Sugiura Mitsuhiro, Colby Kathryn A, Mihm Martin C, Zembowicz Artur
Department of Pathology, Massachusetts General Hospital Harvard Medical School, Boston, MA, USA.
Am J Surg Pathol. 2007 Feb;31(2):185-92. doi: 10.1097/01.pas.0000213339.32734.64.
The current World Health Organization classification of conjunctival melanocytic proliferations divides them into conjunctival nevi and invasive melanoma but, in contrast to other anatomic sites, does not recognize melanoma in situ. All atypical intraepithelial conjunctival proliferations are included in a heterogeneous category designated as primary acquired melanosis (PAM) with atypia. We performed clinicopathologic analysis of 29 cases of PAM with atypia. On the basis of histologic features and frequency of association with invasive melanoma and metastases, we were able to divide our cases into 2 histologic groups. The low-risk group (13 cases) included lesions composed of small to medium size melanocytes with high nuclear to cytoplasmic ratio and small to medium size hyperchromatic nuclei devoid of nucleoli showing predominantly single cell lentiginous growth pattern. Invasive melanoma occurred in only 2 cases from this group. None of these lesions metastasized. The second, high-risk group (16 cases), showed increased frequency of association with invasive melanoma (15/16 cases, 94%) and metastases (4/16 cases, 25%). These lesions were more heterogeneous architecturally but were all composed of melanocytes showing various degrees of epithelioid features such as abundant cytoplasm, vesicular nuclei, or prominent nucleoli. In 4 cases discrete areas showing high-risk and low-risk features were identified. All 4 lesions were associated with invasion. Our findings offer a practical approach for prognostically useful subclassification of PAM with atypia, which emphasizes cytologic features of intraepithelial conjunctival melanocytic proliferation.
世界卫生组织目前对结膜黑素细胞增生的分类将其分为结膜痣和浸润性黑色素瘤,但与其他解剖部位不同的是,不认可原位黑色素瘤。所有非典型上皮内结膜增生都被纳入一个异质性类别,称为非典型原发性获得性黑素沉着症(PAM)。我们对29例非典型PAM进行了临床病理分析。根据组织学特征以及与浸润性黑色素瘤和转移的关联频率,我们能够将病例分为两个组织学组。低风险组(13例)包括由小至中等大小的黑素细胞组成的病变,细胞核与细胞质比例高,核小至中等大小、深染且无核仁,主要呈单细胞雀斑样生长模式。该组仅有2例发生浸润性黑色素瘤。这些病变均未发生转移。第二个高风险组(16例)与浸润性黑色素瘤(15/16例,94%)和转移(4/16例,25%)的关联频率增加。这些病变在结构上更具异质性,但均由显示不同程度上皮样特征(如丰富的细胞质、泡状核或明显核仁)的黑素细胞组成。在4例中,发现了显示高风险和低风险特征的离散区域。所有4个病变均与浸润有关。我们的研究结果为非典型PAM的预后有用亚分类提供了一种实用方法,该方法强调结膜上皮内黑素细胞增生的细胞学特征。