组成或表现为上皮内派杰样扩展的病变,分别有75%或90%的几率发展为浸润性黑色素瘤。成人的原发性获得性黑变病不应与“交界痣”相混淆,后者几乎总是局限于儿童期。厚度小于0.8mm的浸润性黑色素瘤往往不伴有转移;肿瘤细胞可能是小多面体细胞(这种情况下常与复合痣混淆)、上皮样细胞、梭形细胞或气球样细胞。在给定厚度测量下,部分或全部由梭形细胞组成的结节比由上皮样或多面体细胞组成的类似结节转移潜能更低。还介绍了临床特征、电子显微镜检查结果以及支持临床管理的生物学原理。

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