Harvell J D, Meehan S A, LeBoit P E
Department of Pathology, University of California, San Francisco, School of Medicine, 94143-0506, USA.
J Cutan Pathol. 1997 Nov;24(10):611-9. doi: 10.1111/j.1600-0560.1997.tb01092.x.
Halo reactions to melanocytic nevi are a well-recognized phenomenon. In contrast, halo reactions to Spitz's nevi have been reported only infrequently. Halo reactions may cause misdiagnosis of an otherwise benign nevus as melanoma because inflammatory cells sometimes obscure the architectural features of the underlying nevus, and may induce cytologic atypia. For Spitz's nevus where the distinction between malignancy and benignancy is already challenging, halo reactions compound the problem. We describe 17 examples of Spitz's nevus with halo reaction, and compare their immunohistochemical features with those of "ordinary" halo nevi. Only 2 of 17 lesions demonstrated clinically apparent halos. Clinical follow-up was available for 12 of 17 cases. None of the 12 has persisted at the biopsy site or metastasized after an average 3.6-year follow-up period. Junctional, compound, intradermal, and combined types of Spitz's nevi were represented. All were characterized by symmetrical lymphocytic infiltrates which permeated the full thickness of the nevus, including junctional nests. Combined Spitz's nevi constituted more than one-half of examples in this series (9/17 cases). The combined Spitz's nevus included a combination of Spitz's nevus with either an ordinary (common, banal) nevus or a superficial congenital type nevus. In these combined Spitz's nevi, the lymphocytic response was often directed exclusively to the Spitz's nevic component. Important distinguishing features from malignant melanoma arising in a pre-existing nevus included symmetry and lateral circumscription of the spitzoid component, no large expansile-appearing aggregates of melanocytes, a decrease in size of nests with increasing dermal depth, a lack of mitotic figures among melanocytes at the base, and a symmetrical and diffusely permeative lymphocytic response. Although the combined Spitz's nevus with halo reaction sometimes appeared asymmetrical at scanning magnification, each component of the combination was symmetrical, when examined independently. Probably because of reactive atypia, nuclear maturation with progressive descent into the dermis was sometimes absent. There were no obvious differences in immunohistochemical staining patterns among 4 Spitz's nevi with halo reaction, 5 regressing melanomas, and 5 benign halo nevi when stained with antibodies to S100, HMB-45, OPD4, CD8, TIA-1, CD1a, CD68, and Ki-67.
黑素细胞痣的晕痣反应是一种广为人知的现象。相比之下,Spitz痣的晕痣反应仅有罕见报道。晕痣反应可能会将原本良性的痣误诊为黑色素瘤,因为炎症细胞有时会掩盖其下方痣的结构特征,并可能导致细胞非典型性。对于Spitz痣而言,其良恶性鉴别本就具有挑战性,晕痣反应更是雪上加霜。我们描述了17例伴有晕痣反应的Spitz痣,并将其免疫组化特征与“普通”晕痣的特征进行比较。17个病变中仅2个有临床明显的晕。17例中有12例有临床随访资料。平均3.6年的随访期后,这12例中无一例在活检部位持续存在或发生转移。包括交界型、复合型、皮内型及混合型的Spitz痣均有代表。所有病例均以对称的淋巴细胞浸润为特征,浸润贯穿痣的全层,包括交界巢。混合型Spitz痣占本系列病例的一半以上(9/17例)。混合型Spitz痣包括Spitz痣与普通(常见、平凡)痣或浅表先天性痣的组合。在这些混合型Spitz痣中,淋巴细胞反应通常仅针对Spitz痣成分。与在原有痣基础上发生的恶性黑色素瘤的重要鉴别特征包括:Spitz样成分的对称性和侧向边界、无大的呈扩张状的黑素细胞聚集、随着真皮深度增加巢的大小减小、基底部黑素细胞中无核分裂象以及对称且弥漫性浸润的淋巴细胞反应。尽管伴有晕痣反应的混合型Spitz痣在低倍镜下有时看似不对称,但各组成部分单独检查时均是对称的。可能由于反应性非典型性,有时缺乏随着向真皮深层逐渐下降的核成熟现象。用S100、HMB - 45、OPD4、CD8、TIA - 1、CD1a、CD68和Ki - 67抗体染色时,4例伴有晕痣反应的Spitz痣、5例消退期黑色素瘤和5例良性晕痣在免疫组化染色模式上无明显差异。