Barnhill R L, Roush G C, Duray P H
Department of Dermatology, Yale University School of Medicine, New Haven, CT.
Hum Pathol. 1990 Jan;21(1):51-8. doi: 10.1016/0046-8177(90)90075-g.
The dysplastic nevus in nonfamilial melanoma is a clinicopathologic entity consistently demonstrating an eightfold or greater association with malignant melanoma. The present report quantifies the relationship between nuclear atypia and 16 architectural and cytoplasmic features in 153 pigmented nevi removed from a similar number of patients with newly diagnosed nonfamilial melanoma. All lesions were evaluated by one dermatopathologist, and most lesions were reviewed by a second dermatopathologist. Nuclear atypia of nevomelanocytes was defined as at least three of the following: nuclear enlargement, pleomorphism, hyperchromatism, and prominent nucleoli easily observed throughout each lesion. Seventeen percent of the total nevi had such atypia. On univariate analysis, 11 parameters (lentiginous hyperplasia of the epidermis, basal melanocytic hyperplasia, junctional nest disarray, fusion [bridging] of theques, suprabasal melanocytes, lymphoid response, prominent vascularity, fibroplasia, abundant cytoplasm, "dusty" cytoplasm, and large melanin granules) showed an association with nuclear atypia (P less than .05). However, on multivariate analysis only five parameters continued to be important: basal melanocytic hyperplasia, junctional nest disarray, melanophages (inverse correlation), prominent vascularity, and large melanin granules. These data support the idea that multiple histopathologic characteristics, correlating objectively with nuclear atypia, are important for the diagnosis of dysplastic nevi. In our view, the minimal essential histologic criteria for dysplastic nevi based on these findings include nuclear atypia and abnormal patterns of intraepidermal nevomelanocytic proliferation (ie, basal melanocytic hyperplasia and/or junctional nest disarray).
非家族性黑色素瘤中的发育异常痣是一种临床病理实体,始终显示出与恶性黑色素瘤有八倍或更高的关联。本报告量化了从相似数量新诊断的非家族性黑色素瘤患者身上切除的153个色素痣中核异型性与16种结构和细胞质特征之间的关系。所有病变均由一位皮肤病理学家评估,大多数病变由另一位皮肤病理学家复查。痣黑素细胞的核异型性定义为以下至少三项:核增大、多形性、深染以及在每个病变中易于观察到的明显核仁。全部痣中有17%有这种异型性。单因素分析显示,11个参数(表皮的雀斑样增生、基底黑素细胞增生、交界巢紊乱、痣细胞融合[桥接]、基底层上方黑素细胞、淋巴样反应、显著血管形成、纤维组织增生、丰富的细胞质、“尘状”细胞质以及大的黑素颗粒)与核异型性相关(P小于0.05)。然而,多因素分析中只有五个参数仍然重要:基底黑素细胞增生、交界巢紊乱、噬黑素细胞(负相关)、显著血管形成以及大的黑素颗粒。这些数据支持这样一种观点,即多个与核异型性客观相关的组织病理学特征对于发育异常痣的诊断很重要。我们认为,基于这些发现,发育异常痣的最小基本组织学标准包括核异型性和表皮内痣黑素细胞增殖的异常模式(即基底黑素细胞增生和/或交界巢紊乱)。