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派杰样黑素细胞增多症:是误诊还是警钟?

Pagetoid melanocytosis: tease or tocsin?

作者信息

Stern J B, Haupt H M

机构信息

Laboratory of Pathology, National Institutes of Health, Bethesda, MD, USA.

出版信息

Semin Diagn Pathol. 1998 Aug;15(3):225-9.

PMID:9711673
Abstract

Pagetoid melanocytosis (PM) represents a more precise formulation of the histological phenomenon previously referred to as pagetoid scatter/spread. PM is defined as the upward discontinuous extension of melanocytes into the superficial epidermis. Three histological criteria are presented. PM is a frequent finding in malignant melanoma, occurring in approximately 76% of lesions. PM also occurs in a significant number of certain benign melanocytic lesions: Spitz nevi, nevi of palms and soles, pigmented spindle cell nevi, recurrent nevi, vulvar nevi, and nevi of infancy and childhood. Histological features of PM favoring malignant melanoma over benign melanocytic lesions are a diffuse and dense extension over a wide area, prominent melanocytic atypia, and PM without an underlying junctional melanocytic component (free-floating PM). PM should alert the pathologist to the possibility of melanoma but does not of necessity require a malignant interpretation. The final interpretation of a melanocytic lesion requires evaluation of all the pertinent histological and clinical findings.

摘要

派杰样黑素细胞增多症(PM)是对先前称为派杰样散布/播散的组织学现象更精确的表述。PM被定义为黑素细胞向上间断性延伸至表皮浅层。文中提出了三项组织学标准。PM在恶性黑色素瘤中很常见,约76%的病变中会出现。PM也在相当数量的某些良性黑素细胞性病变中出现:斯皮茨痣、掌跖痣、色素性梭形细胞痣、复发性痣、外阴痣以及婴幼儿痣。相较于良性黑素细胞性病变,PM中提示恶性黑色素瘤的组织学特征包括在广泛区域的弥漫性致密延伸、显著的黑素细胞异型性以及无潜在交界性黑素细胞成分的PM(游离性PM)。PM应提醒病理学家注意黑色素瘤的可能性,但不一定需要作出恶性的诊断。对黑素细胞性病变的最终诊断需要评估所有相关的组织学和临床发现。

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