Physician, Dermatology Unit, Galliera Hospital, Genova, Italy.
Physician, Skin Cancer Unit, Istituto Scientifico Romagnolo per lo Studio dei Tumori (IRST) IRCCS, Meldola, Italy.
Am J Dermatopathol. 2023 Mar 1;45(3):153-162. doi: 10.1097/DAD.0000000000002323. Epub 2022 Nov 7.
Spark's nevus is a particular type of melanocytic nevus, with histology that shows features of both Spitz and Clark nevus. Detailed dermoscopic features in a series of Spark nevi have not been described yet. We performed a monocentric retrospective observational study on 20 lesions of Spark nevus excised from 19 patients (M:F = 10:9; mean age: 37,6 years), reviewed by 5 experts in dermoscopy and 2 dermatopathologists. A histologic review confirmed that Spark nevi were mostly symmetric (80%), well circumscribed (100%), mainly compound (65%) melanocytic lesions with either epithelioid (55%) or spitzoid (45%) cell morphology and bridging of the nests (100%). Spark nevi were more frequently found on the trunk (85%) in patients with a history of sunburns in childhood (84%), with skin phototype III (79%), and with high nevus count (>100 nevi, 7 patients (36%)). On dermoscopy, we observed different general patterns: multicomponent (40%), reticular-globular-homogeneous (15%), globular homogeneous (15%), reticular (15%), reticular-globular (5%), homogeneous (5%), and globular (5%). Spark nevi showed frequently dermoscopic asymmetry (63%), brown color (90%) with areas of central hyperpigmentation (41%) and peripheral hypopigmentation (28%), atypical pigment network (48%), irregular globules (42%), irregular dots (31%), irregular blotches (16%), blue-whitish veil (13%), peripheral island (25%), irregular hyperpigmented areas (12%), and regression (33%). BRAF mutation was present in 7 of the 10 analyzed cases (70%); all these cases presented a history of evolution. In conclusion, Spark nevi occur on the trunk of young adults with high nevus count and history of sunburns; dermoscopic features are protean, often atypical and suspicious of melanoma.
斯帕克痣是一种特殊类型的黑色素细胞痣,其组织学表现兼有 Spitz 痣和 Clark 痣的特征。尚未描述一系列斯帕克痣的详细皮肤镜特征。我们对 19 名患者(男女比为 10:9;平均年龄 37.6 岁)的 20 个斯帕克痣病变进行了一项单中心回顾性观察研究,这些病变由 5 名皮肤镜专家和 2 名皮肤病理学家进行了回顾。组织学回顾证实,斯帕克痣主要为对称性(80%)、边界清楚(100%)、主要为复合(65%)黑色素细胞病变,具有上皮样(55%)或斯皮茨样(45%)细胞形态和巢桥接(100%)。斯帕克痣更多见于躯干(85%),患者有儿童期晒伤史(84%),皮肤光型为 III 型(79%),痣计数高(>100 个痣,7 例(36%))。在皮肤镜下,我们观察到不同的一般模式:多成分(40%)、网状-球形-均匀(15%)、球形均匀(15%)、网状(15%)、网状-球形(5%)、均匀(5%)和球形(5%)。斯帕克痣常表现为皮肤镜下不对称(63%)、棕色(90%),伴有中央色素沉着(41%)和周围色素减退(28%)、非典型色素网(48%)、不规则球形(42%)、不规则点(31%)、不规则斑片(16%)、蓝白色面纱(13%)、周围岛(25%)、不规则色素沉着区(12%)和退化(33%)。在分析的 10 例中,有 7 例(70%)存在 BRAF 突变;所有这些病例均有进展史。总之,斯帕克痣发生于躯干,多见于有大量痣和晒伤史的年轻成年人;皮肤镜特征多样,常为非典型,提示黑色素瘤。